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polidocanol

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Description

Polidocanol: An alkyl polyglycol ether of LAURYL ALCOHOL, chemically defined as an alcohol ethoxylate having an average alkyl chain of 12–14 carbon atoms, and an ethylene oxide chain of 9 ethylene oxide units. It is used as a detergent, and medically as a local anesthetic, and as a sclerosing agent for the treatment of ESOPHAGEAL AND GASTRIC VARICES and VARICOSE VEINS. [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

polidocanol : A hydroxypolyether that is nonaethylene glycol in which one of the terminal hydroxy functions is substituted by a lauryl (dodecyl) group. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID656641
CHEMBL ID1231723
CHEBI ID46859
SCHEMBL ID25580
MeSH IDM0053330

Synonyms (62)

Synonym
CHEMBL1231723
3055-99-0
polidocanol
nonaethylene glycol monododecyl ether, nonionic surfactant
NCGC00166290-01
nonaethylene glycol monolauryl ether
dodecyl nona ethylene glycol ether
CHEBI:46859 ,
3,6,9,12,15,18,21,24,27-nonaoxanonatriacontan-1-ol
nonaethylene glycol monododecyl ether
NCGC00166290-02
poele
2-[2-[2-[2-[2-[2-[2-[2-(2-dodecoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol
9043-30-5
genapol x-080
0awh8bfg9a ,
dtxsid5039721 ,
dtxcid3019721
tox21_112394
cas-3055-99-0
laureth-9
varithena
polidocanol [inn:dcf:jan]
c12-e9
dodecyl nonaoxyethylene ether
einecs 221-284-4
dodecylnonaoxyethylene glycol monoether
asclera
dodecylnonaglycol
peg-9 lauryl ether
macrogol 9 lauryl ether
DB06811
aethoxy-sklerol
SCHEMBL25580
tox21_112394_1
NCGC00166290-03
ONJQDTZCDSESIW-UHFFFAOYSA-N
mfcd00043375
AKOS028108701
SR-01000944476-1
sr-01000944476
F20806
J-018016
genapol(r) x-080
marlipal 24/90
10xbio
10xb-101
lauromacrogol 450
polyethylene glycol monolauryl ether (n=9)
nikkol bl-9ex
AMY22525
HY-108294
CS-0028163
nonaoxyethylene monododecyl ether
polidocanols
BS-51745
EN300-7457094
N1204
nonaethylene glycol monododecyl ether [for biochemical research]
lauromacrogol 400 (ep monograph)
lauromacrogol 400 (mart.)
polyoxyl 9 lauryl ether (usp-rs)

Research Excerpts

Overview

Polidocanol is an FDA-approved sclerosant indicated for treating uncomplicated spider veins and reticular veins in the lower extremities. It is a local anaesthetic and antipruritic compound used in the treatment of itching skin conditions such as eczema.

ExcerptReferenceRelevance
"Polidocanol is a safe sclerosing agent with anesthetic properties and minimal skin toxicity."( Polidocanol Sclerotherapy in Pyogenic Granulomas.
Khurana, A; Mathachan, SR, 2022
)
3.61
"Polidocanol is an FDA-approved treatment of incompetent great saphenous veins, accessory saphenous veins, and visible varicosities of the great saphenous vein system, but numerous other off-label dermatological applications have been reported."( Polidocanol: A Review of Off-Label Dermatologic Uses.
Bur, D; Nguyen, QD; Silapunt, S; Stender, C, 2022
)
3.61
"Polidocanol sclerotherapy is a relatively new approach for these patients."( HEmoRhoidal disease management with Band ligation versus polidocanol Sclerotherapy: a systematic review and meta-analysis (the HerBS Review).
Doumouras, A; Eskicioglu, C; Hong, D; Lee, Y; McKechnie, T; Patel, J; Sharma, S; Wu, K, 2023
)
1.88
"Polidocanol is an FDA-approved sclerosant indicated for treating uncomplicated spider veins and reticular veins in the lower extremities. "( Improper Potency and Impurities in Compounded Polidocanol
Amatangelo, L; Mann, M; Morrison, N; Munavalli, GS, 2019
)
2.21
"Polidocanol is a local anaesthetic and antipruritic compound that is used in the treatment of itching skin conditions such as eczema. "( Polidocanol inhibits cowhage - but not histamine-induced itch in humans.
Church, MK; Fluhr, JW; Hawro, T; Maurer, M; Mengeaud, V; Metz, M; Redoulès, D, 2014
)
3.29
"Polidocanol is a liquid surfactant having endothelial cell lytic properties. "( Polidocanol for endovenous microfoam sclerosant therapy.
Eckmann, DM, 2009
)
3.24
"Polidocanol is a useful sclerosing agent for treating testicular hydrocele. "( [Sclerotherapy of idiopatic hydrocele with polidocanol: a study about 190 cases].
Ben Rais, N; Ben Rhouma, S; Binous, MY; Chelif, M; Hmidi, M; Horchani, A; Nouira, Y; Sallami, S, 2011
)
2.07
"Polidocanol was found to be a more effective sclerosing agent than tetracycline for pleurodesis. "( The efficacy of polidocanol in pleurodesis in rats.
Akay, MT; Atalay, C; Cetin, A; Cetin, B; Koçkaya, EA, 2003
)
2.11
"Polidocanol is a synthetic, long-chain fatty acid that is widely used as a sclerosing agent in Europe."( Transcervical polidocanol as a nonsurgical method of female sterilization: a pilot study.
Jensen, JT; Liechtenstein-Zábrák, J; Rodriguez, MI; Zalanyi, S, 2004
)
1.41
"Polidocanol is an effective sclerosing agent that consists of 95% hydroxypolyethoxydodecane and 5% ethyl alcohol and is known to have a low risk of complications. "( Hepatotoxic effects of polidocanol in a model of autologously perfused porcine livers.
Dinh, QT; Groneberg, DA; Grosse-Siestrup, C; Nagel, S; Pfeffer, J; Springer, J; Unger, V; Witt, C; Wussow, A, 2004
)
2.08
"Polidocanol is an effective sclerosant that has few complications."( The Australian polidocanol (aethoxysklerol) study. Results at 2 years.
Conrad, P; Malouf, GM; Stacey, MC, 1995
)
2.09
"Polidocanol is a sclerosing solution that is highly valued by clinicians and patients for its painlessness, high efficacy, excellent safety profile, low incidence of side effects, and for the rarity of its allergic reactions. "( Allergic reactions to polidocanol for vein sclerosis. Two case reports.
Bond, OB; Bren, TS; Feied, CF; Fernando, CE; Hashemiyoon, RB; Jackson, JJ; Young, VC, 1994
)
2.05
"Polidocanol is a widely used sclerosing agent that was first developed as a local anesthetic. "( Indications for the sclerosing agent polidocanol (aetoxisclerol dexo, aethoxisklerol kreussler)
Guex, JJ, 1993
)
2
"Polidocanol sclerotherapy is a well-established therapeutic modality for the treatment of venous malformations. "( Reversible cardiac arrest after polidocanol sclerotherapy of peripheral venous malformation.
Abeni, D; Guerrini, P; Marrocco-Trischitta, MM; Stillo, F, 2002
)
2.04

Effects

Polidocanol has shown efficacy in the treatment of mucocele of minor salivary gland, hemangioma, upper extremity veins, reticular veins of the chest, facial veins, pyogenic granuloma, lymphangiomas circumscriptum, digital mucous cyst. Local complications have been reported after treatment.

ExcerptReferenceRelevance
"Polidocanol has shown efficacy in the treatment of mucocele of minor salivary gland, hemangioma, upper extremity veins, reticular veins of the chest, facial veins, pyogenic granuloma, lymphangioma circumscriptum, digital mucous cyst, mixed skin ulcers, cutaneous focal mucinosis, seromas, glomuvenous malformations, acne cysts, lymphocele, and dissecting cellulitis. "( Polidocanol: A Review of Off-Label Dermatologic Uses.
Bur, D; Nguyen, QD; Silapunt, S; Stender, C, 2022
)
3.61
"Polidocanol injections have been used to treat chronic Achilles tendinopathy in clinical settings, but the few studies published show inconsistent results. "( No beneficial effect of Polidocanol treatment in Achilles tendinopathy: a randomised controlled trial.
Ebbesen, BH; Gregersen, HE; Mølgaard, CM; Olesen, JL; Simonsen, O, 2018
)
2.23
"Polidocanol sclerotherapy has recently been reported to have excellent results and promises to replace operative treatments, but its efficacy in the case of aggressive aneurysmal bone cysts has not been documented."( Treatment of an aggressive aneurysmal bone cyst with percutaneous injection of polidocanol: a case report.
Brosjö, O; Tsagozis, P, 2014
)
1.35
"Polidocanol sclerotherapy has been reported as a potential treatment."( Treatment of 63 Subjects With Digital Mucous Cysts With Percutaneous Sclerotherapy Using Polidocanol.
Esson, GA; Holme, SA, 2016
)
1.38
"Polidocanol, which has been used for decades as an antipruritic and analgesic in various topical preparations at concentrations between 3% and 5%, might therefore be suitable for prophylaxis of recurrent pityriasis versicolor or in veterinary medicine."( Growth inhibition of Malassezia species by pharmacological concentrations of polidocanol.
Gründer, K; Mayser, P,
)
1.08
"Polidocanol has been widely used but local complications have been reported after treatment."( Endoscopic injection sclerotherapy in non-variceal upper gastrointestinal bleeding. A comparative study of polidocanol and thrombin.
Benedetti, G; Lacchin, T; Sablich, R, 1991
)
1.22

Treatment

Treatment with polidocanol endovenous microfoam 1% led to durable, clinically meaningful, and ongoing improvements at 1 year in varicose vein symptoms and appearance.

ExcerptReferenceRelevance
"Polidocanol as the sole treatment for a superficial orbital venous malformation in a horse was well tolerated and led to clinical resolution. "( Polidocanol monotherapy for a superficial orbital venous malformation in a horse.
Andres, M; Gilger, BC; Oh, A; Stonex, TM; Zibura, AE, 2022
)
3.61
"Treatment with polidocanol endovenous microfoam was associated with mild or moderate manageable side effects."( The VANISH-2 study: a randomized, blinded, multicenter study to evaluate the efficacy and safety of polidocanol endovenous microfoam 0.5% and 1.0% compared with placebo for the treatment of saphenofemoral junction incompetence.
Todd, KL; Wright, DI, 2014
)
0.96
"Treatment with polidocanol endovenous microfoam 1% led to durable, clinically meaningful, and ongoing improvements at 1 year in varicose vein symptoms and appearance. "( Durability of treatment effect with polidocanol endovenous microfoam on varicose vein symptoms and appearance (VANISH-2).
Todd, KL; Wright, DI, 2015
)
1.04

Toxicity

Eighty subjects were treated with either 1 or 3% polidocanol foam to compare the efficacy and adverse sequelae of each concentration. Ethanol treatment showed significantly more adverse reactions than polidOCanol and combination therapy.

ExcerptReferenceRelevance
" According to our actual experience and knowledge, the safe amount of foam should not exceed the 3-ml limit, but further advancements could come from standardization of the foam preparation technique."( Sclerosing foam in the treatment of varicose veins and telangiectases: history and analysis of safety and complications.
Cavezzi, A; Frullini, A, 2002
)
0.31
"Outpatient management is safe for patients with non-variceal upper-GI bleeding who are at low risk of recurrent bleeding and death."( A randomized study of the safety of outpatient care for patients with bleeding peptic ulcer treated by endoscopic injection.
Brullet, E; Cabrol, J; Calvet, X; Campo, R; Garcia-Monforte, N; Guell, M, 2004
)
0.32
"Eighty subjects were treated with either 1 or 3% polidocanol foam to compare the efficacy and adverse sequelae of each concentration of polidocanol foam."( Outcomes and side effects of duplex-guided sclerotherapy in the treatment of great saphenous veins with 1% versus 3% polidocanol foam: results of a randomized controlled trial with 1-year follow-up.
Bullens-Goessens, YI; Ceulen, RP; Nelemans, PJ; Pi-VAN DE Venne, SJ; Sommer, A; Veraart, JC, 2007
)
0.8
" No difference in adverse drug reactions was observed between treatment groups."( Efficacy and safety of great saphenous vein sclerotherapy using standardised polidocanol foam (ESAF): a randomised controlled multicentre clinical trial.
Otto, J; Pannier, F; Rabe, E; Schliephake, D, 2008
)
0.57
"Standardised 3% polidocanol foam is more efficient and equally safe compared to 3% liquid polidocanol for treatment of GSV."( Efficacy and safety of great saphenous vein sclerotherapy using standardised polidocanol foam (ESAF): a randomised controlled multicentre clinical trial.
Otto, J; Pannier, F; Rabe, E; Schliephake, D, 2008
)
0.92
"This clinical study evaluated prospectively adverse events immediately following ultrasound-guided foam sclerotherapy (UGFS) for the treatment of lower extremity venous valvular insufficiency."( Comparisons of side effects using air and carbon dioxide foam for endovenous chemical ablation.
Johnson, E; McEown, J; Morrison, N; Morrison, T; Neuhardt, DL; Rogers, CR; Salles-Cunha, SX, 2008
)
0.35
"Vital signs were monitored during and immediately after UGFS, and adverse events were recorded for 24 hours following the procedure."( Comparisons of side effects using air and carbon dioxide foam for endovenous chemical ablation.
Johnson, E; McEown, J; Morrison, N; Morrison, T; Neuhardt, DL; Rogers, CR; Salles-Cunha, SX, 2008
)
0.35
" Systemic adverse effects are rare."( [Polidocanol induced cardiotoxicity: a case report and review of the literature].
Blaise, S; Mallaret, M; Seinturier, C; Sylvoz, N; Villier, C, 2008
)
1.26
"Clinicians should be aware of the possibility of little-known but potentially serious cardiac adverse reaction with polidacanol injection and be prepared to initiate cardiopulmonary resuscitation if needed."( [Polidocanol induced cardiotoxicity: a case report and review of the literature].
Blaise, S; Mallaret, M; Seinturier, C; Sylvoz, N; Villier, C, 2008
)
1.26
" Adverse events included hypotension and bradycardia during the procedure."( Polidocanol sclerotherapy for painful venous malformations: evaluation of safety and efficacy in pain relief.
Fujiwara, H; Gobara, H; Hiraki, T; Hyodo, T; Iguchi, T; Kanazawa, S; Kimata, Y; Mimura, H; Mukai, T; Yasui, K, 2009
)
1.8
" Although foam-induced microembolism is a common phenomenon during sclerotherapy, in this report we demonstrate that polidocanol microfoam prepared with a low-nitrogen gas mixture is safe in a patient with a patent foramen ovale."( Efficacy and safety of microfoam sclerotherapy in a patient with Klippel-Trenaunay syndrome and a patent foramen ovale.
Bastarrika, G; Cabrera, J; Martínez-Cuesta, A; Redondo, P; Sierra, A, 2009
)
0.56
" The objective of this follow-up registry was to evaluate the long-term incidence of adverse events with polidocanol."( The French polidocanol study on long-term side effects: a survey covering 3,357 patient years.
Allaert, FA; Guex, JJ; Mako, S; Otto, J; Schliephake, DE, 2010
)
0.96
"4%) adverse events were observed in patients treated with liquid polidocanol and 46 (1."( The French polidocanol study on long-term side effects: a survey covering 3,357 patient years.
Allaert, FA; Guex, JJ; Mako, S; Otto, J; Schliephake, DE, 2010
)
0.99
" This study demonstrates that polidocanol is a safe sclerosing agent in the short and long term."( The French polidocanol study on long-term side effects: a survey covering 3,357 patient years.
Allaert, FA; Guex, JJ; Mako, S; Otto, J; Schliephake, DE, 2010
)
1.04
" There were no major adverse events."( Endovenous mechanochemical ablation of great saphenous vein incompetence using the ClariVein device: a safety study.
Boersma, D; de Vries, JP; Elias, S; Holewijn, S; Reijnen, MM; van Eekeren, RR; Werson, DA, 2011
)
0.37
"This study showed that endovenous MOCA, using polidocanol, is feasible and safe in the treatment of GSV incompetence."( Endovenous mechanochemical ablation of great saphenous vein incompetence using the ClariVein device: a safety study.
Boersma, D; de Vries, JP; Elias, S; Holewijn, S; Reijnen, MM; van Eekeren, RR; Werson, DA, 2011
)
0.63
"5%, 1% and 3% was efficacious and safe in Chinese patients."( Efficacy and safety of Aethoxysklerol® (polidocanol) 0.5%, 1% and 3% in comparison with placebo solution for the treatment of varicose veins of the lower extremities in Chinese patients (ESA-China Study).
Gu, YQ; Jing, Z; Malouf, GM; Otto, J; Schliephake, DE; Zhang, J, 2012
)
0.65
" Sodium lauryl ether sulfate and polyoxyethylene lauryl ether significantly damaged the membrane, disturbed cellular metabolic activity, and decreased mitochondrial activity and the protein synthesis rate; however, their toxicity was far below those of the severely toxic chemicals at comparable concentrations."( Cellular toxicity of surfactants used as herbicide additives.
Gil, HW; Hong, SY; Kim, YH; Lee, EY; Seok, SJ; Song, HY; Yang, JO, 2012
)
0.38
" In addition, major adverse effects were rare."( Efficacy and safety of endovenous foam sclerotherapy: meta-analysis for treatment of venous disorders.
Norris, A; Rathbun, S; Stoner, J, 2012
)
0.38
"EFS is a safe and effective therapy for the treatment of venous disorders."( Efficacy and safety of endovenous foam sclerotherapy: meta-analysis for treatment of venous disorders.
Norris, A; Rathbun, S; Stoner, J, 2012
)
0.38
" Efficacy of combining POL and laser proved safe and satisfactory in 96 % of patients using low-fluence laser pulses with a total cumulative energy in the 3 cm venous segment, lower than that of conventional treatment."( Optimal and safe treatment of spider leg veins measuring less than 1.5 mm on skin type IV patients, using repeated low-fluence Nd:YAG laser pulses after polidocanol injection.
Alcolea, J; Hernández, E; Isarría, MJ; Moreno-Moraga, J; Pascu, ML; Royo, J; Smarandache, A; Trelles, M, 2013
)
0.59
"In the therapy of first-grade haemorrhoidal disease, polidocanol 3 % foam is more effective and equally safe compared to liquid polidocanol."( Efficacy and safety of sclerotherapy with polidocanol foam in comparison with fluid sclerosant in the treatment of first-grade haemorrhoidal disease: a randomised, controlled, single-blind, multicentre trial.
Bussen, DG; Gliem, P; Joos, AK; Kirsch, J; Mosch, C; Moser, KH; Sauerland, S; Walgenbach, M, 2013
)
0.9
" Of the 230 polidocanol endovenous microfoam-treated patients (including open-label patients), 60% had an adverse event compared with 39% of placebo; 95% were mild or moderate."( The VANISH-2 study: a randomized, blinded, multicenter study to evaluate the efficacy and safety of polidocanol endovenous microfoam 0.5% and 1.0% compared with placebo for the treatment of saphenofemoral junction incompetence.
Todd, KL; Wright, DI, 2014
)
1
" Adverse events included contusion, incision-site hematoma, and limb discomfort."( A multicenter, randomized, placebo-controlled study to evaluate the efficacy and safety of Varithena® (polidocanol endovenous microfoam 1%) for symptomatic, visible varicose veins with saphenofemoral junction incompetence.
Gibson, K; Kabnick, L, 2017
)
0.67
"Polidocanol foam sclerotherapy is effective, and safe for treatment of VMs, with high success rate and low risk of major complications."( Efficacy and safety of Duplex-guided polidocanol foam sclerotherapy for venous malformations.
Ali, H; Mohammed, W; Saleh, M, 2017
)
2.17
"EUS-guided PCN ablation with lauromacrogol is safe and efficient."( A prospective study on the safety and effectiveness of using lauromacrogol for ablation of pancreatic cystic neoplasms with the aid of EUS.
Chai, N; Du, C; Feng, J; Guo, X; Li, H; Linghu, E; Ning, B; Sun, L; Sun, Y; Tang, P; Wang, X; Wang, Z; Xu, W; Zhang, W, 2017
)
0.46
" A meta-analysis on the risk of adverse events (AEs) showed a lower risk for polidocanol versus other treatments, for example, all the conventional treatments used independently (p < ."( Effectiveness and safety of polidocanol for the treatment of hemangiomas and vascular malformations: A meta-analysis.
Gao, Z; Li, W; Shi, C; Zhang, Y, 2018
)
1
"BRTO utilizing lauromacrogol foam appears to be a safe and useful treatment option in patients with GVs in the short term."( Efficacy and safety of balloon-occluded retrograde transvenous obliteration of gastric varices with lauromacrogol foam sclerotherapy: initial experience.
Luo, X; Ma, H; Wang, X; Yang, L; Yu, J; Zhao, Y, 2018
)
0.48
"The authors performed a disproportionality analysis using the proportional reporting ratio (PRR) method to compare pharmacovigilance signals between each sclerosing agent among 6 adverse event syndromes of interest: hypersensitivity reactions, arterial thromboembolic disorders, venous thromboembolic disorders, cardiac arrhythmias, visual/neurological disturbances, and skin ulcerations."( Safety Profile of Sclerosing Agents: An Analysis From the World Health Organization Pharmacovigilance Database VigiBase.
Blaise, S; Cracowski, JL; Khouri, C; Roselli, A; Roustit, M, 2019
)
0.51
"The efficacy of lauromacrogol injection therapy and intralesional triamcinolone for infantile hemangiomas (IH) has been well documented recently, but with an increase in serious or rare adverse reactions."( Safety of intralesional injection of lauromacrogol combined with triamcinolone for infantile hemangiomas.
Bi, J; Chai, Y; Huo, R; Li, X; Li, Z; Lv, R; Song, J; Xu, G; Zhou, Z, 2019
)
0.51
"The sequential treatment regimen, including percutaneous polidocanol sclerotherapy and RFA, is an appropriate and safe treatment strategy for large benign partially cystic thyroid nodules with solid components."( Sequential treatment by polidocanol and radiofrequency ablation of large benign partially cystic thyroid nodules with solid components: Efficacy and safety.
Ding, M; He, Y; Li, P; Lin, Y; Shi, YP; Tang, XY; Zhai, B, 2020
)
1.11
"Percutaneous sclerotherapy is a safe and effective treatment option of VM and secondary varicosis of the labia majora."( Safety and effectiveness of percutaneous sclerotherapy for venous disorders of the labia majora in patients with vascular malformations.
Brill, R; Deistung, A; Goldann, C; Gussew, A; Rosendahl, J; Stangl, F; Uller, W; Wildgruber, M; Wohlgemuth, WA, 2020
)
0.56
" No patients experienced adverse hemodynamic consequences or venous thromboembolism."( Safety and efficacy of foam sclerotherapy for treatment of low-flow vascular malformations in children.
Markovic, JN; Nag, U; Shortell, CK, 2020
)
0.56
"DSA-guided percutaneous sclerotherapy for venous malformations of penile region in children is safe and effective, does not affect the appearance and function of penis, and is worthy of clinical promotion."( Efficacy and safety of DSA-guided percutaneous sclerotherapy for venous malformations of penile region in children.
Guo, L; Li, J; Song, D; Wang, L; Wu, C; Zhang, X, 2021
)
0.62
" Adverse events (AEs) and efficacy were evaluated by both subject and blinded investigator."( Comparison of the Safety and Efficacy of Foam Sclerotherapy With 1: 2 Polidocanol to Air Ratio Versus 1: 4 Ratio for the Treatment of Reticular Veins of the Lower Extremities.
Alhaddad, M; Boen, M; Goldman, MP; Hoss, E; Kollipara, R, 2020
)
0.79
"Two different POL to air ratios, 1:2 versus 1:4, were similarly safe and efficacious for the treatment reticular veins of the lower extremities."( Comparison of the Safety and Efficacy of Foam Sclerotherapy With 1: 2 Polidocanol to Air Ratio Versus 1: 4 Ratio for the Treatment of Reticular Veins of the Lower Extremities.
Alhaddad, M; Boen, M; Goldman, MP; Hoss, E; Kollipara, R, 2020
)
0.79
"Sclerosis with foam and liquid polidocanol were superior to the other groups, but specially polidocanol foam at the expense of greater frequency of adverse events."( Efficacy and safety of glucose, glucose and polidocanol combination, liquid polidocanol and polidocanol foam in the treatment of reticular veins: A randomized study in rabbits.
Bertanha, M; Carvalho, LR; Jaldin, RG; Janzen, J; Lucio Filho, CEP; Prata, MP; Sobreira, ML; Yoshida, WB, 2021
)
1.17
" Ethanol treatment showed significantly more adverse reactions than polidocanol and combination therapy."( Effectiveness and Safety of Ethanol for the Treatment of Venous Malformations: A Meta-Analysis.
Chen, X; Guo, Y; Lei, S; Sun, Y, 2020
)
0.79
"Absolute ethanol combined with polidocanol is more effective in treating VM and has fewer adverse reactions."( Effectiveness and Safety of Ethanol for the Treatment of Venous Malformations: A Meta-Analysis.
Chen, X; Guo, Y; Lei, S; Sun, Y, 2020
)
0.84
"TLFS combined with EVLA is a safe and feasible procedure that improves the VCSS and reduces the need for additional second-stage interventions compared with UGFS combined with EVLA."( A randomized controlled trial to evaluate the safety and efficacy of transluminal injection of foam sclerotherapy compared with ultrasound-guided foam sclerotherapy during endovenous catheter ablation in patients with varicose veins.
Fujii, K; Iwakura, K; Iwamoto, M; Nagai, H; Okamura, A; Sumiyoshi, A; Suzuki, S; Tanaka, H; Tanaka, K; Watanabe, S, 2022
)
0.72
" The demographic data, CEAP (clinical, etiologic, anatomic, pathophysiologic) classification, venous clinical severity score (VCSS), procedure details, adverse thrombotic events, and follow-up data were abstracted."( Endovenous microfoam ablation of below knee superficial truncal veins is safe and effective in patients with prior saphenous treatment across a wide range of CEAP classes.
DeRubertis, BG; Farley, SM; Jimenez, JC; Lawrence, PF; Pavlyha, M; Rigberg, DA; Woo, K, 2022
)
0.72
" No pulmonary emboli or neurologic adverse events were reported."( Endovenous microfoam ablation of below knee superficial truncal veins is safe and effective in patients with prior saphenous treatment across a wide range of CEAP classes.
DeRubertis, BG; Farley, SM; Jimenez, JC; Lawrence, PF; Pavlyha, M; Rigberg, DA; Woo, K, 2022
)
0.72
"Endovenous chemical ablation with commercially manufactured polidocanol microfoam of BK truncal veins is a safe and effective treatment for patients with severe, refractory chronic venous insufficiency and prior saphenous interventions."( Endovenous microfoam ablation of below knee superficial truncal veins is safe and effective in patients with prior saphenous treatment across a wide range of CEAP classes.
DeRubertis, BG; Farley, SM; Jimenez, JC; Lawrence, PF; Pavlyha, M; Rigberg, DA; Woo, K, 2022
)
0.96
" No serious adverse events occurred."( A multicentre, open-label, single-arm phase II trial of the efficacy and safety of sclerotherapy using 3% polidocanol foam to treat second-degree haemorrhoids (SCLEROFOAM).
Bianco, V; Diaco, E; Gallo, G; Giuliani, A; Laforgia, R; Lobascio, P; Luc, AR; Moggia, E; Naldini, G; Novelli, E; Perinotti, R; Pietroletti, R; Pozzo, M; Roveroni, M; Sammarco, G; Sturiale, A; Trompetto, M; Tutino, R, 2022
)
0.93
"To analyze adverse events (AEs) related to sclerosants reported through the Federal Adverse Event Reporting System (FAERS)."( Analysis of adverse events with sclerosants reported to the United States Food and Drug Administration.
Nguyen, CN; Nguyen, QD; Silapunt, S, 2022
)
0.72
"Percutaneous sclerotherapy can be effective and safe for maxillofacial intramuscular venous malformations, especially for localized lesions of the masseter muscle."( Effectiveness and safety of percutaneous sclerotherapy using absolute ethanol and/or polidocanol for maxillofacial venous malformations involving the masticatory muscles: A case series.
Funayama, E; Furukawa, H; Ishikawa, K; Maeda, T; Miura, T; Sasaki, S; Sasaki, Y; Yamamoto, Y, 2023
)
1.13
"To assess the effectiveness, safety, and predictors of outcomes and adverse events for percutaneous sclerotherapy using polidocanol for the treatment of venous malformations (VMs)."( Sclerotherapy of Venous Malformations Using Polidocanol: Effectiveness, Safety, and Predictors of Outcomes and Adverse Events.
Bendszus, M; Günther, P; Hoffmann, J; Hohenstatt, S; Lorenz, J; Möhlenbruch, MA; Ruping, F; Schmitt, N; Semmelmayer, K; Vollherbst, DF, 2023
)
1.38
" Demographic characteristics, clinical data, and radiologic features were analyzed, and the influence of patient- and VM-related factors on the subjective clinical outcome and adverse events were investigated using a multivariate logistic regression analysis."( Sclerotherapy of Venous Malformations Using Polidocanol: Effectiveness, Safety, and Predictors of Outcomes and Adverse Events.
Bendszus, M; Günther, P; Hoffmann, J; Hohenstatt, S; Lorenz, J; Möhlenbruch, MA; Ruping, F; Schmitt, N; Semmelmayer, K; Vollherbst, DF, 2023
)
1.17
" The total adverse event rate was 10."( Sclerotherapy of Venous Malformations Using Polidocanol: Effectiveness, Safety, and Predictors of Outcomes and Adverse Events.
Bendszus, M; Günther, P; Hoffmann, J; Hohenstatt, S; Lorenz, J; Möhlenbruch, MA; Ruping, F; Schmitt, N; Semmelmayer, K; Vollherbst, DF, 2023
)
1.17
" However, it can be less effective in children, and adverse events can be more frequently expected for VMs of the extremities."( Sclerotherapy of Venous Malformations Using Polidocanol: Effectiveness, Safety, and Predictors of Outcomes and Adverse Events.
Bendszus, M; Günther, P; Hoffmann, J; Hohenstatt, S; Lorenz, J; Möhlenbruch, MA; Ruping, F; Schmitt, N; Semmelmayer, K; Vollherbst, DF, 2023
)
1.17

Compound-Compound Interactions

Polidocanol sclerotherapy combined with transarterial embolization using NBCA is safe and effective for treating extracranial AVMs with an acceptable risk of minor complications.

ExcerptReferenceRelevance
"A randomized comparative study was conducted of injection therapy with epinephrine-polidocanol (1%) versus hemoclip application, versus injection combined with hemoclip for bleeding peptic ulcers."( A randomized trial comparing injection therapy with hemoclip and with injection combined with hemoclip for bleeding ulcers.
De Goede, E; Gevers, AM; Hiele, M; Rutgeerts, P; Simoens, M, 2002
)
0.54
" We describe in detail a patient who received treatment with ultrasound-guided laser interruption of feeding vessels combined with polidocanol sclerotherapy after the recurrence of forearm high-flow vascular malformation."( High-flow vascular malformation treatment using ultrasound-guided laser combined with polidocanol sclerotherapy.
Li, JL; Li, L; Zhang, Y; Zhou, P, 2015
)
0.84
" This result indicates that soil washing combined with Fenton-like oxidation may be a practical approach for the remediation of PCB-contaminated soil."( Soil washing in combination with homogeneous Fenton-like oxidation for the removal of 2,4,4'-trichlorodiphenyl from soil contaminated with capacitor oil.
Dong, YH; Lin, ZR; Ma, XH; Zhao, L, 2016
)
0.43
"To evaluate the effect of ultrasound-guided foam sclerotherapy (UGFS) in a single session combined with great saphenous vein (GSV) high ligation for severe lower extremity varicosis classified as C4-C6, compared with GSV stripping plus multistab avulsion or transilluminated powered phlebectomy (TIPP)."( Prospective Randomized Study of Ultrasound-Guided Foam Sclerotherapy Combined with Great Saphenous Vein High Ligation in the Treatment of Severe Lower Extremity Varicosis.
Chang, G; He, H; Hu, Z; Li, Z; Wang, J; Wang, M; Wang, S; Yao, C; Yin, H, 2017
)
0.46
" The UGFS group was managed by GSV high ligation and foam sclerotherapy in one session under the surveillance of ultrasonography, whereas the control group received GSV high ligation and stripping combined with multistab avulsion or TIPP."( Prospective Randomized Study of Ultrasound-Guided Foam Sclerotherapy Combined with Great Saphenous Vein High Ligation in the Treatment of Severe Lower Extremity Varicosis.
Chang, G; He, H; Hu, Z; Li, Z; Wang, J; Wang, M; Wang, S; Yao, C; Yin, H, 2017
)
0.46
"Our outcomes indicated that UGFS combined with GSV high ligation was safe and effective for severe lower extremity varicosis."( Prospective Randomized Study of Ultrasound-Guided Foam Sclerotherapy Combined with Great Saphenous Vein High Ligation in the Treatment of Severe Lower Extremity Varicosis.
Chang, G; He, H; Hu, Z; Li, Z; Wang, J; Wang, M; Wang, S; Yao, C; Yin, H, 2017
)
0.46
"To compare the clinical efficacy of pingyangmycin and lauromacrogol combined with pingyangmycin in the treatment of venous malformations (VMs)."( [Clinical efficacy of lauromacrogol combined with pingyangmycin in the treatment of venous malformation: clinical analysis of 120 consecutive cases].
Cai, Y; Liu, DX; Liu, L; Zhao, JH; Zhong, HY, 2016
)
0.43
"One hundred and twenty patients with VM were randomly divided into lauromacrogol combined with pingyangmycin injection group (experimental group) and pingyangmycin injection group (control group)."( [Clinical efficacy of lauromacrogol combined with pingyangmycin in the treatment of venous malformation: clinical analysis of 120 consecutive cases].
Cai, Y; Liu, DX; Liu, L; Zhao, JH; Zhong, HY, 2016
)
0.43
"Compared to the single use of pingyangmycin, lauromacrogol combined with pingyangmycin is more effective for the treatment of VM, with fewer sessions required and no adverse effects."( [Clinical efficacy of lauromacrogol combined with pingyangmycin in the treatment of venous malformation: clinical analysis of 120 consecutive cases].
Cai, Y; Liu, DX; Liu, L; Zhao, JH; Zhong, HY, 2016
)
0.43
"The purpose of this prospective study was to evaluate the occlusion rate, clinical severity, disease specific health related quality of life (HRQoL), and safety in patients with great saphenous vein (GSV) reflux 3 years after a single treatment session of catheter directed foam sclerotherapy (CDFS) combined with peri-saphenous infiltration of tumescent local anaesthesia (TLA)."( Mid-term Results of Catheter Directed Foam Sclerotherapy Combined with Tumescent Local Anaesthesia for Treatment of Great Saphenous Vein Incompetence.
Ali, H; Elbadawy, A; Mahmoud, O; Saleh, M, 2017
)
0.46
"A total of 249 patients with symptomatic unilateral GSV incompetence underwent CDFS combined with TLA and were followed up for 3 years."( Mid-term Results of Catheter Directed Foam Sclerotherapy Combined with Tumescent Local Anaesthesia for Treatment of Great Saphenous Vein Incompetence.
Ali, H; Elbadawy, A; Mahmoud, O; Saleh, M, 2017
)
0.46
"CDFS combined with TLA for treatment of GSV incompetence yields good mid-term results in terms of occlusion rate, clinical severity, patients' QoL, and safety."( Mid-term Results of Catheter Directed Foam Sclerotherapy Combined with Tumescent Local Anaesthesia for Treatment of Great Saphenous Vein Incompetence.
Ali, H; Elbadawy, A; Mahmoud, O; Saleh, M, 2017
)
0.46
" In this case report, EUS-guided radiofrequency ablation combined with lauromacrogol ablation was applied for the first time in the treatment of PCN, and it showed complete resolution at a 3-month follow-up."( New treatment of the pancreatic cystic neoplasm: Endoscopic ultrasonography-guided radiofrequency ablation combined with lauromacrogol ablation.
Chai, N; Feng, X; Li, H; Linghu, E, 2018
)
0.48
"To evaluate the efficacy of ultrasound-guided local lauromacrogol injection combined with aspiration for treating cesarean scar pregnancy (CSP)."( Evaluation of the Efficacy of Ultrasound-Guided Local Lauromacrogol Injection Combined with Aspiration for Cesarean Scar Pregnancy: A Novel Treatment.
Chai, ZY; Liu, MM; Qi, F; Yu, L; Zhu, TW, 2018
)
0.48
"From July 2016 to December 2016, 18 patients diagnosed with CSP were treated with ultrasound-guided local lauromacrogol injection combined with aspiration."( Evaluation of the Efficacy of Ultrasound-Guided Local Lauromacrogol Injection Combined with Aspiration for Cesarean Scar Pregnancy: A Novel Treatment.
Chai, ZY; Liu, MM; Qi, F; Yu, L; Zhu, TW, 2018
)
0.48
"Ultrasound-guided local lauromacrogol injection combined with aspiration is an effective CSP therapy, as it was associated with a high success rate, short hospitalization and fast recovery."( Evaluation of the Efficacy of Ultrasound-Guided Local Lauromacrogol Injection Combined with Aspiration for Cesarean Scar Pregnancy: A Novel Treatment.
Chai, ZY; Liu, MM; Qi, F; Yu, L; Zhu, TW, 2018
)
0.48
"To assess the safety and effectiveness of polidocanol sclerotherapy combined with transarterial embolization using a liquid adhesive agent (n-butyl cyanoacrylate, NBCA) for treatment of extracranial arteriovenous malformations (AVMs)."( Polidocanol Sclerotherapy Combined with Transarterial Embolization Using n-Butyl Cyanoacrylate for Extracranial Arteriovenous Malformations.
Hagihara, M; Ikeda, S; Ishiguchi, T; Izumi, Y; Kitagawa, A; Matsunaga, N; Ota, T; Yamaji, M; Yamamoto, T, 2018
)
2.19
"Polidocanol sclerotherapy combined with transarterial embolization using NBCA is safe and effective for treating extracranial AVMs with an acceptable risk of minor complications."( Polidocanol Sclerotherapy Combined with Transarterial Embolization Using n-Butyl Cyanoacrylate for Extracranial Arteriovenous Malformations.
Hagihara, M; Ikeda, S; Ishiguchi, T; Izumi, Y; Kitagawa, A; Matsunaga, N; Ota, T; Yamaji, M; Yamamoto, T, 2018
)
3.37
"To investigate the clinical effect of radiofrequency ablation (RFA) combined with lauromacrogol for the treatment of parotid gland hemangioma in infants."( [Clinical study of radiofrequency ablation combined with lauromacrogol for the treatment of parotid gland hemangioma in infants].
Chen, H; Chen, J; Cui, J; Han, T; Ji, Y; Shen, W; Zou, J, 2016
)
0.43
"The observation group was treated by RFA combined with lauromacrogol, while the control group 1 was treated by RFA only, the control group 2 was treated by pingyangmycin only, and the control group 3 received additional pingyangmycin based on RFA."( [Clinical study of radiofrequency ablation combined with lauromacrogol for the treatment of parotid gland hemangioma in infants].
Chen, H; Chen, J; Cui, J; Han, T; Ji, Y; Shen, W; Zou, J, 2016
)
0.43
" The aim of this study is to investigate the safety concerns regarding intralesional injection of lauromacrogol combined with triamcinolone for IH and to study its effect on infant growth and development."( Safety of intralesional injection of lauromacrogol combined with triamcinolone for infantile hemangiomas.
Bi, J; Chai, Y; Huo, R; Li, X; Li, Z; Lv, R; Song, J; Xu, G; Zhou, Z, 2019
)
0.51
"Ultrasound-guided local lauromacrogol injection combined with suction curettage may be a safer and novel therapeutic method."( Type II caesarean scar pregnancy management by ultrasound-guided local lauromacrogol injection in combination with suction curettage: A case report.
Jia, CL; Li, DH; Sun, WC; Wei, SS; Zhang, ZF, 2020
)
0.56
"To investigate the clinical efficacy and safety of bipolar coagulation forceps combined with 1% lauromacrogol foam sclerotherapy in the treatment of microcystic lymphatic malformation of tongue."( [Evaluation of the effectiveness of treatment of 16 patients with tongue microcystic lymphatic malformation using bipolar coagulation forceps combined with 1% lauromacrogol foam sclerotherapy].
Chen, JF; He, XM; Li, J; Li, JP; Liu, SW; Xian, D; Zhang, GR, 2021
)
0.62
"Bipolar coagulation forceps combined with 1% lauromacrogol foam sclerotherapy is a minimally invasive, safe and effective treatment for tongue microcystic lymphatic malformation."( [Evaluation of the effectiveness of treatment of 16 patients with tongue microcystic lymphatic malformation using bipolar coagulation forceps combined with 1% lauromacrogol foam sclerotherapy].
Chen, JF; He, XM; Li, J; Li, JP; Liu, SW; Xian, D; Zhang, GR, 2021
)
0.62
", cryoablation and microwave ablation) in combination with sclerotherapy using lauromacrogol."( Sequential thermal ablation in combination with sclerotherapy using lauromacrogol as a successful translative therapy for an unresectable huge biliary cystadenocarcinoma: The first experience assisted by contrast-enhanced ultrasound.
Li, JX; Li, XL; Sun, LP; Xu, HX; Yu, SY; Zhang, HL; Zhu, JE, 2022
)
0.72
"To explore factors related to local injection of Lauromacrogol combined with curettage in the treatment of cesarean scar pregnancy."( Predictive factors analysis of cesarean scar pregnancy treated by local injection of Lauromacrogol combined with curettage.
He, P; Huang, J; Li, D; Zhou, J, 2023
)
0.91

Bioavailability

ExcerptReferenceRelevance
" The presence of sodium salicylate and a nonionic surface-active agent, Brij 35, gave increased bioavailability as high as 20% compared with 3% for a system without adjuvants."( Use of adjuvants for enhancement of rectal absorption of cefoxitin in humans.
Burnham, WR; Davis, SS; O'Brien, J; Wilson, P, 1985
)
0.27
" The degree of inhibition of oedema development was quite similar after oral and intravenous administration, respectively, thus the bioavailability of clobenoside should be good."( [Edema-protective effect of clobenoside].
Felix, W; Hennings, G; Ruppert, R, 1985
)
0.27
"The principal objective of this study was to quantify the bioavailability of micelle-solubilized naphthalene to naphthalene-degrading microorganisms comprising a mixed population isolated from contaminated waste and soils."( Biodegradation of naphthalene in aqueous nonionic surfactant systems.
Jacobson, AM; Liu, Z; Luthy, RG, 1995
)
0.29
"The need to develop chloroquine suppository formulations that yield optimal bioavailability of the drug has been emphasized."( Effects of absorption enhancers in chloroquine suppository formulations: I. In vitro release characteristics.
Adebayo, AS; Babalola, CP; Onyeji, CO, 1999
)
0.3
"Pulmonary drug administration of most peptide/protein drugs is characterized by low bioavailability due to low permeability."( Histopathological study of the effects of a single intratracheal instillation of surface active agents on lung in rats.
Adachi, K; Awazu, S; Hayashi, M; Machida, M; Otabe, K; Sugimoto, T; Suzuki, M, 2000
)
0.31
"The effect of the nonionic surfactant Brij 35 on the bioavailability of solid and Teflon-sorbed dibenzofuran for Sphingomonas sp."( Influence of the nonionic surfactant Brij 35 on the bioavailability of solid and sorbed dibenzofuran.
Garcia, JM; Harms, H; Wick, LY, 2001
)
0.31
" Overall, this study demonstrates that the properties of the surfactant and its dose relative to the corresponding aqueous-phase concentration are important factors in designing systems for surfactant-enhanced bioremediation of PAH-contaminated soils in which PAH bioavailability is limited."( Surfactant-enhanced desorption and biodegradation of polycyclic aromatic hydrocarbons in contaminated soil.
Aitken, MD; Zhu, H, 2010
)
0.36
"In the present study surfactant addition with the help of either a mechanical dispersion or a thermal treatment was applied in order to increase the solubility and the bioavailability of phenanthrene in aqueous media, and therefore to promote its biodegradation."( Effect of surfactants, dispersion and temperature on solubility and biodegradation of phenanthrene in aqueous media.
Blanchard, F; Boudrant, J; Delaunay, S; Goergen, JL; Guédon, E; Guseva, E; Pantsyrnaya, T, 2011
)
0.37
"High recalcitrant characteristics and low bioavailability rates due to aging processes can hinder high molecular weight polycyclic aromatic hydrocarbons (HMW-PAHs) bioremediation in real industrial polluted soils."( Comparative assessment of bioremediation approaches to highly recalcitrant PAH degradation in a real industrial polluted soil.
Covino, S; D'annibale, A; Lladó, S; Petruccioli, M; Solanas, AM; Viñas, M, 2013
)
0.39
"Recent studies have suggested that the ability of a surfactant to enhance the bioavailability of hydrophobic organic compounds (HOC) requires the formation of surfactant hemi-micelles on the bacterial cell surface and subsequent partitioning of HOC into the hemi-micelles."( Partitioning of phenanthrene into surfactant hemi-micelles on the bacterial cell surface and implications for surfactant-enhanced biodegradation.
Brown, DG; Lanzon, JB, 2013
)
0.39
" Furthermore, the TMNM had greater bioavailability (215%) than the Tol solution."( Toltrazuril mixed nanomicelle delivery system based on sodium deoxycholate-Brij C20 polyethylene ether-triton x100: Characterization, solubility, and bioavailability study.
Fan, G; Fu, H; Liu, C; Peng, G; Ren, D; Shi, F; Shu, G; Yin, L; Yuan, Z; Zhang, L; Zhao, L; Zhou, J, 2018
)
0.48
" The SD formulation was effective in improving the bioavailability of topotecan, a BCRP substrate in rats."( Improved In vivo Effect of Chrysin as an Absorption Enhancer Via the Preparation of Ternary Solid Dispersion with Brij®L4 and Aminoclay.
Han, HK; Lee, SH; Lee, YS; Song, JG, 2019
)
0.51
"The ATP-binding cassette transporter P-glycoprotein (P-gp) is known to limit both brain penetration and oral bioavailability of many chemotherapy drugs."( A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
Ambudkar, SV; Brimacombe, KR; Chen, L; Gottesman, MM; Guha, R; Hall, MD; Klumpp-Thomas, C; Lee, OW; Lee, TD; Lusvarghi, S; Robey, RW; Shen, M; Tebase, BG, 2019
)
0.51

Dosage Studied

This study was conducted to identify the ideal Polidocanol dosage and form for mechano-chemical ablation in order to occlude the great saphenous vein.

ExcerptRelevanceReference
" In addition, in vivo repeated dosing of RM beta-CD did not show any toxicity up to 20% w/v."( The effects of water-soluble cyclodextrins on the histological integrity of the rat nasal mucosa.
Asai, K; Hosoda, S; Katsuta, H; Morishita, M; Nagai, T; Noro, M; Shinomiya, K; Takayama, K, 2002
)
0.31
"Practice is variable, even in areas with established evidence based on randomized controlled studies, such as dosage and way of administration and duration of PPI treatment, injection treatment used as monotherapy and the volume used, including ulcers with clots for treatment, and the use of scheduled second-look endoscopy."( Clinical practice and evidence in endoscopic treatment of bleeding peptic gastroduodenal ulcer.
Adamsen, S; Bendix, J; Kallehave, F; Moesgaard, F; Nilsson, T; Wille-Jørgensen, P, 2007
)
0.34
" More research is needed to determine the optimal agent(s) and the ideal dosing to achieve the best results and maximize patient satisfaction."( Sclerotherapy for lower limb telangiectasias.
Maxwell, H; Schwartz, L, 2011
)
0.37
" All patients were able to perform sexual intercourse without the previously used dosage of PDE5 inhibitor."( Venous leakage treatment revisited: pelvic venoablation using aethoxysclerol under air block technique and Valsalva maneuver.
Herwig, R; Sansalone, S, 2015
)
0.42
" However, determining the precise dosage for satisfactory efficacy and few side effects are still challenging."( A new method for using radiopaque sclerosing foam to treat venous malformations.
Chen, AW; Li, K; Liu, SH; Liu, YR, 2015
)
0.42
" Increasing the TiO2 dosage exhibited a positive effect on treatment efficiencies."( A comparative study of HO•- and SO4•--based AOPs for the degradation of non-ionic surfactant Brij30.
Ecer, Ç; Kabdaşlı, I; Olmez-Hanci, T; Tünay, O, 2015
)
0.42
" This study was conducted to identify the ideal Polidocanol dosage and form for mechano-chemical ablation in order to occlude the great saphenous vein."( Clarivein® mechano-chemical ablation an interim analysis of a randomized controlled trial dose-finding study.
Lam, YL; Toonder, IM; Wittens, CH, 2016
)
0.69
" Further investigation to determine the ideal Polidocanol liquid dosage with mechano-chemical ablation is advocated and is being conducted accordingly."( Clarivein® mechano-chemical ablation an interim analysis of a randomized controlled trial dose-finding study.
Lam, YL; Toonder, IM; Wittens, CH, 2016
)
0.69
"000), whereas no difference was observed in the dosage of lauromacrogol (16."( Transparent cap-assisted endoscopic sclerotherapy in esophageal varices: a randomized-controlled trial.
Chen, S; Huang, X; Lian, J; Ma, L; Wang, J, 2018
)
0.48
" The mean difference for average tissue adhesive dosage per case was calculated."( Sandwich method with or without lauromacrogol in the treatment of gastric variceal bleeding with liver cirrhosis: A meta-analysis.
Gou, Y; He, S; Song, Q; Wu, K, 2019
)
0.51
"The OD values of HUVECs treated with HA first increased and then decreased with the growing dosage of HA while cells treated with HA-POL died."( The role of hyaluronic acid in polidocanol foam: An in vitro study.
Azmoun, S; Dongjian, L; Shaohua, L; Xuanxuan, S; Ziyi, L, 2022
)
1.01
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
nonionic surfactantA surfactant with an uncharged hydrophilic headgroup.
hepatotoxic agentA role played by a chemical compound exihibiting itself through the ability to induce damage to the liver in animals.
sclerotherapy agentA sclerotherapy agent is used to treat blood vessels or blood vessel malformations (vascular malformations) and also those of the lymphatic system by injection into the vessels, which makes them shrink.
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (1)

ClassDescription
hydroxypolyetherA hydroxyether compound containing more than one ether group.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Protein Targets (49)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
phosphopantetheinyl transferaseBacillus subtilisPotency70.79460.141337.9142100.0000AID1490
hypoxia-inducible factor 1 alpha subunitHomo sapiens (human)Potency26.83253.189029.884159.4836AID1224846
RAR-related orphan receptor gammaMus musculus (house mouse)Potency7.18420.006038.004119,952.5996AID1159521; AID1159523
SMAD family member 2Homo sapiens (human)Potency9.52050.173734.304761.8120AID1346924
USP1 protein, partialHomo sapiens (human)Potency56.23410.031637.5844354.8130AID504865
SMAD family member 3Homo sapiens (human)Potency9.52050.173734.304761.8120AID1346924
TDP1 proteinHomo sapiens (human)Potency6.68380.000811.382244.6684AID686978; AID686979
GLI family zinc finger 3Homo sapiens (human)Potency6.30300.000714.592883.7951AID1259369; AID1259392
AR proteinHomo sapiens (human)Potency5.90070.000221.22318,912.5098AID1259243; AID1259247; AID743035; AID743042; AID743053; AID743054; AID743063
caspase 7, apoptosis-related cysteine proteaseHomo sapiens (human)Potency33.49150.013326.981070.7614AID1346978
estrogen receptor 2 (ER beta)Homo sapiens (human)Potency20.95210.000657.913322,387.1992AID1259377; AID1259378
nuclear receptor subfamily 1, group I, member 3Homo sapiens (human)Potency17.78010.001022.650876.6163AID1224893
progesterone receptorHomo sapiens (human)Potency28.60080.000417.946075.1148AID1346784; AID1346795
cytochrome P450 family 3 subfamily A polypeptide 4Homo sapiens (human)Potency8.70900.01237.983543.2770AID1645841
glucocorticoid receptor [Homo sapiens]Homo sapiens (human)Potency25.65350.000214.376460.0339AID720691; AID720692; AID720719
retinoic acid nuclear receptor alpha variant 1Homo sapiens (human)Potency20.89830.003041.611522,387.1992AID1159552; AID1159553; AID1159555
retinoid X nuclear receptor alphaHomo sapiens (human)Potency4.77160.000817.505159.3239AID1159527; AID1159531
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency3.84750.001530.607315,848.9004AID1224841; AID1224842; AID1224848; AID1224849; AID1259401; AID1259403
farnesoid X nuclear receptorHomo sapiens (human)Potency33.48890.375827.485161.6524AID743217
pregnane X nuclear receptorHomo sapiens (human)Potency7.49780.005428.02631,258.9301AID1346982
estrogen nuclear receptor alphaHomo sapiens (human)Potency7.77140.000229.305416,493.5996AID1259244; AID1259248; AID1259383; AID743069; AID743078; AID743079; AID743080; AID743091
GVesicular stomatitis virusPotency21.87610.01238.964839.8107AID1645842
cytochrome P450 2D6Homo sapiens (human)Potency12.30180.00108.379861.1304AID1645840
peroxisome proliferator activated receptor gammaHomo sapiens (human)Potency20.52570.001019.414170.9645AID743140; AID743191
caspase-3Homo sapiens (human)Potency33.49150.013326.981070.7614AID1346978
cytochrome P450, family 19, subfamily A, polypeptide 1, isoform CRA_aHomo sapiens (human)Potency10.59090.001723.839378.1014AID743083
thyroid stimulating hormone receptorHomo sapiens (human)Potency26.60320.001628.015177.1139AID1224895
nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 (p105), isoform CRA_aHomo sapiens (human)Potency26.832519.739145.978464.9432AID1159509
v-jun sarcoma virus 17 oncogene homolog (avian)Homo sapiens (human)Potency26.83250.057821.109761.2679AID1159526; AID1159528
nuclear receptor subfamily 1, group I, member 2Rattus norvegicus (Norway rat)Potency28.18380.10009.191631.6228AID1346983
thyroid hormone receptor beta isoform aHomo sapiens (human)Potency0.08910.010039.53711,122.0200AID1479
potassium voltage-gated channel subfamily H member 2 isoform dHomo sapiens (human)Potency25.11890.01789.637444.6684AID588834
thyroid hormone receptor beta isoform 2Rattus norvegicus (Norway rat)Potency8.41270.000323.4451159.6830AID743065; AID743067
heat shock protein beta-1Homo sapiens (human)Potency33.48890.042027.378961.6448AID743210; AID743228
huntingtin isoform 2Homo sapiens (human)Potency35.48130.000618.41981,122.0200AID1688
nuclear factor erythroid 2-related factor 2 isoform 1Homo sapiens (human)Potency11.69230.000627.21521,122.0200AID743202; AID743219
nuclear receptor ROR-gamma isoform 1Mus musculus (house mouse)Potency35.48130.00798.23321,122.0200AID2546
gemininHomo sapiens (human)Potency30.05340.004611.374133.4983AID624296; AID624297
peripheral myelin protein 22Rattus norvegicus (Norway rat)Potency18.10560.005612.367736.1254AID624032
Voltage-dependent calcium channel gamma-2 subunitMus musculus (house mouse)Potency6.68240.001557.789015,848.9004AID1259244
Interferon betaHomo sapiens (human)Potency21.87610.00339.158239.8107AID1645842
HLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)Potency21.87610.01238.964839.8107AID1645842
Cellular tumor antigen p53Homo sapiens (human)Potency31.67040.002319.595674.0614AID651631; AID720552
Glutamate receptor 2Rattus norvegicus (Norway rat)Potency6.68240.001551.739315,848.9004AID1259244
Spike glycoproteinSevere acute respiratory syndrome-related coronavirusPotency10.04420.009610.525035.4813AID1479145; AID1479148
Inositol hexakisphosphate kinase 1Homo sapiens (human)Potency21.87610.01238.964839.8107AID1645842
ATPase family AAA domain-containing protein 5Homo sapiens (human)Potency2.11320.011917.942071.5630AID651632
Ataxin-2Homo sapiens (human)Potency2.11320.011912.222168.7989AID651632
cytochrome P450 2C9, partialHomo sapiens (human)Potency21.87610.01238.964839.8107AID1645842
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (185)

Processvia Protein(s)Taxonomy
cell surface receptor signaling pathway via JAK-STATInterferon betaHomo sapiens (human)
response to exogenous dsRNAInterferon betaHomo sapiens (human)
B cell activation involved in immune responseInterferon betaHomo sapiens (human)
cell surface receptor signaling pathwayInterferon betaHomo sapiens (human)
cell surface receptor signaling pathway via JAK-STATInterferon betaHomo sapiens (human)
response to virusInterferon betaHomo sapiens (human)
positive regulation of autophagyInterferon betaHomo sapiens (human)
cytokine-mediated signaling pathwayInterferon betaHomo sapiens (human)
natural killer cell activationInterferon betaHomo sapiens (human)
positive regulation of peptidyl-serine phosphorylation of STAT proteinInterferon betaHomo sapiens (human)
cellular response to interferon-betaInterferon betaHomo sapiens (human)
B cell proliferationInterferon betaHomo sapiens (human)
negative regulation of viral genome replicationInterferon betaHomo sapiens (human)
innate immune responseInterferon betaHomo sapiens (human)
positive regulation of innate immune responseInterferon betaHomo sapiens (human)
regulation of MHC class I biosynthetic processInterferon betaHomo sapiens (human)
negative regulation of T cell differentiationInterferon betaHomo sapiens (human)
positive regulation of transcription by RNA polymerase IIInterferon betaHomo sapiens (human)
defense response to virusInterferon betaHomo sapiens (human)
type I interferon-mediated signaling pathwayInterferon betaHomo sapiens (human)
neuron cellular homeostasisInterferon betaHomo sapiens (human)
cellular response to exogenous dsRNAInterferon betaHomo sapiens (human)
cellular response to virusInterferon betaHomo sapiens (human)
negative regulation of Lewy body formationInterferon betaHomo sapiens (human)
negative regulation of T-helper 2 cell cytokine productionInterferon betaHomo sapiens (human)
positive regulation of apoptotic signaling pathwayInterferon betaHomo sapiens (human)
response to exogenous dsRNAInterferon betaHomo sapiens (human)
B cell differentiationInterferon betaHomo sapiens (human)
natural killer cell activation involved in immune responseInterferon betaHomo sapiens (human)
adaptive immune responseInterferon betaHomo sapiens (human)
T cell activation involved in immune responseInterferon betaHomo sapiens (human)
humoral immune responseInterferon betaHomo sapiens (human)
positive regulation of T cell mediated cytotoxicityHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
adaptive immune responseHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
antigen processing and presentation of endogenous peptide antigen via MHC class I via ER pathway, TAP-independentHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
regulation of T cell anergyHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
defense responseHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
immune responseHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
detection of bacteriumHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
regulation of interleukin-12 productionHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
regulation of interleukin-6 productionHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
protection from natural killer cell mediated cytotoxicityHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
innate immune responseHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
regulation of dendritic cell differentiationHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
antigen processing and presentation of endogenous peptide antigen via MHC class IbHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
negative regulation of cell population proliferationCellular tumor antigen p53Homo sapiens (human)
regulation of cell cycleCellular tumor antigen p53Homo sapiens (human)
regulation of cell cycle G2/M phase transitionCellular tumor antigen p53Homo sapiens (human)
DNA damage responseCellular tumor antigen p53Homo sapiens (human)
ER overload responseCellular tumor antigen p53Homo sapiens (human)
cellular response to glucose starvationCellular tumor antigen p53Homo sapiens (human)
intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
regulation of apoptotic processCellular tumor antigen p53Homo sapiens (human)
positive regulation of transcription by RNA polymerase IICellular tumor antigen p53Homo sapiens (human)
positive regulation of miRNA transcriptionCellular tumor antigen p53Homo sapiens (human)
negative regulation of transcription by RNA polymerase IICellular tumor antigen p53Homo sapiens (human)
mitophagyCellular tumor antigen p53Homo sapiens (human)
in utero embryonic developmentCellular tumor antigen p53Homo sapiens (human)
somitogenesisCellular tumor antigen p53Homo sapiens (human)
release of cytochrome c from mitochondriaCellular tumor antigen p53Homo sapiens (human)
hematopoietic progenitor cell differentiationCellular tumor antigen p53Homo sapiens (human)
T cell proliferation involved in immune responseCellular tumor antigen p53Homo sapiens (human)
B cell lineage commitmentCellular tumor antigen p53Homo sapiens (human)
T cell lineage commitmentCellular tumor antigen p53Homo sapiens (human)
response to ischemiaCellular tumor antigen p53Homo sapiens (human)
nucleotide-excision repairCellular tumor antigen p53Homo sapiens (human)
double-strand break repairCellular tumor antigen p53Homo sapiens (human)
regulation of DNA-templated transcriptionCellular tumor antigen p53Homo sapiens (human)
regulation of transcription by RNA polymerase IICellular tumor antigen p53Homo sapiens (human)
protein import into nucleusCellular tumor antigen p53Homo sapiens (human)
autophagyCellular tumor antigen p53Homo sapiens (human)
DNA damage responseCellular tumor antigen p53Homo sapiens (human)
DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrestCellular tumor antigen p53Homo sapiens (human)
DNA damage response, signal transduction by p53 class mediator resulting in transcription of p21 class mediatorCellular tumor antigen p53Homo sapiens (human)
transforming growth factor beta receptor signaling pathwayCellular tumor antigen p53Homo sapiens (human)
Ras protein signal transductionCellular tumor antigen p53Homo sapiens (human)
gastrulationCellular tumor antigen p53Homo sapiens (human)
neuroblast proliferationCellular tumor antigen p53Homo sapiens (human)
negative regulation of neuroblast proliferationCellular tumor antigen p53Homo sapiens (human)
protein localizationCellular tumor antigen p53Homo sapiens (human)
negative regulation of DNA replicationCellular tumor antigen p53Homo sapiens (human)
negative regulation of cell population proliferationCellular tumor antigen p53Homo sapiens (human)
determination of adult lifespanCellular tumor antigen p53Homo sapiens (human)
mRNA transcriptionCellular tumor antigen p53Homo sapiens (human)
rRNA transcriptionCellular tumor antigen p53Homo sapiens (human)
response to salt stressCellular tumor antigen p53Homo sapiens (human)
response to inorganic substanceCellular tumor antigen p53Homo sapiens (human)
response to X-rayCellular tumor antigen p53Homo sapiens (human)
response to gamma radiationCellular tumor antigen p53Homo sapiens (human)
positive regulation of gene expressionCellular tumor antigen p53Homo sapiens (human)
cardiac muscle cell apoptotic processCellular tumor antigen p53Homo sapiens (human)
positive regulation of cardiac muscle cell apoptotic processCellular tumor antigen p53Homo sapiens (human)
glial cell proliferationCellular tumor antigen p53Homo sapiens (human)
viral processCellular tumor antigen p53Homo sapiens (human)
glucose catabolic process to lactate via pyruvateCellular tumor antigen p53Homo sapiens (human)
cerebellum developmentCellular tumor antigen p53Homo sapiens (human)
negative regulation of cell growthCellular tumor antigen p53Homo sapiens (human)
DNA damage response, signal transduction by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
negative regulation of transforming growth factor beta receptor signaling pathwayCellular tumor antigen p53Homo sapiens (human)
mitotic G1 DNA damage checkpoint signalingCellular tumor antigen p53Homo sapiens (human)
negative regulation of telomere maintenance via telomeraseCellular tumor antigen p53Homo sapiens (human)
T cell differentiation in thymusCellular tumor antigen p53Homo sapiens (human)
tumor necrosis factor-mediated signaling pathwayCellular tumor antigen p53Homo sapiens (human)
regulation of tissue remodelingCellular tumor antigen p53Homo sapiens (human)
cellular response to UVCellular tumor antigen p53Homo sapiens (human)
multicellular organism growthCellular tumor antigen p53Homo sapiens (human)
positive regulation of mitochondrial membrane permeabilityCellular tumor antigen p53Homo sapiens (human)
cellular response to glucose starvationCellular tumor antigen p53Homo sapiens (human)
intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
positive regulation of apoptotic processCellular tumor antigen p53Homo sapiens (human)
negative regulation of apoptotic processCellular tumor antigen p53Homo sapiens (human)
entrainment of circadian clock by photoperiodCellular tumor antigen p53Homo sapiens (human)
mitochondrial DNA repairCellular tumor antigen p53Homo sapiens (human)
regulation of DNA damage response, signal transduction by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
positive regulation of neuron apoptotic processCellular tumor antigen p53Homo sapiens (human)
transcription initiation-coupled chromatin remodelingCellular tumor antigen p53Homo sapiens (human)
negative regulation of proteolysisCellular tumor antigen p53Homo sapiens (human)
negative regulation of DNA-templated transcriptionCellular tumor antigen p53Homo sapiens (human)
positive regulation of DNA-templated transcriptionCellular tumor antigen p53Homo sapiens (human)
positive regulation of RNA polymerase II transcription preinitiation complex assemblyCellular tumor antigen p53Homo sapiens (human)
positive regulation of transcription by RNA polymerase IICellular tumor antigen p53Homo sapiens (human)
response to antibioticCellular tumor antigen p53Homo sapiens (human)
fibroblast proliferationCellular tumor antigen p53Homo sapiens (human)
negative regulation of fibroblast proliferationCellular tumor antigen p53Homo sapiens (human)
circadian behaviorCellular tumor antigen p53Homo sapiens (human)
bone marrow developmentCellular tumor antigen p53Homo sapiens (human)
embryonic organ developmentCellular tumor antigen p53Homo sapiens (human)
positive regulation of peptidyl-tyrosine phosphorylationCellular tumor antigen p53Homo sapiens (human)
protein stabilizationCellular tumor antigen p53Homo sapiens (human)
negative regulation of helicase activityCellular tumor antigen p53Homo sapiens (human)
protein tetramerizationCellular tumor antigen p53Homo sapiens (human)
chromosome organizationCellular tumor antigen p53Homo sapiens (human)
neuron apoptotic processCellular tumor antigen p53Homo sapiens (human)
regulation of cell cycleCellular tumor antigen p53Homo sapiens (human)
hematopoietic stem cell differentiationCellular tumor antigen p53Homo sapiens (human)
negative regulation of glial cell proliferationCellular tumor antigen p53Homo sapiens (human)
type II interferon-mediated signaling pathwayCellular tumor antigen p53Homo sapiens (human)
cardiac septum morphogenesisCellular tumor antigen p53Homo sapiens (human)
positive regulation of programmed necrotic cell deathCellular tumor antigen p53Homo sapiens (human)
protein-containing complex assemblyCellular tumor antigen p53Homo sapiens (human)
intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stressCellular tumor antigen p53Homo sapiens (human)
thymocyte apoptotic processCellular tumor antigen p53Homo sapiens (human)
positive regulation of thymocyte apoptotic processCellular tumor antigen p53Homo sapiens (human)
necroptotic processCellular tumor antigen p53Homo sapiens (human)
cellular response to hypoxiaCellular tumor antigen p53Homo sapiens (human)
cellular response to xenobiotic stimulusCellular tumor antigen p53Homo sapiens (human)
cellular response to ionizing radiationCellular tumor antigen p53Homo sapiens (human)
cellular response to gamma radiationCellular tumor antigen p53Homo sapiens (human)
cellular response to UV-CCellular tumor antigen p53Homo sapiens (human)
stem cell proliferationCellular tumor antigen p53Homo sapiens (human)
signal transduction by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
intrinsic apoptotic signaling pathway by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
reactive oxygen species metabolic processCellular tumor antigen p53Homo sapiens (human)
cellular response to actinomycin DCellular tumor antigen p53Homo sapiens (human)
positive regulation of release of cytochrome c from mitochondriaCellular tumor antigen p53Homo sapiens (human)
cellular senescenceCellular tumor antigen p53Homo sapiens (human)
replicative senescenceCellular tumor antigen p53Homo sapiens (human)
oxidative stress-induced premature senescenceCellular tumor antigen p53Homo sapiens (human)
intrinsic apoptotic signaling pathwayCellular tumor antigen p53Homo sapiens (human)
oligodendrocyte apoptotic processCellular tumor antigen p53Homo sapiens (human)
positive regulation of execution phase of apoptosisCellular tumor antigen p53Homo sapiens (human)
negative regulation of mitophagyCellular tumor antigen p53Homo sapiens (human)
regulation of mitochondrial membrane permeability involved in apoptotic processCellular tumor antigen p53Homo sapiens (human)
regulation of intrinsic apoptotic signaling pathway by p53 class mediatorCellular tumor antigen p53Homo sapiens (human)
positive regulation of miRNA transcriptionCellular tumor antigen p53Homo sapiens (human)
negative regulation of G1 to G0 transitionCellular tumor antigen p53Homo sapiens (human)
negative regulation of miRNA processingCellular tumor antigen p53Homo sapiens (human)
negative regulation of glucose catabolic process to lactate via pyruvateCellular tumor antigen p53Homo sapiens (human)
negative regulation of pentose-phosphate shuntCellular tumor antigen p53Homo sapiens (human)
intrinsic apoptotic signaling pathway in response to hypoxiaCellular tumor antigen p53Homo sapiens (human)
regulation of fibroblast apoptotic processCellular tumor antigen p53Homo sapiens (human)
negative regulation of reactive oxygen species metabolic processCellular tumor antigen p53Homo sapiens (human)
positive regulation of reactive oxygen species metabolic processCellular tumor antigen p53Homo sapiens (human)
negative regulation of stem cell proliferationCellular tumor antigen p53Homo sapiens (human)
positive regulation of cellular senescenceCellular tumor antigen p53Homo sapiens (human)
positive regulation of intrinsic apoptotic signaling pathwayCellular tumor antigen p53Homo sapiens (human)
inositol phosphate metabolic processInositol hexakisphosphate kinase 1Homo sapiens (human)
phosphatidylinositol phosphate biosynthetic processInositol hexakisphosphate kinase 1Homo sapiens (human)
negative regulation of cold-induced thermogenesisInositol hexakisphosphate kinase 1Homo sapiens (human)
inositol phosphate biosynthetic processInositol hexakisphosphate kinase 1Homo sapiens (human)
cell population proliferationATPase family AAA domain-containing protein 5Homo sapiens (human)
positive regulation of B cell proliferationATPase family AAA domain-containing protein 5Homo sapiens (human)
nuclear DNA replicationATPase family AAA domain-containing protein 5Homo sapiens (human)
signal transduction in response to DNA damageATPase family AAA domain-containing protein 5Homo sapiens (human)
intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediatorATPase family AAA domain-containing protein 5Homo sapiens (human)
isotype switchingATPase family AAA domain-containing protein 5Homo sapiens (human)
positive regulation of DNA replicationATPase family AAA domain-containing protein 5Homo sapiens (human)
positive regulation of isotype switching to IgG isotypesATPase family AAA domain-containing protein 5Homo sapiens (human)
DNA clamp unloadingATPase family AAA domain-containing protein 5Homo sapiens (human)
regulation of mitotic cell cycle phase transitionATPase family AAA domain-containing protein 5Homo sapiens (human)
negative regulation of intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediatorATPase family AAA domain-containing protein 5Homo sapiens (human)
positive regulation of cell cycle G2/M phase transitionATPase family AAA domain-containing protein 5Homo sapiens (human)
negative regulation of receptor internalizationAtaxin-2Homo sapiens (human)
regulation of translationAtaxin-2Homo sapiens (human)
RNA metabolic processAtaxin-2Homo sapiens (human)
P-body assemblyAtaxin-2Homo sapiens (human)
stress granule assemblyAtaxin-2Homo sapiens (human)
RNA transportAtaxin-2Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (55)

Processvia Protein(s)Taxonomy
cytokine activityInterferon betaHomo sapiens (human)
cytokine receptor bindingInterferon betaHomo sapiens (human)
type I interferon receptor bindingInterferon betaHomo sapiens (human)
protein bindingInterferon betaHomo sapiens (human)
chloramphenicol O-acetyltransferase activityInterferon betaHomo sapiens (human)
TAP bindingHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
signaling receptor bindingHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
protein bindingHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
peptide antigen bindingHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
TAP bindingHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
protein-folding chaperone bindingHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
transcription cis-regulatory region bindingCellular tumor antigen p53Homo sapiens (human)
RNA polymerase II cis-regulatory region sequence-specific DNA bindingCellular tumor antigen p53Homo sapiens (human)
DNA-binding transcription factor activity, RNA polymerase II-specificCellular tumor antigen p53Homo sapiens (human)
cis-regulatory region sequence-specific DNA bindingCellular tumor antigen p53Homo sapiens (human)
core promoter sequence-specific DNA bindingCellular tumor antigen p53Homo sapiens (human)
TFIID-class transcription factor complex bindingCellular tumor antigen p53Homo sapiens (human)
DNA-binding transcription repressor activity, RNA polymerase II-specificCellular tumor antigen p53Homo sapiens (human)
DNA-binding transcription activator activity, RNA polymerase II-specificCellular tumor antigen p53Homo sapiens (human)
protease bindingCellular tumor antigen p53Homo sapiens (human)
p53 bindingCellular tumor antigen p53Homo sapiens (human)
DNA bindingCellular tumor antigen p53Homo sapiens (human)
chromatin bindingCellular tumor antigen p53Homo sapiens (human)
DNA-binding transcription factor activityCellular tumor antigen p53Homo sapiens (human)
mRNA 3'-UTR bindingCellular tumor antigen p53Homo sapiens (human)
copper ion bindingCellular tumor antigen p53Homo sapiens (human)
protein bindingCellular tumor antigen p53Homo sapiens (human)
zinc ion bindingCellular tumor antigen p53Homo sapiens (human)
enzyme bindingCellular tumor antigen p53Homo sapiens (human)
receptor tyrosine kinase bindingCellular tumor antigen p53Homo sapiens (human)
ubiquitin protein ligase bindingCellular tumor antigen p53Homo sapiens (human)
histone deacetylase regulator activityCellular tumor antigen p53Homo sapiens (human)
ATP-dependent DNA/DNA annealing activityCellular tumor antigen p53Homo sapiens (human)
identical protein bindingCellular tumor antigen p53Homo sapiens (human)
histone deacetylase bindingCellular tumor antigen p53Homo sapiens (human)
protein heterodimerization activityCellular tumor antigen p53Homo sapiens (human)
protein-folding chaperone bindingCellular tumor antigen p53Homo sapiens (human)
protein phosphatase 2A bindingCellular tumor antigen p53Homo sapiens (human)
RNA polymerase II-specific DNA-binding transcription factor bindingCellular tumor antigen p53Homo sapiens (human)
14-3-3 protein bindingCellular tumor antigen p53Homo sapiens (human)
MDM2/MDM4 family protein bindingCellular tumor antigen p53Homo sapiens (human)
disordered domain specific bindingCellular tumor antigen p53Homo sapiens (human)
general transcription initiation factor bindingCellular tumor antigen p53Homo sapiens (human)
molecular function activator activityCellular tumor antigen p53Homo sapiens (human)
promoter-specific chromatin bindingCellular tumor antigen p53Homo sapiens (human)
inositol-1,3,4,5,6-pentakisphosphate kinase activityInositol hexakisphosphate kinase 1Homo sapiens (human)
inositol hexakisphosphate kinase activityInositol hexakisphosphate kinase 1Homo sapiens (human)
inositol heptakisphosphate kinase activityInositol hexakisphosphate kinase 1Homo sapiens (human)
inositol hexakisphosphate 5-kinase activityInositol hexakisphosphate kinase 1Homo sapiens (human)
protein bindingInositol hexakisphosphate kinase 1Homo sapiens (human)
ATP bindingInositol hexakisphosphate kinase 1Homo sapiens (human)
inositol hexakisphosphate 1-kinase activityInositol hexakisphosphate kinase 1Homo sapiens (human)
inositol hexakisphosphate 3-kinase activityInositol hexakisphosphate kinase 1Homo sapiens (human)
inositol 5-diphosphate pentakisphosphate 5-kinase activityInositol hexakisphosphate kinase 1Homo sapiens (human)
inositol diphosphate tetrakisphosphate kinase activityInositol hexakisphosphate kinase 1Homo sapiens (human)
protein bindingATPase family AAA domain-containing protein 5Homo sapiens (human)
ATP bindingATPase family AAA domain-containing protein 5Homo sapiens (human)
ATP hydrolysis activityATPase family AAA domain-containing protein 5Homo sapiens (human)
DNA clamp unloader activityATPase family AAA domain-containing protein 5Homo sapiens (human)
DNA bindingATPase family AAA domain-containing protein 5Homo sapiens (human)
RNA bindingAtaxin-2Homo sapiens (human)
epidermal growth factor receptor bindingAtaxin-2Homo sapiens (human)
protein bindingAtaxin-2Homo sapiens (human)
mRNA bindingAtaxin-2Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (42)

Processvia Protein(s)Taxonomy
extracellular spaceInterferon betaHomo sapiens (human)
extracellular regionInterferon betaHomo sapiens (human)
Golgi membraneHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
endoplasmic reticulumHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
Golgi apparatusHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
plasma membraneHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
cell surfaceHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
ER to Golgi transport vesicle membraneHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
membraneHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
secretory granule membraneHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
phagocytic vesicle membraneHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
early endosome membraneHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
recycling endosome membraneHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
extracellular exosomeHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
lumenal side of endoplasmic reticulum membraneHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
MHC class I protein complexHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
extracellular spaceHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
external side of plasma membraneHLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)
nuclear bodyCellular tumor antigen p53Homo sapiens (human)
nucleusCellular tumor antigen p53Homo sapiens (human)
nucleoplasmCellular tumor antigen p53Homo sapiens (human)
replication forkCellular tumor antigen p53Homo sapiens (human)
nucleolusCellular tumor antigen p53Homo sapiens (human)
cytoplasmCellular tumor antigen p53Homo sapiens (human)
mitochondrionCellular tumor antigen p53Homo sapiens (human)
mitochondrial matrixCellular tumor antigen p53Homo sapiens (human)
endoplasmic reticulumCellular tumor antigen p53Homo sapiens (human)
centrosomeCellular tumor antigen p53Homo sapiens (human)
cytosolCellular tumor antigen p53Homo sapiens (human)
nuclear matrixCellular tumor antigen p53Homo sapiens (human)
PML bodyCellular tumor antigen p53Homo sapiens (human)
transcription repressor complexCellular tumor antigen p53Homo sapiens (human)
site of double-strand breakCellular tumor antigen p53Homo sapiens (human)
germ cell nucleusCellular tumor antigen p53Homo sapiens (human)
chromatinCellular tumor antigen p53Homo sapiens (human)
transcription regulator complexCellular tumor antigen p53Homo sapiens (human)
protein-containing complexCellular tumor antigen p53Homo sapiens (human)
plasma membraneGlutamate receptor 2Rattus norvegicus (Norway rat)
virion membraneSpike glycoproteinSevere acute respiratory syndrome-related coronavirus
fibrillar centerInositol hexakisphosphate kinase 1Homo sapiens (human)
nucleoplasmInositol hexakisphosphate kinase 1Homo sapiens (human)
cytosolInositol hexakisphosphate kinase 1Homo sapiens (human)
nucleusInositol hexakisphosphate kinase 1Homo sapiens (human)
cytoplasmInositol hexakisphosphate kinase 1Homo sapiens (human)
Elg1 RFC-like complexATPase family AAA domain-containing protein 5Homo sapiens (human)
nucleusATPase family AAA domain-containing protein 5Homo sapiens (human)
cytoplasmAtaxin-2Homo sapiens (human)
Golgi apparatusAtaxin-2Homo sapiens (human)
trans-Golgi networkAtaxin-2Homo sapiens (human)
cytosolAtaxin-2Homo sapiens (human)
cytoplasmic stress granuleAtaxin-2Homo sapiens (human)
membraneAtaxin-2Homo sapiens (human)
perinuclear region of cytoplasmAtaxin-2Homo sapiens (human)
ribonucleoprotein complexAtaxin-2Homo sapiens (human)
cytoplasmic stress granuleAtaxin-2Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (54)

Assay IDTitleYearJournalArticle
AID1347124qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for RD cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347110qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for A673 cells)2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347102qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Rh18 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347106qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for control Hh wild type fibroblast cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347129qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for SK-N-SH cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347113qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for LAN-5 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347094qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for BT-37 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347154Primary screen GU AMC qHTS for Zika virus inhibitors2020Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors.
AID1347109qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for NB1643 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347425Rhodamine-PBP qHTS Assay for Modulators of WT P53-Induced Phosphatase 1 (WIP1)2019The Journal of biological chemistry, 11-15, Volume: 294, Issue:46
Physiologically relevant orthogonal assays for the discovery of small-molecule modulators of WIP1 phosphatase in high-throughput screens.
AID1347108qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Rh41 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347121qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for control Hh wild type fibroblast cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347093qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SK-N-MC cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347118qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for TC32 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1296008Cytotoxic Profiling of Annotated Libraries Using Quantitative High-Throughput Screening2020SLAS discovery : advancing life sciences R & D, 01, Volume: 25, Issue:1
Cytotoxic Profiling of Annotated and Diverse Chemical Libraries Using Quantitative High-Throughput Screening.
AID1347127qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for Saos-2 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347099qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for NB1643 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347122qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for U-2 OS cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347103qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for OHS-50 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347096qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for U-2 OS cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347086qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lymphocytic Choriomeningitis Arenaviruses (LCMV): LCMV Primary Screen - GLuc reporter signal2020Antiviral research, 01, Volume: 173A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity.
AID1347111qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for SK-N-MC cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID651635Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression
AID1347098qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SK-N-SH cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347091qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SJ-GBM2 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347107qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Rh30 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347116qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for SJ-GBM2 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347104qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for RD cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347114qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for DAOY cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347101qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for BT-12 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347119qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for MG 63 (6-TG R) cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347128qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for OHS-50 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347090qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for DAOY cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347082qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lassa (LASV) Arenavirus: LASV Primary Screen - GLuc reporter signal2020Antiviral research, 01, Volume: 173A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity.
AID1347097qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Saos-2 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347083qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lassa (LASV) Arenavirus: Viability assay - alamar blue signal for LASV Primary Screen2020Antiviral research, 01, Volume: 173A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity.
AID1347424RapidFire Mass Spectrometry qHTS Assay for Modulators of WT P53-Induced Phosphatase 1 (WIP1)2019The Journal of biological chemistry, 11-15, Volume: 294, Issue:46
Physiologically relevant orthogonal assays for the discovery of small-molecule modulators of WIP1 phosphatase in high-throughput screens.
AID1347126qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for Rh30 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347112qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for BT-12 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347115qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for NB-EBc1 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347100qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for LAN-5 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347117qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for BT-37 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347123qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for Rh41 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347095qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for NB-EBc1 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1745845Primary qHTS for Inhibitors of ATXN expression
AID1347092qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for A673 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347089qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for TC32 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1508630Primary qHTS for small molecule stabilizers of the endoplasmic reticulum resident proteome: Secreted ER Calcium Modulated Protein (SERCaMP) assay2021Cell reports, 04-27, Volume: 35, Issue:4
A target-agnostic screen identifies approved drugs to stabilize the endoplasmic reticulum-resident proteome.
AID1347407qHTS to identify inhibitors of the type 1 interferon - major histocompatibility complex class I in skeletal muscle: primary screen against the NCATS Pharmaceutical Collection2020ACS chemical biology, 07-17, Volume: 15, Issue:7
High-Throughput Screening to Identify Inhibitors of the Type I Interferon-Major Histocompatibility Complex Class I Pathway in Skeletal Muscle.
AID1347105qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for MG 63 (6-TG R) cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347125qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for Rh18 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID504749qHTS profiling for inhibitors of Plasmodium falciparum proliferation2011Science (New York, N.Y.), Aug-05, Volume: 333, Issue:6043
Chemical genomic profiling for antimalarial therapies, response signatures, and molecular targets.
AID1346987P-glycoprotein substrates identified in KB-8-5-11 adenocarcinoma cell line, qHTS therapeutic library screen2019Molecular pharmacology, 11, Volume: 96, Issue:5
A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
AID1346986P-glycoprotein substrates identified in KB-3-1 adenocarcinoma cell line, qHTS therapeutic library screen2019Molecular pharmacology, 11, Volume: 96, Issue:5
A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (1,166)

TimeframeStudies, This Drug (%)All Drugs %
pre-1990189 (16.21)18.7374
1990's260 (22.30)18.2507
2000's265 (22.73)29.6817
2010's307 (26.33)24.3611
2020's145 (12.44)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 66.11

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be very strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index66.11 (24.57)
Research Supply Index7.25 (2.92)
Research Growth Index4.71 (4.65)
Search Engine Demand Index116.11 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (66.11)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials167 (13.45%)5.53%
Reviews66 (5.31%)6.00%
Case Studies179 (14.41%)4.05%
Observational10 (0.81%)0.25%
Other820 (66.02%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Clinical Trials (41)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
TENDOSHOCK-2010 - Combined Sclerosing Therapy, Extracorporeal Shockwave Therapy, Eccentric Training and Topical Glyceryl Trinitrate for Athletic Tendinopathies [NCT01185951]Phase 2114 participants (Actual)Interventional2007-01-31Active, not recruiting
A Multicentre, Open-label, Single-arm Phase II Trial on the Efficacy and Safety of Sclerotherapy Using 3% Polidocanol Foam to Treat Second-degree Hemorrhoidal Disease [NCT03791775]Phase 2183 participants (Actual)Interventional2019-01-02Completed
Outcomes of Sclerotherapy of the Ulcer Bed Compared to a Combination of Ablation and Injections [NCT05633277]30 participants (Anticipated)Interventional2020-09-30Recruiting
An Assessment of Intra-lesional 3% Polidocanol Solution in the Treatment of Digital Myxoid Cysts [NCT02154789]Phase 4120 participants (Anticipated)Interventional2014-06-30Not yet recruiting
Observational Study of the Effect of VarIthena® on Wound Healing in the Treatment of Venous Leg Ulcers Resulting From Chronic Venous Insufficiency [NCT03257254]76 participants (Actual)Observational [Patient Registry]2017-09-29Completed
Endoscopic Cyanoacrylate Injection vs. Balloon-occluded Retrograde Transvenous Obliteration in the Prevention of Gastric Variceal Rebleeding [NCT02468206]64 participants (Actual)Interventional2015-06-30Completed
Sclerotherapy With Polidocanol Foam In The Management Of First, Second And Third-Grade Hemorrhoidal Disease In Patients With Bleeding Disorders: A Prospective Cohort Study [NCT04188171]Phase 2/Phase 3150 participants (Anticipated)Interventional2018-08-01Active, not recruiting
Primary Prophylaxis of Gastric Variceal Bleed: Endoscopic Cyanoacrylate Injection Versus Balloon-occluded Retrograde Transvenous Obliteration [NCT02468180]70 participants (Anticipated)Interventional2015-06-30Recruiting
Lord´s Procedure Versus Sclerotherapy for Testicular Hydrocele; a Randomized Controlled Study. [NCT02082613]200 participants (Anticipated)Interventional2015-02-28Recruiting
Long-term Follow-up of Sclerotherapy of Reticular Veins and Telangiectasias [NCT05860439]191 participants (Actual)Observational2017-01-01Completed
Sclerotherapy With Polidocanol Foam Versus Rubber Band Ligation in the Treatment of First, Second and Third-Grade Hemorrhoidal Disease: a Randomized, Controlled Trial [NCT04091763]Phase 2120 participants (Actual)Interventional2018-08-01Completed
Pilot Randomised Controlled Trial Evaluating the Potential Benefit of a One Stop Vein Clinic (OSVeC) [NCT02557542]5 participants (Actual)Interventional2015-10-31Terminated(stopped due to Very poor recruitment)
Comparison of Surgery Versus Foam Sclerotherapy for Isolated Accessory Great Saphenous Vein Varicosis [NCT02010723]Phase 440 participants (Actual)Interventional2006-06-30Completed
"A Randomized, Blinded, Multicenter Study to Evaluate the Efficacy and Safety of Varisolve Polidocanol Endovenous Microfoam (PEM) 0.5% and 1% Compared to Vehicle for the Treatment on Saphenofemoral Junction (SFJ) Incompetence VANISH-2" [NCT01231373]Phase 3235 participants (Actual)Interventional2010-11-30Completed
A Randomized, Blinded, Multicenter Study to Evaluate the Efficacy and Safety of Polidocanol Injectable Foam 0.5%, 1.0%, or 2.0% Compared to Vehicle for the Treatment of Saphenofemoral Junction (SFJ) Incompetence [NCT01072877]Phase 3279 participants (Actual)Interventional2010-12-31Completed
Sclerotherapy With Polidocanol Foam in the Treatment of First, Second and Third-Grade Hemorrhoidal Disease in Patients With Liver Cirrhosis: A Prospective, Cohort Trial [NCT05807425]Phase 2/Phase 340 participants (Anticipated)Interventional2023-03-31Recruiting
A Phase 4 Randomized Trial Comparing Varithena to Endothermal Ablation for the Treatment of the Great Saphenous Vein [NCT05312970]Phase 4100 participants (Anticipated)Interventional2023-02-10Recruiting
Sclerotherapy With Polidocanol Foam Versus Hemorrhoidal Artery Ligation With Recto Anal Repair in the Treatment of Second and Third-grade Hemorrhoidal Disease: a Prospective Study [NCT04675177]Phase 2/Phase 345 participants (Actual)Interventional2019-09-01Completed
Treatment of Greater Saphenous Vein (GSV) Insufficiency Using Echo-Guided Sclerotherapy With Lauromacrogol 400 Foam -Comparative Study of 3% Versus 1% Concentration. [NCT00348764]Phase 3150 participants Interventional2004-03-31Completed
Three-year Outcomes of a RCT Comparing EVLA Versus Polidocanol Foam in the Treatment of SSV Insufficiency (FOVELASS Study, by the French Society of Phlebology) [NCT05468450]161 participants (Actual)Interventional2015-07-01Completed
A Multicenter Prospective Clinical Study of Endoscopic Foam Sclerotherapy for Internal Hemorrhoids [NCT04398823]Phase 4700 participants (Anticipated)Interventional2020-05-15Recruiting
Placebo Controlled Trial, Testing the Efficacy of Polidocanol Injections as a Treatment of Chronic Achilles Tendinopathy. [NCT00377910]Phase 448 participants (Actual)Interventional2008-03-31Completed
Preliminary Study on Submucous Sclerosis of Pharynges With 1% Polidocanol to Treat Obstructive Sleep Apnea (OSA) & Snoring Subjects (SS) [NCT00399451]Phase 1/Phase 230 participants Interventional2006-12-31Not yet recruiting
Effect of Polidocanol Endovenous Microfoam (PEM) Treatment of Superficial Axial and Tributary Vein Reflux on Improvement of Wound Healing in Venous Leg Ulcers (VLUs) [NCT02988063]Phase 40 participants (Actual)Interventional2017-04-10Withdrawn(stopped due to Poor enrollment)
Intralesional Sclerosant for in Transit and Cutaneous Melanoma Metastases [NCT03754140]Phase 20 participants (Actual)Interventional2020-05-20Withdrawn(stopped due to Unable to identify eligible patients within planned timeframe)
A Multicenter, Randomized, Blinded Study of Endovenous Thermal Ablation With or Without Varisolve™ Polidocanol Endovenous Microfoam (PEM) Treatment for Patients With Great Saphenous Vein Incompetence and Visible Varicosities [NCT01197833]Phase 3117 participants (Actual)Interventional2010-09-30Completed
A Randomized Comparison of Flexible Endoscopic Polidocanol Liquid and Foam Sclerotherapy in Cirrhotic Patients With Bleeding From Internal Hemorrhoids [NCT06031740]60 participants (Anticipated)Interventional2023-09-07Not yet recruiting
Endovascular Versus Medical Treatment for the Pelvic Congestion Syndrome [NCT04358497]Phase 4120 participants (Anticipated)Interventional2020-10-01Not yet recruiting
An Open-label, Single-dose Pilot Study to Evaluate the Efficacy and Safety of Varisolve® (Polidocanol Endovenous Microfoam) 0.125% [0.2%] for the Treatment of Symptomatic, Visible Varicose Veins With Saphenofemoral Junction (SFJ) Incompetence [NCT00928421]Phase 216 participants (Actual)Interventional2009-06-30Completed
Treatment of Venous Malformation by Direct Puncture Repair: Ethanol Versus Polidocanol [NCT05586919]20 participants (Actual)Interventional2018-10-01Completed
Polidocanol Versus Glucose For Sclerotherapy Treatment Of Telangiectasia Of The Lower Limbs: Protocol For A Randomized, Controlled Clinical Trial [NCT02657252]Phase 4115 participants (Actual)Interventional2015-01-31Completed
Comparative Study of Polidocanol and Absolute Alcohol for Percutaneous Ultrasound Guided Treatment of Benign Thyroid Cyst [NCT05798936]Phase 430 participants (Anticipated)Interventional2023-04-01Not yet recruiting
An Open Label Multicenter Safety Study of the Varisolve® Procedure for the Treatment of Varicose Veins in Patients With Right-to-left Cardiac Shunt [NCT00442364]Phase 260 participants (Actual)Interventional2007-03-31Completed
A Randomized Study to Compare Effect of Endoscopic Injection of a Mixture of Cyanoacrylate and Lipiodol Versus Cyanoacrylate and Lauromacrogol in Gastric Varices [NCT01923064]96 participants (Actual)Interventional2013-10-31Completed
Efficacy of Skin Cooling in Reducing Pain Associated With Non-invasive Treatments of Neurofibromatosis Type 1 Cutaneous Neurofibromas [NCT06132165]Phase 130 participants (Anticipated)Interventional2023-12-01Not yet recruiting
Endoscopic Ultrasound-guided Fine-needle Injection for Nonfunctional Pancreatic Neuroendocrine Tumors: a Prospective Multicenter Study [NCT05566093]20 participants (Anticipated)Interventional2018-09-28Recruiting
A Randomized, Single Blind, Placebo Controlled, Multicenter Study to Evaluate Efficacy and Safety of Polidocanol Injectable Foam for the Treatment of Symptomatic, Visible Varicose Veins With Saphenofemoral Junction (SFJ) Incompetence. [NCT00758420]Phase 2/Phase 377 participants (Actual)Interventional2008-10-31Completed
An Open-Label Single-Center Study in Patients With Great Saphenous Vein Incompetence to Investigate the Pharmacokinetic Properties of Polidocanol Endovenous Microfoam (PEM) [NCT01428076]Phase 121 participants (Actual)Interventional2011-08-31Completed
Multicenter Study to Evaluate Pain Following Treatment of Varicose Vein With Varithena® Compared to Radiofrequency Ablation [NCT02462720]Phase 435 participants (Actual)Interventional2015-05-31Completed
Comparison of Endoscopic Cyanoacrylate Injection Versus Balloon-occluded Retrograde Transvenous Obliteration in the Management of Acute Gastric Variceal Bleeding [NCT02468167]70 participants (Anticipated)Interventional2015-06-30Recruiting
A Randomized Triple-blind Study Protocol Comparing Polidocanol Versus Hypertonic Glucose for Sclerotherapy in Treatment of Reticular Veins at the Lower Limbs. [NCT02054325]Phase 4106 participants (Actual)Interventional2012-09-30Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

TrialOutcome
NCT00442364 (1) [back to overview]Patients With Circulating MCA Bubbles Present on MRI Who Had Signficant Clinical or Neurological Effects
NCT00758420 (1) [back to overview]The Absolute Change From Baseline Score for the VVSymQ (Total Score) at 8 Weeks
NCT00928421 (1) [back to overview]Responders to Treatment, Assessed by Duplex Ultrasound
NCT01072877 (3) [back to overview]Change From Baseline at 8 Weeks Post Treatment in IPR-V3 Score- Physician Photographic Review of Appearance
NCT01072877 (3) [back to overview]Change From Baseline to 8 Weeks in Appearance as Rated by Patient (PA-V3)
NCT01072877 (3) [back to overview]Change in Patient-reported Symptoms of Varicose Veins (VVSymQ Score)
NCT01197833 (2) [back to overview]Absolute Change From Baseline in Independent Photography Review (IPR-V3 Score)
NCT01197833 (2) [back to overview]Absolute Change From Baseline in PA-V3 Score
NCT01231373 (3) [back to overview]Change From Baseline at 8 Weeks Post-Treatment in IPR-V3 Score--Physician Photographic Review of Appearance
NCT01231373 (3) [back to overview]Change From Baseline to 8 Weeks in Appearance as Rated by Patient (PA-V3)
NCT01231373 (3) [back to overview]Change in Patient-Reported Symptoms of Varicose Veins (VVSymQ Score)
NCT01428076 (1) [back to overview]Weight-adjusted Polidocanol Cmax (Serum)
NCT02054325 (2) [back to overview]Efficacy in Treating Reticular Veins by Photographs: Mean Percent Reticular Vein Disappearance Two Months After Treatment.
NCT02054325 (2) [back to overview]The Safety of the Treatment: Mean Percent of Skin Hyperpigmentation Two Months After Treatment
NCT02462720 (3) [back to overview]Pain
NCT02462720 (3) [back to overview]Patient Preference
NCT02462720 (3) [back to overview]Procedural Pain
NCT02657252 (3) [back to overview]Change From Baseline in Extent of Telangiectasias
NCT02657252 (3) [back to overview]Number of Participants With Deep Venous Thrombosis (DVT)
NCT02657252 (3) [back to overview]Skin Hyperpigmentation
NCT03257254 (9) [back to overview]Number of Ulcer Free Days
NCT03257254 (9) [back to overview]Number of Wound Closure at 12 Weeks
NCT03257254 (9) [back to overview]Number of Wound Recurrences
NCT03257254 (9) [back to overview]Number of Wounds Remaining Closed at 3 Months Post-wound Closure Date
NCT03257254 (9) [back to overview]Time to Wound Closure
NCT03257254 (9) [back to overview]Change From Baseline in Wound Perimeter
NCT03257254 (9) [back to overview]Change in Pain
NCT03257254 (9) [back to overview]Change in VCSS
NCT03257254 (9) [back to overview]Change on EQ-5D-5L Quality of Life Assessment

Patients With Circulating MCA Bubbles Present on MRI Who Had Signficant Clinical or Neurological Effects

(NCT00442364)
Timeframe: 28 day followup

Interventionparticipants (Number)
Safety Evaluable Population0

[back to top]

The Absolute Change From Baseline Score for the VVSymQ (Total Score) at 8 Weeks

The VVSymQ is a subset of the VEINES-Sym and consists of the 5 symptoms most relevant to patients. The raw score, which can range from 5 to 30, was transformed to a summary VVSymQ score that ranges from 0 (worst possible symptom health) to 100 (best symptom health) using the following formula: VVSymQ: (Transformed Score) = [(Raw Score) - 5] * 4. (NCT00758420)
Timeframe: Baseline to 8 weeks

Interventionunits on a scale (Least Squares Mean)
Placebo16.7
Polidocanol Injectable Foam, 1.0%30.7

[back to top]

Responders to Treatment, Assessed by Duplex Ultrasound

Responders; elimination of reflux through the saphenofemoral junction and/or coplete occlusion of the great saphenous vein at 8 weeks, as measured by duplex ultrasound. (NCT00928421)
Timeframe: 8 weeks

Interventionparticipants (Number)
Polidocanol Injectable Foam 0.125%9

[back to top]

Change From Baseline at 8 Weeks Post Treatment in IPR-V3 Score- Physician Photographic Review of Appearance

The Independent Photography Review - Visible Varicose Veins (IPR-V3) instrument is a 5-point scale used to assess the appearance of a patient's visible varicose veins. At baseline and Week 8, standardized digital photographs were taken of the medial view of the patient's target leg, from groin to ankle. An independent photography review panel, consisting of 3 trained, blinded clinicians evaluated the appearance of the patient's visible varicose veins using the IPR-V3 instrument's 5-point scale (where 0=none to 4=very severe visible varicose veins). (NCT01072877)
Timeframe: 8 weeks post treatment

Interventionunits on a scale (Mean)
Vehicle-0.01
Polidocanol Injectable Foam 0.125%-0.46
Polidocanol Injectable Foam 0.5%-0.77
Polidocanol Injectable Foam 1.0%-0.76
Polidocanol Injectable Foam 2.0%-0.91

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Change From Baseline to 8 Weeks in Appearance as Rated by Patient (PA-V3)

"The Patient Self-assessment of Visible Varicose Veins (PA-V3) instrument is a 5-point scale used by patients to evaluate the appearance of their visible varicose veins. On this single-item paper questionnaire, the instructions included a diagram of the medial view of a leg with the area between the ankle and the groin circled. The patient was instructed to choose 1 of 5 response options that best described the appearance of the visible varicose veins of the leg that was treated in the study. The patient was instructed not to consider the appearance of the leg outside the circled area or of any spider veins. Possible responses ranged from Not at all noticeable (a score of 0) to Extremely noticeable (a score of 4)." (NCT01072877)
Timeframe: 8 weeks

Interventionunits on a scale (Mean)
Vehicle-0.15
Polidocanol Injectable Foam 0.125%-0.93
Polidocanol Injectable Foam 0.5%-1.40
Polidocanol Injectable Foam 1.0%-1.60
Polidocanol Injectable Foam 2.0%-1.75

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Change in Patient-reported Symptoms of Varicose Veins (VVSymQ Score)

"The 9 varicose vein symptoms were to be assessed and graded on a 6-point (i.e., 0-5) duration scale and an 11-point (i.e., 0-10) intensity scale, and the patient's level of activity for that day was to be assessed and graded on the 6-point (i.e., 0-5) duration scale. The 9 varicose vein symptoms assessed using the e-diary were derived from the first question of the modified Venous Insufficiency Epidemiologic and Economic Study-Quality of Life/Symptoms (VEINES-QOL/Sym) instrument. The VVSymQ is a subset of 5 VEINESQOL/ Sym items that have been determined in earlier studies to be most important to patients (heaviness, achiness, swelling, throbbing, and itching).~The daily VVSymQ score is the sum of the duration scores for these 5 symptoms (scores range from 0 to 25, with the lower end of the range being an indicator of less symptom intensity, and the higher end being an indicator of higher intensity).~At Visit 2/baseline, Week 8, scores were calculated" (NCT01072877)
Timeframe: Week 8

Interventionunits on a scale (Mean)
Vehicle2.13
Polidocanol Injectable Foam 0.125%4.63
Polidocanol Injectable Foam 0.5%5.68
Polidocanol Injectable Foam 1.0%4.87
Polidocanol Injectable Foam 2.0%5.78

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Absolute Change From Baseline in Independent Photography Review (IPR-V3 Score)

The Independent Photography Review - Visible Varicose Veins (IPR-V3) instrument is a 5-point scale used to assess the appearance of a patient's visible varicose veins. At screening, the site clinician was instructed to review the appearance of the patient's varicose veins in the medial section of each leg (a 'live' assessment), then select an IPR-V3 score (i.e., none=0, mild, moderate, severe or very severe=4) that best represented the appearance of the patient's varicose veins. This assessment took into account the attributes caliber, dilatation, tortuosity, and extent and number of varicosities, and was used to determine patient eligibility. The site clinician used a set of reference photographs (2 example photographs for each score on the scale) to assist with assigning a score to the appearance of the patient's visible varicose veins. (NCT01197833)
Timeframe: IPR-V3 measured at baseline and then at 8 weeks

Interventionscore (Least Squares Mean)
Endovenous Ablation, Vehicle Placebo-0.80
Endovenous Ablation, Polidocanol Injectable Foam, 0.5%-1.30
Endovenous Ablation, Polidocanol Injectable Foam 1.0%-1.11

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Absolute Change From Baseline in PA-V3 Score

"The Patient Self-assessment of Visible Varicose Veins (PA-V3) instrument is a 5-point scale used by patients to evaluate the appearance of their visible varicose veins. On this paper questionnaire, the instructions included a diagram of the medial view of a leg with the area between the ankle and the groin circled. The patient was instructed to choose 1 of 5 response options that best described the appearance of the visible varicose veins of the leg that was treated in the study. The patient was instructed not to consider the appearance of the leg outside the circled area or of any spider veins. Possible responses ranged from Not at all noticeable (a score of 0) to Extremely noticeable (a score of 4)" (NCT01197833)
Timeframe: PA-V3 measured at baseline and then at 8 weeks

Interventionscore (Least Squares Mean)
Endovenous Ablation, Vehicle Placebo-1.59
Endovenous Ablation, Polidocanol Injectable Foam, 0.5%-1.81
Endovenous Ablation, Polidocanol Injectable Foam 1.0%-1.85

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Change From Baseline at 8 Weeks Post-Treatment in IPR-V3 Score--Physician Photographic Review of Appearance

The Independent Photography Review--Visible Varicose Veins (IPR-V3) instrument is a 5-point scale used to assess the appearance of a patient's visible varicose veins. At baseline and Week 8, standardized digital photographs were taken of the medial view of the patient's target leg, from groin to ankle. An independent photography review panel, consisting of 3 trained, blinded clinicians, evaluated the appearance of the patient's visible varicose veins using the IPR-V3 instrument's 5-point scale (0-4, where 0=none and 4=very severe visible varicose veins). (NCT01231373)
Timeframe: 8 weeks

Interventionunits on a scale (Least Squares Mean)
Vehicle-0.32
Polidocanol Injectable Foam, 0.125%-1.55
Polidocanol Injectable Foam, 0.5%-1.86
Polidocanol Injectable Foam, 1.0%-1.79

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Change From Baseline to 8 Weeks in Appearance as Rated by Patient (PA-V3)

"The Patient Self-assessment of Visible Varicose Veins (PA-V3) instrument is a 5-point scale used by patients to evaluate the appearance of their visible varicose veins. On this single-item paper questionnaire, the instructions included a diagram fo the medial view of a leg with the area between the ankle and the groin circled. The patient was instructed to choose 1 of 5 response options that best described the appearance of the visible varicose veins of the leg that was treated in the study. The patient was instructed not to consider the appearance of the leg outside the circled area or of any spider veins. Possible responses ranged from Not at all noticeable (a score of 0) to Extremely noticeable (a score of 4)." (NCT01231373)
Timeframe: 8 weeks

Interventionunits on a scale (Mean)
Vehicle-0.07
Polidocanol Injectable Foam, 0.125%-0.74
Polidocanol Injectable Foam, 0.5%-0.89
Polidocanol Injectable Foam, 1.0%-0.83

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Change in Patient-Reported Symptoms of Varicose Veins (VVSymQ Score)

The 9 varicose vein symptoms were to be assessed and graded on a 6-point (i.e., 0-5) duration scale and an 11-point (i.e., 0-10) intensity scale, and the patient's level activity for that day was to be assessed and graded on the 6-point (i.e., 0-5) duration scale. The 9 varicose vein symptoms assessed using the e-diary were derived from the first question of the modified Venous Insufficiency Epidemiologic and Economic Study-Quality of Life/Symptoms (VEINES-QOL/Sym) instrument. The VVSymQ is a subset of 5 VEINES QOL/Sym items that have been determined in earlier studies to be most important to patients. The daily VVSymQ score is the sum of the duration scores for these 5 symptoms (scores range from 0 to 25). At Visit 2/baseline, Week 8, scores were calculated. (NCT01231373)
Timeframe: 8 weeks

Interventionunits on a scale (Least Squares Mean)
Vehicle-2.00
Polidocanol Injectable Foam, 0.125%-5.34
Polidocanol Injectable Foam, 0.5%-6.01
Polidocanol Injectable Foam, 1.0%-5.06

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Weight-adjusted Polidocanol Cmax (Serum)

Cmax measured and adjusted for weight (NCT01428076)
Timeframe: pharmacokinetics measured- predose, 1, 4, 5, 7, 9, 11, 14, 15, 17, 20, 25, 30 minutes post dose, 1, 2, 3, 4, 5, 6, 8 hours post dose

Interventionng/mL (Mean)
Males-polidocanol 1%584.1
Males-polidocanol 2%1188.7
Females-polidocanol 1%840.7
Females- Polidocanol 2%1189.6

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Efficacy in Treating Reticular Veins by Photographs: Mean Percent Reticular Vein Disappearance Two Months After Treatment.

Photographs were performed pretreatment and two months after the treatment, these were analyzed for efficacy in treat reticular veins by two blind analyzers objectively with measurement through the use of free software ImageJ. (NCT02054325)
Timeframe: Mean Percent of reticular vein disappearance two months after treatment

Intervention% of Reticular Veins that Disappeared (Mean)
Polidocanol With Glucose95.17
Glucose85.40

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The Safety of the Treatment: Mean Percent of Skin Hyperpigmentation Two Months After Treatment

"Skin hyperpigmentation was defined as a brownish hue stain superimposing the previous treated vein site (by visual photographic analyses). Skin hyperpigmentation was firstly evaluated according to its occurence and labeled as Yes or No. Afterwards, when there was stain in the previous treated area, a line was drawn on the stain with Image J software , and the Mean Percent of Skin Hyperpigmentation was proportionaly compared with length of vein treated, previuos mesuread (mean and SD)." (NCT02054325)
Timeframe: Two months after treatment.

InterventionPercent of Skin Hyperpigmentation (Mean)
Polidocanol With Glucose5.75
Glucose9.66

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Pain

14-day average post-treatment pain using a VAS pain score. VAS pain score is an integer-valued, interval scale variable with range from 0 to 100 representing the spectrum from no pain to pain as bad as one can imagine. (NCT02462720)
Timeframe: 14 day average (0-100)

Interventionunits on a scale (Mean)
Varithena®11.3
Radiofrequency Ablation9.5

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Patient Preference

Patient preference for RFA or Varithena® using e-diary (NCT02462720)
Timeframe: 8 weeks

InterventionParticipants (Count of Participants)
Varithena®19
Radiofrequency Ablation14

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Procedural Pain

degree of procedural pain perceived by the patient obtained immediately following the procedure using a VAS pain score. VAS pain score is an integer-valued, interval scale variable with range from 0 to 100 representing the spectrum from no pain to pain as bad as one can imagine (NCT02462720)
Timeframe: immediately following procedure

Interventionunits on a scale (Mean)
Varithena®16.4
Radiofrequency Ablation17.8

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Change From Baseline in Extent of Telangiectasias

Efficiency in promoting the disappearance of the treated telangiectasias, making the comparison between the initial measurements in centimeters and after two months, then comparing the treatment between the two treatments (NCT02657252)
Timeframe: 2 months

Interventionpercent of change negative values (Mean)
Glucose57.24
Polidocanol With Glucose76.08

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Number of Participants With Deep Venous Thrombosis (DVT)

Observe after one week of treatment occurred if clinical signs and symptoms of deep vein thrombosis (DVT) and perform duplex ultrasound for confirmation. Compare the results between the two groups to establish a security policy. (NCT02657252)
Timeframe: 1 week

InterventionParticipants (Count of Participants)
Glucose0
Polidocanol With Glucose0

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Skin Hyperpigmentation

Observed after two months of treatment the occurrence of hyperpigmentation stains in the treated areas. Measuring in centimeters those stains and compare the two treatments together. (NCT02657252)
Timeframe: 2 months

Interventionpercentage of hyperpigmentation (Median)
Glucose0.49
Polidocanol With Glucose0

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Number of Ulcer Free Days

Mean number of ulcer free days defined as days from baseline to date of recurrence (NCT03257254)
Timeframe: Baseline to 12 months

Interventiondays (Mean)
Prospective Registry Cohort240.5

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Number of Wound Closure at 12 Weeks

Total number of healed wounds at 12 weeks post treatment. Wound healing is measured measured by photograph inputted into wound measuring technology platform. (NCT03257254)
Timeframe: Baseline to 12 weeks

Interventionwounds (Number)
Prospective Registry Cohort43

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Number of Wound Recurrences

Count of wound recurrences of healed wounds. For healed wounds, VLU recurrence was collected via phone calls and subjects at follow up timelines. (NCT03257254)
Timeframe: Baseline to 12 months

Interventionwounds (Number)
Prospective Registry Cohort7

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Number of Wounds Remaining Closed at 3 Months Post-wound Closure Date

Count of wounds remaining closed at 3 months post-wound closure determined via photograph and assessed by wound measurement technology platform. (NCT03257254)
Timeframe: Baseline to 12 months

Interventionwounds (Count of Units)
Prospective Registry Cohort47

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Time to Wound Closure

Median number of days to wound closure measured weekly. Wound closure as measured by photograph inputted into wound measuring technology platform. (NCT03257254)
Timeframe: Baseline to wound closure or to 12 months, whichever occurs first

Interventiondays (Median)
Prospective Registry Cohort89

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Change From Baseline in Wound Perimeter

Mean change in wound perimeter as measured by photograph inputted into wound measuring technology platform. Larger number indicates a lower wound perimeter compared to baseline. Epithelial migration measured by change in perimeter of wound. (NCT03257254)
Timeframe: Baseline to 12 weeks and to 12 months

Interventionmm (Mean)
at 12 weeksat 12 months
Prospective Registry Cohort29.3643.64

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Change in Pain

"Mean change in pain on numeric pain rating scale (NPRS) compared to baseline at 12 months post-treatment. Minimum value is 0 and maximum value is 10. Higher scores mean a worse outcome." (NCT03257254)
Timeframe: Baseline to 12 weeks and to 12 months

Interventionscore on a scale (Mean)
at 12 weeksat 12 months
Prospective Registry Cohort-1.4-2.5

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Change in VCSS

"Mean change in Venous Clinical Severity Score (VCSS) from baseline to 12 month follow up. VCSS assesses nine common signs/symptoms of venous disease and each item is scored individually with a minimum score of 0 and maximum score of 3. The individual items are added together to assess change from baseline. Higher scores mean worst outcome." (NCT03257254)
Timeframe: Baseline to 12 weeks and to 12 months

Interventionscore on a scale (Mean)
at 12 weeksat 12 months
Prospective Registry Cohort-5.8-10.0

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Change on EQ-5D-5L Quality of Life Assessment

"Mean change on 5-level EQ-5D (EQ-5D-5L) quality of life assessment compared to baseline at 12 months post-treatment. Minimum value is 0 and maximum value is 1. Higher score mean better outcome." (NCT03257254)
Timeframe: Baseline to 12 weeks and to 12 months

Interventionscore on a scale (Mean)
at 12 weeksat 12 months
Prospective Registry Cohort0.0660.072

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