Page last updated: 2024-12-04

cyclopentolate

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

Cyclopentolate is a synthetic anticholinergic drug that is used to dilate the pupils of the eyes. It is a tertiary amine with a similar structure to atropine, but with a shorter duration of action. Cyclopentolate is typically used for eye examinations, such as to check for refractive errors (nearsightedness, farsightedness, astigmatism). It is also used to treat conditions like iritis and uveitis. The compound is synthesized by a process that begins with the reaction of tropine with cyclopentyl bromide. This reaction yields cyclopentyltropine bromide, which is then hydrolyzed with sodium hydroxide to yield cyclopentolate. It acts by blocking the action of acetylcholine at the muscarinic receptors in the iris and ciliary muscle. Cyclopentolate is studied because it is a valuable tool for ophthalmologists, but it is important to use it cautiously because it can cause adverse effects such as blurred vision, increased intraocular pressure, and photophobia. The potential for these side effects makes it crucial to understand its mechanism of action and how to use it safely. '

Cyclopentolate: A parasympatholytic anticholinergic used solely to obtain mydriasis or cycloplegia. [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

cyclopentolate : A carboxylic ester resulting from the formal condensation of (1-hydroxycyclopentyl)(phenyl)acetic acid with N,N-dimethylethanolamine. A tertiary amine antimuscarinic with actions similar to atropine, it is used as its hydrochloride salt to produce mydriasis (excessive dilation of the pupil) and cycloplegia (paralysis of the ciliary muscle of the eye) for opthalmic diagnostic procedures. It acts more quickly than atropine and has a shorter duration of action. [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 CID2905
CHEMBL ID1201338
CHEBI ID4024
SCHEMBL ID132500
MeSH IDM0005484

Synonyms (103)

Synonym
AC-15991
CHEMBL1201338
bell pentolate
i76f4shp7j ,
2-dimethylaminoethyl 2-(1-hydroxycyclopentyl)-2-phenylacetat
unii-i76f4shp7j
BRD-A77291778-003-05-5
benzeneacetic acid, .alpha.-(1-hydroxycyclopentyl)-, 2-(dimethylamino)ethyl ester
KBIO1_000610
DIVK1C_000610
SPECTRUM_000856
SPECTRUM5_000793
PRESTWICK2_001095
BSPBIO_002097
bell pentolate (tn)
D07759
cyclopentolate (inn)
BPBIO1_001288
AB00053445
C06932
512-15-2
cyclopentolate
2-(dimethylamino)ethyl 2-(1-hydroxycyclopentyl)-2-phenylacetate
alpha-(1-hydroxycyclopentyl)benzeneacetic acid 2-(dimethylamino)ethyl ester
beta-dimethylaminoethyl (1-hydroxycyclopentyl)phenylacetate
2-(dimethylamino)ethyl 1-hydroxy-alpha-phenylcyclopentaneacetate
beta-(dimethylamino)ethyl (1-hydroxycyclopentyl)phenylacetate
2-phenyl-2-(1-hydroxycyclopentyl)ethanoic acid beta-(dimethylamino)ethyl ester
(+/-)-cyclopentolate
DB00979
1-hydroxy-alpha-phenylcyclopentaneacetic acid 2-(dimethylamino)ethyl ester
einecs 208-136-4
benzeneacetic acid, alpha-(1-hydroxycyclopentyl)-, 2-(dimethylamino)ethyl ester
cyclopentolatum [inn-latin]
ciclopentolato [inn-spanish]
cyclopentolate [inn:ban]
KBIO2_006472
KBIO2_001336
KBIO3_001317
KBIOSS_001336
KBIOGR_000886
KBIO2_003904
PRESTWICK0_001095
SPECTRUM4_000303
PRESTWICK1_001095
SPECTRUM2_001122
SPBIO_003055
SPBIO_000983
SPECTRUM3_000369
NINDS_000610
PRESTWICK3_001095
IDI1_000610
BSPBIO_001170
L000802
ciclopentolato
CHEBI:4024 ,
(+-)-cyclopentolate
cyclopentolatum
2-(dimethylamino)ethyl (1-hydroxycyclopentyl)(phenyl)acetate
NCGC00018213-02
nsc_2905
bdbm82375
cas_512-15-2
AKOS015962137
cyclopentylate
cyclopentoiate
diopentolate
FT-0624265
gtpl7153
cyclopentolate [who-dd]
cyclopentolate [mi]
cyclopentolate [inn]
2-(dimethylamino)ethyl (+/-)-1-hydroxy-.alpha.-phenylcyclopentaneacetate
cyclopentolate [vandf]
SCHEMBL132500
mydrilate (salt/mix)
cyclopentaneacetic acid, 1-hydroxy-.alpha.-phenyl-, 2-(dimethylamino)ethyl ester
cyclogyl (salt/mix)
.beta.-(dimethylamino)ethyl (1-hydroxycyclopentyl)phenylacetate
1-hydroxy-.alpha.-phenylcyclopentaneacetic acid, 2-(dimethylamino)ethyl ester
SKYSRIRYMSLOIN-UHFFFAOYSA-N
2-dimethylaminoethyl 1-hydroxy-.alpha.-phenylcyclopentaneacetate
2-(dimethylamino)ethyl (1-hydroxycyclopentyl)(phenyl)acetate #
DTXSID3048528 ,
cyclo-pentolatum
STL430452
AB00053445_12
mfcd00599448
SBI-0051324.P003
cyclopentolatum; cyclogyl; cyclopentylate
BCP21334
AS-16057
Q867332
BRD-A77291778-003-15-4
tsiklopentolat;cyclogyl;dl-cyclopentolate
H10434
A913427
EN300-7359577
dtxcid4027995
s01fa04
ciclopentolato (inn-spanish)
2-(dimethylamino)ethyl (+/-)-1-hydroxy-alpha-phenylcyclopentaneacetate
cyclopentolatum (inn-latin)

Research Excerpts

Overview

Cyclopentolate is a synthetic anticholinergic drug and antagonist of the muscarine receptors. Spray is a good alternative to traditional drops, leading to equal cycloplegic efficacy but greater tolerance in children.

ExcerptReferenceRelevance
"Cyclopentolate is a drug that dilates the pupil and relaxes accommodation (cycloplegia)."( Vault changes after cyclopentolate instillation in eyes with posterior chamber phakic intraocular lens.
Fernandes, P; Garcia-Medina, JJ; Gargallo-Martinez, B; Gonzalez-Meijome, JM; Gutierrez-Ortega, R; Rubio-Velazquez, E; Villa-Collar, C, 2020
)
1.6
"Cyclopentolate is a synthetic anticholinergic drug and antagonist of the muscarine receptors."( [Cyclopentolate as a cycloplegic drug in determination of refractive error].
Bolinovska, S; Popović, J,
)
1.76
"Cyclopentolate spray is a good alternative to traditional drops, leading to equal cycloplegic efficacy but greater tolerance in children and easier administration by the nursing staff."( [Comparative study of cyclopentolate drops versus spray in cycloplegia in children].
Ajdnik, S; Chafai, A; Cordonnier, M; Lejeune, L, 2006
)
2.09
"Cyclopentolate is a synthetic anti-cholinergic agent widely used in ophthalmology clinics. "( Acute progressive midbrain hemorrhage after topical ocular cyclopentolate administration.
Altinors, N; Calisaneller, T; Ozdemir, O; Sonmez, E,
)
1.82
"100 Cyclopentolate is an important short-acting cycloplegic and mydriatic preparation."( [Diagnostic and therapeutic use of cyclopentolate cycloplegia].
Quéré, MA, 1976
)
1.01

Effects

Cyclopentolate has been widely used as a cycloplegic and mydriatic agent for over 30 years.

ExcerptReferenceRelevance
"Cyclopentolate has been used occasionaly in diagnostic purposes: defining ocular refraction and in ophthalmoscopy."( [Cyclopentolate as a cycloplegic drug in determination of refractive error].
Bolinovska, S; Popović, J,
)
1.76
"Cyclopentolate has been widely used as a cycloplegic and mydriatic agent for over 30 years. "( Possible allergic reactions to cyclopentolate hydrochloride: case reports with literature review of uses and adverse reactions.
Hodes, DT; Jones, LW, 1991
)
2.01

Toxicity

Atropine has a side effect incidence rate 7 times higher than the incidence rate of cyclopentolate. Preterm infants undergoing Retinopathy of Prematurity Eye Exams (ROPEE) may experience adverse events.

ExcerptReferenceRelevance
"Cycloplegics are very safe and useful medications."( Avoiding adverse effects of cycloplegics in infants and children.
Gray, LG, 1979
)
0.26
" The usefulness and toxic reactions of this very valuable drug are discussed."( Systemic toxicity of cyclopentolate hydrochloride in adults following topical ocular instillation.
Awan, KJ, 1976
)
0.57
" The ocular drugs causing serious adverse ocular or systemic side effects in children include glaucoma medications, corticosteroids, phenylephrine, and the anticholinergic cycloplegics."( How safe are ocular drugs in pediatrics?
Palmer, EA, 1986
)
0.27
"A drug registry was established at Southern California College of Optometry (SCCO) to study use rates and incidence of adverse side effects of the nine pharmaceutical agents in the California optometry law."( Use of diagnostic pharmaceutical agents and incidence of adverse effects.
Applebaum, M; Jaanus, SD, 1983
)
0.27
"Preterm infants undergoing Retinopathy of Prematurity Eye Exams (ROPEE) may experience adverse events, possibly from systemic absorption of cyclopentolate."( Systemic Absorption of Cyclopentolate and Adverse Events After Retinopathy of Prematurity Exams.
Erickson, SW; Hall, RW; Hendrickson, H; Lowery, S; Mitchell, A; Yates, C, 2016
)
0.95
" Relationships between drug levels and adverse events were assessed."( Systemic Absorption of Cyclopentolate and Adverse Events After Retinopathy of Prematurity Exams.
Erickson, SW; Hall, RW; Hendrickson, H; Lowery, S; Mitchell, A; Yates, C, 2016
)
0.74
" There is a need to predict infants at risk for high blood levels of cyclopentolate in order to prevent or treat adverse events after ROPEE."( Systemic Absorption of Cyclopentolate and Adverse Events After Retinopathy of Prematurity Exams.
Erickson, SW; Hall, RW; Hendrickson, H; Lowery, S; Mitchell, A; Yates, C, 2016
)
0.98
"Uveitis due to brimonidine is a rare adverse effect, but it must be known."( Hypertensive acute granulomatous anterior uveitis as a side effect of topical brimonidine.
Arciniegas-Perasso, CA; Clemente-Tomás, R; Duch-Samper, AM; García-Ibor, F; Hervás-Hernandis, JM; Ruiz-Del Río, N, 2018
)
0.48
"Atropine has a side effect incidence rate 7 times higher than the incidence rate of cyclopentolate."( Incidence of side effects of topical atropine sulfate and cyclopentolate hydrochloride for cycloplegia in Japanese children: a multicenter study.
Fujikado, T; Hayashi, T; Kimura, A; Miki, A; Nishina, S; Sato, M; Sugasawa, J; Utsumi, T; Wakayama, A, 2018
)
0.95

Compound-Compound Interactions

Repeated administration of cyclopentolate alone or combined with phenylephrine induce a significant mydriasis for at least 48 h after the last administration in normal horses' eyes. Do not affect STT-1, IOP, digestive function, and HR.

ExcerptReferenceRelevance
" An examiner masked to drug combination and time used digital analysis to calculate pupil diameter for each photograph."( Comparison of two drug combinations for dilating dark irides.
Anderson, HA; Bertrand, KC; Fern, KD; Hu, YS; Manny, RE, 2010
)
0.36
" The combination with topical phenylephrine did not have any additional effect on mydriasis compare with the cyclopentolate alone."( Effect of topical cyclopentolate alone or combined with phenylephrine in healthy horses.
Bessonnat, A; Vanore, M, 2021
)
1.17
"Repeated administration of cyclopentolate alone or combined with phenylephrine induce a significant mydriasis for at least 48 h after the last administration in normal horses' eyes, and do not affect STT-1, IOP, digestive function, and HR."( Effect of topical cyclopentolate alone or combined with phenylephrine in healthy horses.
Bessonnat, A; Vanore, M, 2021
)
1.25

Dosage Studied

A small amount of cyclopentolate drops could induce convulsions in young children after only minutes to less than an hour. A larger dosage of atropine over the span of several hours could cause this rare and unpredictable complication.

ExcerptRelevanceReference
" The above agents, used individually for a total dosage of three drops in each eye did not provide adequate dilation for a thorough funduscopic examination."( Systemic response to mydriatic eyedrops in neonates: mydriatics in neonates.
Caputo, AR; Schnitzer, RE,
)
0.13
" Drug potency was obtained from log dose-response curves."( Factors determining the potency of mydriatic drugs in man.
Smith, SA, 1976
)
0.26
" This case demonstrates the uncommon, though serious, atropine-like side effect of cyclopentolate eyedrops (Cyclogyl, Alcon) in usual dosage in a brain damaged child without an epileptic focus."( Seizures associated with 1% cyclopentolate eyedrops.
Brown, J; Fitzgerald, DA; Hanson, RM; Kilham, HA; Martin, F; West, C, 1990
)
0.8
" Adverse effects are often related to dosage or other factors."( Mydriatic and cycloplegic drugs: a review of ocular and systemic complications.
Doughty, CB; Rengstorff, RH, 1982
)
0.26
"To determine the optimal dosage of cyclopentolate for adequate cycloplegia with minimal side effects."( Optimal dosage of cyclopentolate 1% for complete cycloplegia: a randomized clinical trial.
Bagheri, A; Givrad, S; Reza Mohebbi, M; Yazdani, S,
)
0.74
"To find the optimal dosage of cyclopentolate 1% for cycloplegic refraction in hypermetropes with brown irides, we investigated the difference in cycloplegic auto-refractions obtained after one, two, and three instillations in the same patient."( Optimal dosage of cyclopentolate 1% for cycloplegic refraction in hypermetropes with brown irides.
Mohan, K; Sharma, A,
)
0.75
" This case demonstrates the uncommon, although serious, atropine-like adverse effect of cyclopentolate eyedrops in usual dosage in child."( Inability to walk, disequilibrium, incoherent speech, disorientation following the instillation of 1% cyclopentolate eyedrops: case report.
Derinoz, O; Er, A, 2012
)
0.82
"A small amount of cyclopentolate drops could induce convulsions in young children after only minutes to less than an hour, while a larger dosage of atropine over the span of several hours could cause this rare and unpredictable complication."( Epileptic seizures induced by cycloplegic eye drops.
Goldchmit, M; Mezer, E; Nucci, P; Wygnanski-Jaffe, T, 2014
)
0.74
" These agents are rarely absorbed to systemic circulation and in some cases result with serious side effects like skin rash, tachycardia, feeding intolerance, discomfort, apnea, gastric dilatation and ileus, despite different treatment models and dosage reducing strategies."( Fatal necrotising enterocolitis due to mydriatic eye drops.
Demet, T; Mehmet, Y; Murat, S; Nilgun, K; Ozge, KA; Ozgun, U; Zafer, D, 2014
)
0.4
"The EtOH dose-response curve was not altered by pretreatment with pBBG or by transgenic overexpression of Glo1."( Glyoxalase 1 (GLO1) Inhibition or Genetic Overexpression Does Not Alter Ethanol's Locomotor Effects: Implications for GLO1 as a Therapeutic Target in Alcohol Use Disorders.
Barkley-Levenson, AM; Lagarda, FA; Palmer, AA, 2018
)
0.48
" However, neither manipulation altered the dose-response curve for EtOH's locomotor effects, whereas muscimol appeared to enhance the locomotor sedative effects of EtOH."( Glyoxalase 1 (GLO1) Inhibition or Genetic Overexpression Does Not Alter Ethanol's Locomotor Effects: Implications for GLO1 as a Therapeutic Target in Alcohol Use Disorders.
Barkley-Levenson, AM; Lagarda, FA; Palmer, AA, 2018
)
0.48
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (4)

RoleDescription
mydriatic agentAgent that dilates the pupil. Used in eye diseases and to facilitate eye examination. It may be either a sympathomimetic or parasympatholytic. The latter cause cycloplegia or paralysis of accommodation at high doses and may precipitate glaucoma.
parasympatholyticAny cholinergic antagonist that inhibits the actions of the parasympathetic nervous system. The major group of drugs used therapeutically for this purpose is the muscarinic antagonists.
muscarinic antagonistA drug that binds to but does not activate muscarinic cholinergic receptors, thereby blocking the actions of endogenous acetylcholine or exogenous agonists.
diagnostic agentA substance administered to aid diagnosis of a disease.
[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 (3)

ClassDescription
carboxylic esterAn ester of a carboxylic acid, R(1)C(=O)OR(2), where R(1) = H or organyl and R(2) = organyl.
tertiary amino compoundA compound formally derived from ammonia by replacing three hydrogen atoms by organyl groups.
tertiary alcoholA tertiary alcohol is a compound in which a hydroxy group, -OH, is attached to a saturated carbon atom which has three other carbon atoms attached to it.
[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]

Bioassays (15)

Assay IDTitleYearJournalArticle
AID625282Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) score for cirrhosis2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID625286Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) score for hepatitis2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID625288Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) score for jaundice2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID625281Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) score for cholelithiasis2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID625289Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) score for liver disease2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID625292Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) combined score2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID625285Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) score for hepatic necrosis2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID625283Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) score for elevated liver function tests2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID625291Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) score for liver function tests abnormal2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID625290Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) score for liver fatty2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID625280Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) score for cholecystitis2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID625284Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) score for hepatic failure2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID625287Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) score for hepatomegaly2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID625279Drug Induced Liver Injury Prediction System (DILIps) training set; hepatic side effect (HepSE) score for bilirubinemia2011PLoS computational biology, Dec, Volume: 7, Issue:12
Translating clinical findings into knowledge in drug safety evaluation--drug induced liver injury prediction system (DILIps).
AID1159607Screen for inhibitors of RMI FANCM (MM2) intereaction2016Journal of biomolecular screening, Jul, Volume: 21, Issue:6
A High-Throughput Screening Strategy to Identify Protein-Protein Interaction Inhibitors That Block the Fanconi Anemia DNA Repair Pathway.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (471)

TimeframeStudies, This Drug (%)All Drugs %
pre-1990100 (21.23)18.7374
1990's95 (20.17)18.2507
2000's98 (20.81)29.6817
2010's132 (28.03)24.3611
2020's46 (9.77)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 81.38

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 Index81.38 (24.57)
Research Supply Index6.43 (2.92)
Research Growth Index4.66 (4.65)
Search Engine Demand Index145.19 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (81.38)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials90 (16.95%)5.53%
Reviews12 (2.26%)6.00%
Case Studies124 (23.35%)4.05%
Observational5 (0.94%)0.25%
Other300 (56.50%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Clinical Trials (15)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Preoperative Cataract Pupillary Dilation: Inpatient vs Outpatient [NCT01169688]50 participants (Actual)Interventional2007-12-31Completed
Nepafenac Versus Ketorolac Eye Drops in Prevention of Intraoperative Miosis During Cataract Surgery [NCT03851172]Phase 275 participants (Anticipated)Interventional2019-03-01Not yet recruiting
Combined Subconjunctival Atropine and Intracameral Epinephrine Injection for Pupil Dilation in Phacoemulsification Under Peribulbar Anesthesia. [NCT03638726]Phase 440 participants (Anticipated)Interventional2018-09-28Recruiting
Methodes of Meausring Refraction in Children Under General Anesthesia [NCT02459600]Early Phase 120 participants (Anticipated)Interventional2015-05-31Recruiting
Screening for 3-D Visual Disorders in Preschool Children, VISION Study [NCT05204069]95 participants (Actual)Interventional2021-01-01Completed
The Effect of Mydriatics on Posterior Synechia After Combined Surgery of Pars Plana Vitrectomy, Phacoemulsification, and Intraocular Lens Implantation [NCT05614622]60 participants (Actual)Interventional2020-11-10Completed
A New More Efficient Cycloplegia Scheme [NCT02177539]Phase 430 participants (Anticipated)Interventional2014-05-31Recruiting
A Randomized Controlled Trial to Determine the Lowest Effective Dose for Adequate Mydriasis in Premature Infants [NCT01054027]15 participants (Actual)Interventional2007-03-31Completed
Swiss PACK-CXL (Photoactivated Chromophore for Infectious Keratitis Cross-linking) Multicenter Trial for the Treatment of Infectious Keratitis [NCT02717871]Phase 335 participants (Actual)Interventional2016-03-31Completed
Does Undercorrection of Myopia Retard Myopia Progression Among Kindergarten [NCT00348166]Phase 1180 participants (Anticipated)Interventional2005-12-31Withdrawn(stopped due to Stringent eligibility criterion caused difficulties in recruiting patients.)
Changes in Vital Signs and Pupil Diameter Related to Pharmacologic Mydriasis in Premature Infants: A Randomized Double Blind Clinical Study [NCT04838665]Phase 460 participants (Actual)Interventional2011-09-30Completed
Tropicamide Versus Cyclopentolate Objective Refraction in Pediatric Population [NCT05442801]Phase 455 participants (Actual)Interventional2022-03-01Completed
Tropicamide Versus Cyclopentolate for Cycloplegic Refraction in Pediatric Patients With Esotropia: A Randomized Clinical Trial [NCT06077682]Phase 4100 participants (Anticipated)Interventional2023-09-01Recruiting
Optimal Method for Mydriasis in Cataract Surgery [NCT02909140]3 participants (Actual)Interventional2016-09-30Terminated(stopped due to insufficient patient recruitment)
Evaluation of a Preoperative Pharmacological Protocol for Mydriasis in Femtosecond Laser-assisted Cataract Surgery [NCT03375996]60 participants (Anticipated)Observational2018-06-01Recruiting
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

TrialOutcome
NCT02909140 (9) [back to overview]Cumulative Energy Dispersed for Each Arm
NCT02909140 (9) [back to overview]Mean Time Taken to Perform Phacoemulsification
NCT02909140 (9) [back to overview]Mean Time Taken to Perform Phacoemulsification in Each Arm
NCT02909140 (9) [back to overview]Percentage of Patients in Each Arm That Required Another Mydriatic Agent
NCT02909140 (9) [back to overview]Percentage of Patients in Each Arm That Required Use of an Iris Expansion Device During the Procedure
NCT02909140 (9) [back to overview]Pupil Size (mm) Immediately After Nuclear Disassembly
NCT02909140 (9) [back to overview]Pupil Size Immediately Prior to Capsulorrhexis
NCT02909140 (9) [back to overview]Pupil Size Immediately Prior to Intraocular Lens (IOL) Insertion
NCT02909140 (9) [back to overview]Pupil Size Upon Completion of Surgery

Cumulative Energy Dispersed for Each Arm

The amount of energy needed to break up the cataractous lens (NCT02909140)
Timeframe: During cataract surgery

InterventionPercent-seconds (Number)
Intracameral Mydriasis6.6

[back to top]

Mean Time Taken to Perform Phacoemulsification

(NCT02909140)
Timeframe: During cataract surgery

Interventionseconds (Number)
Intracameral Mydriasis76

[back to top]

Mean Time Taken to Perform Phacoemulsification in Each Arm

(NCT02909140)
Timeframe: intraoperative

Interventionseconds (Number)
Intracameral Mydriasis76

[back to top]

Percentage of Patients in Each Arm That Required Another Mydriatic Agent

(NCT02909140)
Timeframe: intraoperative

Interventionpercent of participants (Number)
Intracameral Mydriasis0

[back to top]

Percentage of Patients in Each Arm That Required Use of an Iris Expansion Device During the Procedure

(NCT02909140)
Timeframe: intraoperative

Interventionpercent (Number)
Intracameral Mydriasis50

[back to top]

Pupil Size (mm) Immediately After Nuclear Disassembly

Pupil size immediately after breaking up of cataractous lens (NCT02909140)
Timeframe: Immediately after nuclear disassembly step of cataract surgery

Interventionmm (Number)
Intracameral Mydriasis8

[back to top]

Pupil Size Immediately Prior to Capsulorrhexis

Pupil size immediately prior to the capsulorrhexis step of cataract surgery. This will be recorded by digital photography and measured by a researcher who is masked to the intervention. (NCT02909140)
Timeframe: Immediately prior to the capsulorrhexis step of cataract surgery

Interventionmm (Number)
Intracameral Mydriasis8

[back to top]

Pupil Size Immediately Prior to Intraocular Lens (IOL) Insertion

Pupil size after insertion of IOL lens (NCT02909140)
Timeframe: Immediately prior to IOL insertion step of cataract surgery

Interventionmm (Number)
Intracameral Mydriasis8

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Pupil Size Upon Completion of Surgery

(NCT02909140)
Timeframe: intraoperative

Interventionmm (Number)
Intracameral Mydriasis7

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