prednisone has been researched along with Ache in 212 studies
Prednisone: A synthetic anti-inflammatory glucocorticoid derived from CORTISONE. It is biologically inert and converted to PREDNISOLONE in the liver.
prednisone : A synthetic glucocorticoid drug that is particularly effective as an immunosuppressant, and affects virtually all of the immune system. Prednisone is a prodrug that is converted by the liver into prednisolone (a beta-hydroxy group instead of the oxo group at position 11), which is the active drug and also a steroid.
Excerpt | Relevance | Reference |
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"Treatment with abiraterone acetate and prednisone (compared with treatment with prednisone only) for metastatic castration-resistant prostate cancer increased survival in all patients in the study regardless of pain, prostate-specific antigen levels at the start of treatment, and Gleason score at primary diagnosis." | 9.27 | The Phase 3 COU-AA-302 Study of Abiraterone Acetate Plus Prednisone in Men with Chemotherapy-naïve Metastatic Castration-resistant Prostate Cancer: Stratified Analysis Based on Pain, Prostate-specific Antigen, and Gleason Score. ( Brookman-May, SD; Carles, J; Diels, J; Gschwend, JE; Miller, K; Van Poppel, H, 2018) |
"To assess the efficacy and safety of low-dose prednisone chronotherapy using a new modified-release (MR) formulation for the treatment of rheumatoid arthritis (RA)." | 9.17 | Low-dose prednisone chronotherapy for rheumatoid arthritis: a randomised clinical trial (CAPRA-2). ( Alten, RE; Boers, M; Buttgereit, F; Kirwan, J; Mehta, D; Romer, U; Saag, KG; Supronik, J; Szechinski, J; Szombati, I; Witte, S, 2013) |
"For several decades, the treatment of elderly patients with multiple myeloma (MM) has consisted of melphalan and prednisone (MP)." | 9.14 | Phase III study of the value of thalidomide added to melphalan plus prednisone in elderly patients with newly diagnosed multiple myeloma: the HOVON 49 Study. ( Ammerlaan, R; Lokhorst, H; Schaafsma, M; Sinnige, H; Sonneveld, P; Termorshuizen, F; van der Griend, R; van Marwijk Kooy, M; Wijermans, P; Wittebol, S; Zweegman, S, 2010) |
"Palliation of bone pain can be achieved in men with androgen-independent prostate cancer treated with docetaxel and estramustine (DE) or mitoxantrone and prednisone (MP)." | 9.12 | Quality of life and pain in advanced stage prostate cancer: results of a Southwest Oncology Group randomized trial comparing docetaxel and estramustine to mitoxantrone and prednisone. ( Ankerst, DP; Berry, DL; Burch, PA; Crawford, ED; Hussain, MH; Jiang, CS; Jones, S; Lara, PN; Moinpour, CM; Petrylak, DP; Taplin, ME; Vinson, LV, 2006) |
"To determine if short-acting oral therapy with prednisone was more effective than placebo in alleviating the suffering from acute pharyngitis in adults in a general practice setting." | 9.11 | Adjuvant prednisone therapy in pharyngitis: a randomised controlled trial from general practice. ( Bregman, J; Furst, AL; Kiderman, A; Yaphe, J; Zemel, T, 2005) |
"Men with HRPC, bone metastases, and bone pain were randomly assigned to receive clodronate 1,500 mg administered intravenously (IV) or placebo every 3 weeks, in combination with mitoxantrone 12 mg/m2 IV every 3 weeks and prednisone 5 mg orally bid." | 9.10 | Randomized, double-blind, controlled trial of mitoxantrone/prednisone and clodronate versus mitoxantrone/prednisone and placebo in patients with hormone-refractory prostate cancer and pain. ( Chi, K; Ding, K; Elliott, C; Ernst, DS; Moore, MJ; Parulekar, W; Reyno, L; Tannock, IF; Venner, PM; Winquist, EW, 2003) |
"In relatively healthy persons older than 50 years of age who have localized herpes zoster, combined acyclovir and prednisone therapy can improve quality of life." | 9.08 | Acyclovir with and without prednisone for the treatment of herpes zoster. A randomized, placebo-controlled trial. The National Institute of Allergy and Infectious Diseases Collaborative Antiviral Study Group. ( Gnann, JW; Hayden, F; Mertz, GJ; Pappas, PG; Schleupner, CJ; Soong, SJ; Tyring, S; Weiss, H; Whitley, RJ; Wolf, J, 1996) |
"In a Nordic multi-centre trial, 583 previously untreated multiple myeloma patients were randomized to receive melphalan-prednisone or melphalan-prednisone+ interferon alpha-2b at a dose of 5 million units subcutaneously, 3 d/week." | 9.08 | Effect of interferon on the health-related quality of life of multiple myeloma patients: results of a Nordic randomized trial comparing melphalan-prednisone to melphalan-prednisone + alpha-interferon. The Nordic Myeloma Study Group. ( Hjorth, M; Kaasa, S; Westin, J; Wisløff, F, 1996) |
"To determine the long-term efficacy and safety of low-dose methotrexate (MTX) in rheumatoid arthritis (RA)." | 9.07 | Long-term prospective study of methotrexate in the treatment of rheumatoid arthritis. 84-month update. ( Coblyn, JS; Falchuk, KR; Fraser, PA; Holdsworth, DE; Maier, AL; Weinblatt, ME; Weissman, BN, 1992) |
"Prednisone, 5 mg taken each morning, was added to other drugs in 18 patients with rheumatoid arthritis." | 9.05 | Low dose prednisone therapy in rheumatoid arthritis: a double blind study. ( Emkey, RD; Harris, ED; Newberg, A; Nichols, JE, 1983) |
"Patients treated with paclitaxel in the gynecologic oncology program of the Cleveland Clinic Foundation who developed arthralgias/myalgias which were uncontrolled through the use of nonsteroidal anti-inflammatory medications received low-dose oral prednisone (10 mg B." | 7.70 | Use of low-dose oral prednisone to prevent paclitaxel-induced arthralgias and myalgias. ( Belinson, J; Kennedy, A; Kulp, B; Markman, M; Peterson, G; Webster, K, 1999) |
"The eosinophilia-myalgia syndrome associated with the use of oral preparations of the amino acid L-tryptophan was recognized in late 1989." | 7.68 | Eosinophilia-myalgia syndrome associated with L-tryptophan use. ( Gertner, E; Glickstein, SL; Hathaway, DE; Roelofs, RI; Schlesinger, PA; Schned, ES; Smith, SA, 1990) |
"We describe the spectrum of clinical and histologic abnormalities of 11 women with L-tryptophan induced eosinophilia-myalgia syndrome." | 7.68 | L-tryptophan induced eosinophilia-myalgia syndrome. ( Albanese, JM; Chartash, EK; Coffey, EL; Farmer, PM; Furie, RA; Given, WP; Kaplan, MH; Susin, M; Vishnubhakat, SM, 1990) |
"We examined retrospectively the use of hydroxychloroquine in 9 patients with childhood dermatomyositis (DM)." | 7.67 | Adjunctive use of hydroxychloroquine in childhood dermatomyositis. ( Lindsley, CB; Olson, NY, 1989) |
"33 patients with advanced refractory multiple myeloma received a combination of vincristine, cyclophosphamide, carmustine, melphalan and steroids (M-2 protocol)." | 7.67 | M-2 protocol for melphalan-resistant and relapsing multiple myeloma. ( Cavo, M; Galieni, P; Gobbi, M; Tassi, C; Tura, S, 1988) |
"Thirty-seven men with symptomatic bone metastases from prostate cancer that had progressed following earlier treatment with estrogens and/or orchidectomy were treated with low-dose prednisone (7." | 7.67 | Treatment of metastatic prostatic cancer with low-dose prednisone: evaluation of pain and quality of life as pragmatic indices of response. ( Gospodarowicz, M; Meakin, W; Panzarella, T; Rider, W; Stewart, L; Tannock, I, 1989) |
"Abiraterone plus prednisone delays patient-reported pain progression and HRQoL deterioration in chemotherapy-naive patients with metastatic castration-resistant prostate cancer." | 6.27 | Abiraterone acetate plus prednisone versus prednisone alone in chemotherapy-naive men with metastatic castration-resistant prostate cancer: patient-reported outcome results of a randomised phase 3 trial. ( Autio, K; Basch, E; Cleeland, C; Fizazi, K; Griffin, T; Hao, Y; Kheoh, T; Li, S; Logothetis, CJ; Mainwaring, PN; Meyers, ML; Molina, A; Mulders, P; Rathkopf, D; Ryan, CJ; Shore, N; Smith, MR, 2013) |
"In these prespecified exploratory analyses, there was no significant difference in pain or HRQOL when olaparib was added to abiraterone." | 5.51 | Patient-reported outcomes with olaparib plus abiraterone versus placebo plus abiraterone for metastatic castration-resistant prostate cancer: a randomised, double-blind, phase 2 trial. ( Alekseev, B; Burgents, J; Chiuri, VE; Clarke, NW; Degboe, A; Fléchon, A; Gresty, C; Jassem, J; Jones, R; Kang, J; Kocak, I; Redfern, C; Saad, F; Sala, N; Thiery-Vuillemin, A; Wiechno, P, 2022) |
"In type I Gaucher's disease, episodes of severe disabling bone pain, the so called bone crises, may be resistant to all analgesics, including narcotics." | 5.29 | Effective treatment of painful bone crises in type I gaucher's disease with high dose prednisolone. ( Cohen, IJ; Katz, K; Kornreich, L; Mekhmandarov, S; Zaizov, R, 1996) |
"Treatment with abiraterone acetate and prednisone (compared with treatment with prednisone only) for metastatic castration-resistant prostate cancer increased survival in all patients in the study regardless of pain, prostate-specific antigen levels at the start of treatment, and Gleason score at primary diagnosis." | 5.27 | The Phase 3 COU-AA-302 Study of Abiraterone Acetate Plus Prednisone in Men with Chemotherapy-naïve Metastatic Castration-resistant Prostate Cancer: Stratified Analysis Based on Pain, Prostate-specific Antigen, and Gleason Score. ( Brookman-May, SD; Carles, J; Diels, J; Gschwend, JE; Miller, K; Van Poppel, H, 2018) |
"Our study confirmed that pamidronate, prednisone, and guideline-recommended anticonvulsants were effective for reducing pain intensity for CPSP." | 5.22 | Pharmacotherapies for Central Post-Stroke Pain: A Systematic Review and Network Meta-Analysis. ( Bo, Z; Gangfeng, G; Jian, W; Jian, Y; Ke, H; Maoxia, L; Xiaojing, L; Xiaolan, L; Yan, L; Yang, F; Zhao, C, 2022) |
"To assess the efficacy and safety of low-dose prednisone chronotherapy using a new modified-release (MR) formulation for the treatment of rheumatoid arthritis (RA)." | 5.17 | Low-dose prednisone chronotherapy for rheumatoid arthritis: a randomised clinical trial (CAPRA-2). ( Alten, RE; Boers, M; Buttgereit, F; Kirwan, J; Mehta, D; Romer, U; Saag, KG; Supronik, J; Szechinski, J; Szombati, I; Witte, S, 2013) |
"For several decades, the treatment of elderly patients with multiple myeloma (MM) has consisted of melphalan and prednisone (MP)." | 5.14 | Phase III study of the value of thalidomide added to melphalan plus prednisone in elderly patients with newly diagnosed multiple myeloma: the HOVON 49 Study. ( Ammerlaan, R; Lokhorst, H; Schaafsma, M; Sinnige, H; Sonneveld, P; Termorshuizen, F; van der Griend, R; van Marwijk Kooy, M; Wijermans, P; Wittebol, S; Zweegman, S, 2010) |
"To investigate the use of docetaxel 75 mg/m(2) intravenously every 3 weeks plus prednisone 5 mg orally twice daily in men with metastatic hormone-refractory prostate cancer (HRPC) progressing after first-line mitoxantrone/prednisone (MP), the primary outcome being progression-free survival with prostatic-specific antigen (PSA) and pain response, toxicity and quality of life (QoL) also assessed." | 5.13 | The Canadian Uro-Oncology Group multicentre phase II study of docetaxel administered every 3 weeks with prednisone in men with metastatic hormone-refractory prostate cancer progressing after mitoxantrone/prednisone. ( Cheng, T; Ernst, S; Karakiewicz, P; North, S; Perrotte, P; Ruether, D; Saad, F; Winquist, E, 2008) |
"Palliation of bone pain can be achieved in men with androgen-independent prostate cancer treated with docetaxel and estramustine (DE) or mitoxantrone and prednisone (MP)." | 5.12 | Quality of life and pain in advanced stage prostate cancer: results of a Southwest Oncology Group randomized trial comparing docetaxel and estramustine to mitoxantrone and prednisone. ( Ankerst, DP; Berry, DL; Burch, PA; Crawford, ED; Hussain, MH; Jiang, CS; Jones, S; Lara, PN; Moinpour, CM; Petrylak, DP; Taplin, ME; Vinson, LV, 2006) |
"This study clearly showed the efficacy of a short course of oral prednisone (3 days), versus a placebo, in the treatment of the functional signs of acute maxillary rhinosinusitis with severe pain in adults in addition to an appropriate antibiotic treatment." | 5.11 | [Treatment of functional signs of acute maxillary rhinosinusitis in adults. Efficacy and tolerance of administration of oral prednisone for 3 days]. ( Bordure, P; Coriat, F; Deslandes, B; Desmonts-Gohler, C; Dubreuil, C; Gehanno, P; Gilain, L; Jankowski, R; Klossek, JM; Serrano, E; Stoll, D, 2004) |
" Adult patients (>21 years old) with early RA (symptom duration <1 year) and severe joint pain under maximal dose of nonsteroidal anti-inflammatory drugs (NSAIDS) were started on low-dose prednisone (10 mg/day)." | 5.11 | Bone mineral density in patients with early rheumatoid arthritis treated with corticosteroids. ( Habib, GS; Haj, S, 2005) |
"To determine if short-acting oral therapy with prednisone was more effective than placebo in alleviating the suffering from acute pharyngitis in adults in a general practice setting." | 5.11 | Adjuvant prednisone therapy in pharyngitis: a randomised controlled trial from general practice. ( Bregman, J; Furst, AL; Kiderman, A; Yaphe, J; Zemel, T, 2005) |
"Men with HRPC, bone metastases, and bone pain were randomly assigned to receive clodronate 1,500 mg administered intravenously (IV) or placebo every 3 weeks, in combination with mitoxantrone 12 mg/m2 IV every 3 weeks and prednisone 5 mg orally bid." | 5.10 | Randomized, double-blind, controlled trial of mitoxantrone/prednisone and clodronate versus mitoxantrone/prednisone and placebo in patients with hormone-refractory prostate cancer and pain. ( Chi, K; Ding, K; Elliott, C; Ernst, DS; Moore, MJ; Parulekar, W; Reyno, L; Tannock, IF; Venner, PM; Winquist, EW, 2003) |
"In relatively healthy persons older than 50 years of age who have localized herpes zoster, combined acyclovir and prednisone therapy can improve quality of life." | 5.08 | Acyclovir with and without prednisone for the treatment of herpes zoster. A randomized, placebo-controlled trial. The National Institute of Allergy and Infectious Diseases Collaborative Antiviral Study Group. ( Gnann, JW; Hayden, F; Mertz, GJ; Pappas, PG; Schleupner, CJ; Soong, SJ; Tyring, S; Weiss, H; Whitley, RJ; Wolf, J, 1996) |
"Measurement of health-related quality of life was integrated into a randomized trial (NMSG 4/90) comparing melphalan/prednisone to melphalan/prednisone + interferon alpha-2b in newly diagnosed multiple myeloma." | 5.08 | Health-related quality of life assessed before and during chemotherapy predicts for survival in multiple myeloma. Nordic Myeloma Study Group. ( Hjorth, M; Wisløff, F, 1997) |
"In a Nordic multi-centre trial, 583 previously untreated multiple myeloma patients were randomized to receive melphalan-prednisone or melphalan-prednisone+ interferon alpha-2b at a dose of 5 million units subcutaneously, 3 d/week." | 5.08 | Effect of interferon on the health-related quality of life of multiple myeloma patients: results of a Nordic randomized trial comparing melphalan-prednisone to melphalan-prednisone + alpha-interferon. The Nordic Myeloma Study Group. ( Hjorth, M; Kaasa, S; Westin, J; Wisløff, F, 1996) |
"We randomized 161 hormone-refractory patients with pain to receive mitoxantrone plus prednisone or prednisone alone (10 mg daily)." | 5.08 | Chemotherapy with mitoxantrone plus prednisone or prednisone alone for symptomatic hormone-resistant prostate cancer: a Canadian randomized trial with palliative end points. ( Armitage, GR; Coppin, CM; Ernst, DS; Moore, MJ; Murphy, KC; Neville, AJ; Osoba, D; Stockler, MR; Tannock, IF; Venner, PM; Wilson, JJ, 1996) |
"To determine the long-term efficacy and safety of low-dose methotrexate (MTX) in rheumatoid arthritis (RA)." | 5.07 | Long-term prospective study of methotrexate in the treatment of rheumatoid arthritis. 84-month update. ( Coblyn, JS; Falchuk, KR; Fraser, PA; Holdsworth, DE; Maier, AL; Weinblatt, ME; Weissman, BN, 1992) |
"Prednisone, 5 mg taken each morning, was added to other drugs in 18 patients with rheumatoid arthritis." | 5.05 | Low dose prednisone therapy in rheumatoid arthritis: a double blind study. ( Emkey, RD; Harris, ED; Newberg, A; Nichols, JE, 1983) |
"A 14-day, single-blind trial of prednisone, aspirin, and placebo was carried out in 128 patients suffering from rheumatoid arthritis, using subjective criteria only (severity of pain daily on a pain chart and assessment of the drug for effectiveness)." | 5.04 | Method for assessing therapeutic potential of anti-inflammatory antirheumatic drugs in rheumatoid arthritis. ( Anderson, J; Buchanan, WW; Lee, P; Webb, J, 1973) |
" As a result, mitoxantrone plus prednisone has been demonstrated to be a useful palliative therapy that provides improvements in pain and quality of life for approximately 40% of those treated." | 4.81 | Treatment of hormone refractory prostate cancer. ( Knox, JJ; Moore, MJ, 2001) |
" The evaluated palliative treatments were pain medication only, chemotherapy consisting of mitoxantrone and prednisone, and single- and multifraction radiotherapy (RT)." | 3.72 | Radiotherapy is a cost-effective palliative treatment for patients with bone metastasis from prostate cancer. ( Konski, A, 2004) |
"Patients treated with paclitaxel in the gynecologic oncology program of the Cleveland Clinic Foundation who developed arthralgias/myalgias which were uncontrolled through the use of nonsteroidal anti-inflammatory medications received low-dose oral prednisone (10 mg B." | 3.70 | Use of low-dose oral prednisone to prevent paclitaxel-induced arthralgias and myalgias. ( Belinson, J; Kennedy, A; Kulp, B; Markman, M; Peterson, G; Webster, K, 1999) |
"We describe the spectrum of clinical and histologic abnormalities of 11 women with L-tryptophan induced eosinophilia-myalgia syndrome." | 3.68 | L-tryptophan induced eosinophilia-myalgia syndrome. ( Albanese, JM; Chartash, EK; Coffey, EL; Farmer, PM; Furie, RA; Given, WP; Kaplan, MH; Susin, M; Vishnubhakat, SM, 1990) |
"The eosinophilia-myalgia syndrome associated with the use of oral preparations of the amino acid L-tryptophan was recognized in late 1989." | 3.68 | Eosinophilia-myalgia syndrome associated with L-tryptophan use. ( Gertner, E; Glickstein, SL; Hathaway, DE; Roelofs, RI; Schlesinger, PA; Schned, ES; Smith, SA, 1990) |
"We examined retrospectively the use of hydroxychloroquine in 9 patients with childhood dermatomyositis (DM)." | 3.67 | Adjunctive use of hydroxychloroquine in childhood dermatomyositis. ( Lindsley, CB; Olson, NY, 1989) |
"Thirty-seven men with symptomatic bone metastases from prostate cancer that had progressed following earlier treatment with estrogens and/or orchidectomy were treated with low-dose prednisone (7." | 3.67 | Treatment of metastatic prostatic cancer with low-dose prednisone: evaluation of pain and quality of life as pragmatic indices of response. ( Gospodarowicz, M; Meakin, W; Panzarella, T; Rider, W; Stewart, L; Tannock, I, 1989) |
"33 patients with advanced refractory multiple myeloma received a combination of vincristine, cyclophosphamide, carmustine, melphalan and steroids (M-2 protocol)." | 3.67 | M-2 protocol for melphalan-resistant and relapsing multiple myeloma. ( Cavo, M; Galieni, P; Gobbi, M; Tassi, C; Tura, S, 1988) |
"Facial swelling, pain, and trismus are the most common postoperative sequelae after mandibular third molar (M3M) surgery." | 3.30 | Three-dimensional facial swelling evaluation of pre-operative single-dose of prednisone in third molar surgery: a split-mouth randomized controlled trial. ( Antonelli, A; Barone, S; Bennardo, F; Giudice, A, 2023) |
"The average treatment levels of pain did not differ, hence, the average mediated effect of treatment on GHRQL was zero." | 2.74 | Chemotherapeutic impact on pain and global health-related quality of life in hormone-refractory prostate cancer: Dynamically Modified Outcomes (DYNAMO) analysis of a randomized controlled trial. ( Donaldson, GW; Moinpour, CM; Nakamura, Y, 2009) |
"Acute neuritis and persistent pain are the most significant clinical manifestations of herpes zoster and are end points for clinical trials therapy." | 2.69 | Herpes zoster: risk categories for persistent pain. ( Gnann, JW; Soong, SJ; Weiss, HL; Whitley, RJ, 1999) |
"The prednisone therapy was differentiated by improvement from that of a placebo by six of the nine parameters evaluated." | 2.67 | Endocrine control of inflammation: rheumatoid arthritis double-blind, crossover clinical trial. ( Fiechtner, JJ; Johnson, LK; Miller, DR; Rice, JR; Stenberg, VI, 1992) |
"Pain is historically considered a cardinal sign of acute inflammation and a predominant symptom of IOIS." | 2.46 | Idiopathic orbital inflammatory syndrome without pain: a case report. ( Boothe, KH; Eckermann, DR; Musick, AN; Slagle, AM; Slagle, WS, 2010) |
"Fever, arthritis and skin rash was constant." | 2.41 | [Adult Still's disease: study of a series of 11 cases]. ( Ben Maïz, H; Ben Taarit, C; Turki, S, 2002) |
"Persistent pain is the most debilitating sequela and it occurs in at least 15% of individuals over 50 years of age." | 2.40 | Therapeutic approaches to the management of herpes zoster. ( Gnann, JW; Whitley, RJ, 1999) |
"The neurologic manifestations of coronavirus disease 2019 (COVID-19) are wide-ranging, including various cranial neuropathies, beyond anosmia and dysgeusia, the exact neuropathological mechanism of which are yet unknown." | 1.62 | Stridor Due to Cranial Nerve X Palsy Progressing to Polyneuropathy in a Teenager With COVID-19. ( Chelius, D; Dean, A; Marri, K; Said, A, 2021) |
"A 50% improvement of the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) or a final BASDAI score of <4 according to disease activity at baseline was chosen as the primary outcome parameter after MR prednisone." | 1.43 | Low-dose modified-release prednisone in axial spondyloarthritis: 3-month efficacy and tolerability. ( Bandinelli, F; Barreto Santiago, M; Marcassa, C; Matucci Cerinic, M; Nacci, F; Pimenta da Fonseca, E; Scazzariello, F, 2016) |
"A treatment with prednisone was introduced, and the patient's condition significantly improved." | 1.42 | [Neuralgic amyotrophy--a case report]. ( Banach, M; Miller, M, 2015) |
"Eosinophilic fasciitis (EF) is a rare connective tissue disorder characterized by symmetrical sclerodermatous skin changes primarily affecting the extremities and histologically, by thickening of the fascia with chronic inflammatory infiltrate containing eosinophils." | 1.34 | Eosinophilic fasciitis in a 57-year-old Japanese-American woman. ( Ambrocio, DU; Uramoto, K, 2007) |
"Pain is a common problem in both adults and children with Guillain-Barré Syndrome (GBS)." | 1.32 | [Contribution of corticosteroid to the treatment of pain in the acute phase of Guillain-Barré syndrome]. ( Boukhris, S; Kabore, R; Lacoste, M; Mabrouk, T; Magy, L; Vallat, JM, 2004) |
"Orbital emphysema is a common complication of orbital wall fractures (50% of blow-out fractures)." | 1.32 | [Emergency treatment of post-traumatic orbital emphysema: a case report]. ( Benharbit, M; Karim, A; Lazreq, M; Mohcine, Z, 2003) |
"Subacute thyroiditis (SAT), or granulomatous thyroiditis, is an inflammatory thyroid condition associated with pain and systemic symptoms." | 1.32 | Clinical features and outcome of subacute thyroiditis in an incidence cohort: Olmsted County, Minnesota, study. ( Aniszewski, JP; Atkinson, EJ; Fatourechi, GZ; Fatourechi, V; Jacobsen, SJ, 2003) |
"Patients with chronic immune thrombocytopenic purpura (ITP) who are unresponsive to corticosteroids require splenectomy, but if this fails, treatment is difficult." | 1.31 | Cyclosporin A for the treatment of patients with chronic idiopathic thrombocytopenic purpura refractory to corticosteroids or splenectomy. ( Kappers-Klunne, MC; van't Veer, MB, 2001) |
"Lymphadenitis at the right side of his neck preceded the symptoms." | 1.30 | Painful Horner syndrome due to arteritis of the internal carotid artery. ( Bollen, AE; de Jager, AE; Krikke, AP, 1998) |
"Three patients with Sjogren's syndrome are presented in whom frequent tonic/dystonic spasms of the limbs developed during the course of the illness." | 1.30 | Painful tonic/dystonic spasms in Sjogren's syndrome. ( Jabbari, B; Salardini, A, 1999) |
"When pain was asymmetric, the SSR amplitude was higher in the arm with greater pain." | 1.29 | The sympathetic skin response in the shoulder-hand syndrome complicating tetraplegia. ( Aisen, ML; Aisen, PS; Stallman, J, 1995) |
"In type I Gaucher's disease, episodes of severe disabling bone pain, the so called bone crises, may be resistant to all analgesics, including narcotics." | 1.29 | Effective treatment of painful bone crises in type I gaucher's disease with high dose prednisolone. ( Cohen, IJ; Katz, K; Kornreich, L; Mekhmandarov, S; Zaizov, R, 1996) |
"Two boys with acute lymphocytic leukemia (ALL) who presented with muscle pain, shortly after receiving induction chemotherapy, were evaluated." | 1.29 | Pyomyositis during induction chemotherapy for acute lymphocytic leukemia. ( Corden, TE; Morgan, ER, 1996) |
"Pain is not usually considered a symptom of chronic relapsing demyelinating polyneuropathy." | 1.29 | Upper limb pain in chronic demyelinating polyneuropathy: electrophysiological correlates. ( Brunet, DG; Zochodne, DW, 1994) |
"Findings at necropsy included necrotizing arteritis with fibrinoid necrosis, periarteritis, thrombosis, and intimal proliferation that most frequently affected small- to medium-sized vessels in the cervical spinal cord, mediastinum, and heart." | 1.28 | Systemic necrotizing vasculitis in nine young beagles. ( Davis, EL; Felsburg, PJ; Glickman, LT; Scott-Moncrieff, JC; Snyder, PW, 1992) |
"A patient with primary Hodgkin's disease of the lung is described." | 1.27 | Primary Hodgkin's disease of the lung. Case report and review of the literature. ( Czembirek, H; Homan, R; Lechner, K; Moritz, H; Neumann, E; Resch, F, 1983) |
"The pains were resistant to various analgesics." | 1.27 | Bone lesions in hairy cell leukemia. A case report and response of bone pains to steroids. ( Arkel, YS; Berman, E; Lake-Lewin, D; Savopoulos, AA, 1984) |
"Progressive diaphyseal dysplasia is characterized clinically by crippling leg pain, fatigue, headache, poor appetite, muscle weakness, and waddling gait." | 1.27 | Progressive diaphyseal dysplasia: evaluation of corticosteroid therapy. ( Alon, U; Berant, M; Kaftori, JK; Naveh, Y, 1985) |
"Aseptic necrosis of the wrist in systemic lupus erythematosus (SLE) is not rare." | 1.26 | Aseptic necrosis presenting as wrist pain in SLE. ( Abeles, M; Houghton, AN; Rothfield, NF; Urman, JD, 1977) |
"Prednisone therapy was associated with complete clearing of all clinical and laboratory abnormalities." | 1.26 | Hepatitis-associated lipid storage myopathy. ( Alperin, J; Dodson, RF; Patten, BM; Shabot, JM, 1977) |
"Pain and ophthalmoplegia were both relatively late manifestations preceded for several weeks by progressive involvement of the optic nerve." | 1.26 | Unusual course of painful ophthalmoplegia. Report of a case. ( Andersson, BI, 1980) |
"Criteria for the diagnosis of multiple myeloma and differential diagnostic considerations are presented." | 1.26 | [Prognosis and therapy of multiple myeloma]. ( Sonntag, RW, 1978) |
"A review of 869 cases of multiple myeloma seen at the Mayo Clinic from 1960 through 1971 revealed that 98% of patients were 40 years of age or older and that 61% of them were males." | 1.25 | Multiple myeloma: review of 869 cases. ( Kyle, RA, 1975) |
" Dose-response studies indicate that bradykinin is more potent than serotonin or histamine in respect of wealing." | 1.25 | Responses of skin blood vessels to bradykinin, histamine and 5-hydroxytryptamine. ( Greaves, M; Shuster, S, 1967) |
"Carotid system arteritis may be easily overlooked in everyday practice." | 1.25 | Carotid system arteritis: an overlooked and misdiagnosed syndrome. ( Gaston, GW; Troiano, MF, 1975) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 86 (40.57) | 18.7374 |
1990's | 36 (16.98) | 18.2507 |
2000's | 47 (22.17) | 29.6817 |
2010's | 31 (14.62) | 24.3611 |
2020's | 12 (5.66) | 2.80 |
Authors | Studies |
---|---|
Zareie, F | 1 |
Ghalebandi, S | 1 |
Askari, K | 1 |
Mousavi, Z | 1 |
Haghparast, A | 1 |
Dean, A | 1 |
Said, A | 1 |
Marri, K | 1 |
Chelius, D | 1 |
Procopio, G | 1 |
Chiuri, VE | 2 |
Giordano, M | 1 |
Alitto, AR | 1 |
Maisano, R | 1 |
Bordonaro, R | 1 |
Cinieri, S | 1 |
Rossetti, S | 1 |
De Placido, S | 1 |
Airoldi, M | 1 |
Galli, L | 1 |
Gasparro, D | 1 |
Ludovico, GM | 1 |
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Sala-Gonzalez, N | 1 |
Méndez-Vidal, MJ | 1 |
Pinto, A | 1 |
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Cuevas Sanz, JM | 1 |
Muñoz Del Toro, JR | 1 |
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García García-Porrero, Á | 1 |
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Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
A Randomised, Double-Blind, Placebo-Controlled, Multicentre Phase II Study to Compare the Efficacy, Safety and Tolerability of Olaparib Versus Placebo When Given in Addition to Abiraterone Treatment in Patients With Metastatic Castrate-Resistant Prostate [NCT01972217] | Phase 2 | 158 participants (Actual) | Interventional | 2014-04-01 | Completed | ||
A Phase 3, Randomized, Double-blind, Placebo-Controlled Study of Abiraterone Acetate (CB7630) Plus Prednisone in Asymptomatic or Mildly Symptomatic Patients With Metastatic Castration-Resistant Prostate Cancer[NCT00887198] | Phase 3 | 1,088 participants (Actual) | Interventional | 2009-04-28 | Completed | ||
Docetaxel and Estramustine Versus Mitoxantrone and Prednisone for Advanced, Hormone Refractory Prostate Cancer[NCT00004001] | Phase 3 | 770 participants (Actual) | Interventional | 1999-10-31 | Completed | ||
A Pilot Study on the Efficacy of Daratumumab in Multiple Myeloma (MM) Patients in >VGPR/MRD-positive by Next Generation Flow[NCT03992170] | Phase 2 | 50 participants (Anticipated) | Interventional | 2018-12-31 | Recruiting | ||
A Prospective, Observational Study, to Evaluate the Maintenance With Bortezomib Plus Daratumumab (V-Dara) After Induction With Bortezomib, Melphalan, Prednisone Plus Daratumumab (VMP-Dara) in Newly Diagnosed Multiple Myeloma (MM) Patients Non-eligible for[NCT05218603] | 100 participants (Anticipated) | Observational | 2021-11-30 | Recruiting | |||
A Randomized Multi-Center, Double-Blind, Placebo-Controlled Study of a New Modified-Release Tablet Formulation of Prednisone (Lodotra®) in Patients With Rheumatoid Arthritis[NCT00650078] | Phase 3 | 350 participants (Actual) | Interventional | 2008-03-31 | Completed | ||
Efficiency and Safety Study of Short-term Prednisone to Treat Moderate and Severe Subacute Thyroiditis[NCT01837433] | Phase 4 | 40 participants (Actual) | Interventional | 2013-03-31 | Completed | ||
Randomized Placebo-Controlled Trial of Mitoxantrone/Prednisone and Clodronate Versus Mitoxantrone/Prednisone Alone in Patients With Hormone Refractory Metastatic Prostate Cancer and Pain[NCT00003232] | Phase 3 | 227 participants (Actual) | Interventional | 1997-11-24 | Completed | ||
LINFOTARGAM: First-line Treatment With Dose-dense Chemotherapy Plus Rituximab (R-CHOP/14) and Highly Active Antiretroviral Therapy (HAART) in Patients With Diffuse Large B Cell Lymphoma (DLBCL) and Infection With the Human Immunodeficiency Virus (HIV)[NCT00466258] | Phase 4 | 50 participants (Anticipated) | Interventional | 2006-10-31 | Completed | ||
A Trial of Prednisone and Acetaminophen Versus Acetaminophen Alone in Minimizing Flu-like Symptoms From Pegylated Interferon Beta-1a[NCT03424733] | Phase 4 | 50 participants (Anticipated) | Interventional | 2017-09-25 | Recruiting | ||
Use of a Single Dose of Oral Prednisone in the Treatment of Cellulitis[NCT01671423] | 42 participants (Actual) | Interventional | 2012-08-31 | Completed | |||
Randomized, Placebo Controlled, Phase II Trial, on the Effect of an Oral Supplement,TK3 (Tryptophan and Thiamine) on the Quality of Life and Chemotherapy Tolerance in Cancer Patients With Advanced Disease.[NCT03341286] | Phase 2 | 140 participants (Anticipated) | Interventional | 2017-11-30 | Not yet recruiting | ||
Phase II Multicenter Study Evaluating the Efficacy of Carboplatin-Etoposide Combination in Hormone-resistant Prostate Cancers With Neuroendocrine Differentiation.[NCT00973882] | Phase 2 | 60 participants (Actual) | Interventional | 2005-04-30 | Completed | ||
A Phase II Study of Oral Calcitriol in Combination With Ketoconazole in Castration Resistant Prostate Cancer, Progressing Despite Primary ADT and Abiraterone[NCT03261336] | Phase 2 | 1 participants (Actual) | Interventional | 2017-01-06 | Terminated (stopped due to can not meet enrollment) | ||
Patient Self-administration of Cortisol for Cortisol-responding Disorders in Men and Women Over the Age of 17, Demonstration of Double-blind Trial Results[NCT03558971] | Phase 4 | 2,430 participants (Actual) | Interventional | 2000-01-01 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
"DLTs were assessed by a Safety Review Committee (SRC) after a minimum of 3 patients had received at least 14 days of treatment in Part A.~A DLT was defined as any toxicity which was not a recognised AE of abiraterone or prednisolone, and was not attributable to the disease or disease-related processes under investigation, which occurred during a minimum period of 14 days treatment and which included: 1. haematological toxicity CTCAE v4.0 Grade 4 or higher present for more than 4 days (except anaemia); 2. non-haematological toxicity CTCAE v4.0 Grade 3 or higher including infection, corrected QT interval prolongation; 3. any other toxicity that was greater than that at baseline, was clinically significant and/or unacceptable, did not respond to supportive care, resulted in a disruption of dosing schedule of 7 days or more, or was judged to be a DLT by the SRC.~A DLT excluded alopecia and isolated laboratory changes of any grade without clinical sequelae or clinical significance." (NCT01972217)
Timeframe: From Day 1 for Cohort 1 and from Day 4 for Cohort 2 up to 14 days treatment with olaparib + abiraterone for 3 patients.
Intervention | Patients (Number) |
---|---|
Part A Cohort 1: Olaparib 200 mg + Abiraterone | 2 |
Part A Cohort 2: Olaparib 300 mg + Abiraterone | 4 |
"The median best percentage change from baseline in CTC levels was determined to assess the anti-tumour activity of olaparib when given in combination with abiraterone, compared with placebo given in addition to abiraterone.~The best percentage change was defined as the biggest CTC level reduction compared with baseline or smallest increase in the absence of a decrease." (NCT01972217)
Timeframe: From baseline, then every 4 weeks up to Week 24, and then every 12 weeks.
Intervention | Percentage change in CTC level (Median) |
---|---|
Part B: Olaparib + Abiraterone | -1.0 |
Part B: Placebo + Abiraterone | -1.0 |
"The best percentage change from baseline in PSA levels was determined to assess the anti-tumour activity of olaparib when given in addition to abiraterone, compared with placebo given in addition to abiraterone.~The best percentage change was defined as the biggest reduction in PSA level compared with baseline or smallest increase in the absence of a decrease." (NCT01972217)
Timeframe: From baseline, then every 4 weeks up to Week 52, and then every 12 weeks.
Intervention | Percentage change in PSA level (Median) |
---|---|
Part B: Olaparib + Abiraterone | -54.16 |
Part B: Placebo + Abiraterone | -49.85 |
"OS was determined to assess the efficacy of olaparib when given in addition to abiraterone, compared with placebo given in addition to abiraterone.~OS was performed at the time of the analysis of rPFS, and the median OS, calculated using the Kaplan-Meier technique, is presented." (NCT01972217)
Timeframe: From baseline, every 12 weeks up to Week 72, then every 24 weeks up to 24 months.
Intervention | Months (Median) |
---|---|
Part B: Olaparib + Abiraterone | 22.7 |
Part B: Placebo + Abiraterone | 20.9 |
"The efficacy of olaparib when given in combination with abiraterone was assessed by rPFS, defined as the time from randomisation to disease progression using Response Evaluation Criteria in Solid Tumours (RECIST) version 1.1 (for soft tissue disease) and Prostate Cancer Working Group 2 (PCWG-2) (for bone disease) criteria, or death.~Progression using RECIST 1.1 criteria was defined as at least 20% increase from baseline in the sum of diameters of target lesions, progression of existing non-target lesions, or the appearance of at least 1 new lesion.~Progression using PCWG-2 criteria was determined if 2 or more new metastatic bone lesions were observed (with a total of at least 4 new lesions since baseline assessment if observed at the 12 week scan, or persistence of or increase in number of lesions if observed after the 12 week scan as determined by a confirmatory scan at least 6 weeks later or at next scheduled visit)." (NCT01972217)
Timeframe: From baseline, every 12 weeks up to Week 72, then every 24 weeks up to 24 months.
Intervention | Months (Median) |
---|---|
Part B: Olaparib + Abiraterone | 13.8 |
Part B: Placebo + Abiraterone | 8.2 |
The efficacy of olaparib when given in combination with abiraterone was assessed by PFS2, defined by local standard clinical practice and included objective radiological progression by RECIST 1.1 (soft tissue), symptomatic progression, rise in PSA level or death in the absence of overall progression. (NCT01972217)
Timeframe: From randomisation until analysis cut-off date (up to approximately 3 years).
Intervention | Months (Median) |
---|---|
Part B: Olaparib + Abiraterone | 23.3 |
Part B: Placebo + Abiraterone | 18.5 |
"The overall radiological ORR was calculated to assess the anti-tumour activity of olaparib in combination with abiraterone, compared with placebo in combination with abiraterone.~The best overall ORR was defined as the percentage of patients with at least 1 visit response of complete response (CR) or partial response (PR) in soft tissue disease assessed by RECIST 1.1 and also bone scan status of non-progressive disease or non-evaluable for their bone scans assessed by PCWG-2.~CR: Disappearance of all target lesions. Reduction of pathological lymph nodes to <10 millimetres.~PR: At least a 30% decrease in the sum of diameters of target lesions from baseline.~The percentage of patients with a response is presented." (NCT01972217)
Timeframe: From baseline, then every 4 weeks up to Week 52, and then every 12 weeks.
Intervention | Percentage of patients (Number) |
---|---|
Part B: Olaparib + Abiraterone | 27.3 |
Part B: Placebo + Abiraterone | 31.6 |
"The efficacy of olaparib when given in combination with abiraterone was assessed by rPFS, defined as the time from randomisation to disease progression using RECIST version 1.1 (for soft tissue disease) and PCWG-2 (for bone disease) criteria, or death.~Progression using RECIST 1.1 criteria was defined as at least 20% increase from baseline in the sum of diameters of target lesions, progression of existing non-target lesions, or the appearance of at least 1 new lesion.~Progression using PCWG-2 criteria was determined if 2 or more new metastatic bone lesions were observed (with a total of at least 4 new lesions since baseline assessment if observed at the 12 week scan, or persistence of or increase in number of lesions if observed after the 12 week scan as determined by a confirmatory scan at least 6 weeks later or at next scheduled visit).~The percentage of patients with progression events is presented overall and according to RECIST 1.1 and/or PCWG-2 criteria, or death." (NCT01972217)
Timeframe: From baseline, every 12 weeks up to Week 72, then every 24 weeks up to 24 months.
Intervention | Percentage of patients (Number) |
---|---|
Part B: Olaparib + Abiraterone | 64.8 |
Part B: Placebo + Abiraterone | 76.1 |
"The TFST and TSST were determined to assess the anti-tumour activity of olaparib when given in combination with abiraterone, compared with placebo given in addition to abiraterone.~TFST was defined as the time from randomisation to the earlier of first subsequent anti-cancer therapy start date following study treatment discontinuation, or death.~TSST was defined as the time from randomisation to the earlier of the second subsequent anti-cancer therapy start date following study treatment discontinuation, or death." (NCT01972217)
Timeframe: From randomisation until analysis cut-off date (up to approximately 3 years).
Intervention | Months (Median) | |
---|---|---|
TFST | TSST | |
Part B: Olaparib + Abiraterone | 13.5 | 19.6 |
Part B: Placebo + Abiraterone | 9.7 | 18.0 |
"Following multiple dosing to steady state of olaparib 300 mg bid, the Cohort 2 olaparib Cmax,ss is presented for olaparib monotherapy and for olaparib given in combination with abiraterone.~Only patients with data available for analysis at each time point are presented." (NCT01972217)
Timeframe: PK sampling for Cohort 2 Group 1 was between Days 3 and 7 for olaparib, and Days 4 and 8 for olaparib and abiraterone. PK sampling for Cohort 2 Group 2 was between Days 5 and 7 for abiraterone, and Days 6 and 8 for olaparib and abiraterone.
Intervention | micrograms per millilitre (mcg/mL) (Geometric Mean) |
---|---|
Olaparib + abiraterone | |
Part A Cohort 2 Group 2: Abiraterone, Olaparib + Abiraterone | 7.724 |
"Following multiple dosing to steady state of olaparib 300 mg bid, the Cohort 2 olaparib Cmax,ss is presented for olaparib monotherapy and for olaparib given in combination with abiraterone.~Only patients with data available for analysis at each time point are presented." (NCT01972217)
Timeframe: PK sampling for Cohort 2 Group 1 was between Days 3 and 7 for olaparib, and Days 4 and 8 for olaparib and abiraterone. PK sampling for Cohort 2 Group 2 was between Days 5 and 7 for abiraterone, and Days 6 and 8 for olaparib and abiraterone.
Intervention | micrograms per millilitre (mcg/mL) (Geometric Mean) | |
---|---|---|
Olaparib alone | Olaparib + abiraterone | |
Part A Cohort 2 Group 1: Olaparib, Olaparib + Abiraterone | 7.781 | 6.504 |
"Following multiple dosing to steady state of olaparib 300 mg bid, the Cohort 2 olaparib AUCss is presented for olaparib monotherapy and for olaparib given in combination with abiraterone.~Only patients with data available for analysis at each time point are presented." (NCT01972217)
Timeframe: PK sampling for Cohort 2 Group 1 was between Days 3 and 7 for olaparib, and Days 4 and 8 for olaparib and abiraterone. PK sampling for Cohort 2 Group 2 was between Days 5 and 7 for abiraterone, and Days 6 and 8 for olaparib and abiraterone.
Intervention | mcg*h/mL (Geometric Mean) |
---|---|
Olaparib + abiraterone | |
Part A Cohort 2 Group 2: Abiraterone, Olaparib + Abiraterone | 49.51 |
"Following multiple dosing to steady state of olaparib 300 mg bid, the Cohort 2 olaparib AUCss is presented for olaparib monotherapy and for olaparib given in combination with abiraterone.~Only patients with data available for analysis at each time point are presented." (NCT01972217)
Timeframe: PK sampling for Cohort 2 Group 1 was between Days 3 and 7 for olaparib, and Days 4 and 8 for olaparib and abiraterone. PK sampling for Cohort 2 Group 2 was between Days 5 and 7 for abiraterone, and Days 6 and 8 for olaparib and abiraterone.
Intervention | mcg*h/mL (Geometric Mean) | |
---|---|---|
Olaparib alone | Olaparib + abiraterone | |
Part A Cohort 2 Group 1: Olaparib, Olaparib + Abiraterone | 45.27 | 40.83 |
"Following multiple dosing to steady state of olaparib 300 mg bid, the Cohort 2 olaparib Cmin,ss is presented for olaparib monotherapy and for olaparib given in combination with abiraterone.~Only patients with data available for analysis at each time point are presented." (NCT01972217)
Timeframe: PK sampling for Cohort 2 Group 1 was between Days 3 and 7 for olaparib, and Days 4 and 8 for olaparib and abiraterone. PK sampling for Cohort 2 Group 2 was between Days 5 and 7 for abiraterone, and Days 6 and 8 for olaparib and abiraterone.
Intervention | mcg/mL (Geometric Mean) |
---|---|
Olaparib + abiraterone | |
Part A Cohort 2 Group 2: Abiraterone, Olaparib + Abiraterone | 1.279 |
"Following multiple dosing to steady state of olaparib 300 mg bid, the Cohort 2 olaparib Cmin,ss is presented for olaparib monotherapy and for olaparib given in combination with abiraterone.~Only patients with data available for analysis at each time point are presented." (NCT01972217)
Timeframe: PK sampling for Cohort 2 Group 1 was between Days 3 and 7 for olaparib, and Days 4 and 8 for olaparib and abiraterone. PK sampling for Cohort 2 Group 2 was between Days 5 and 7 for abiraterone, and Days 6 and 8 for olaparib and abiraterone.
Intervention | mcg/mL (Geometric Mean) | |
---|---|---|
Olaparib alone | Olaparib + abiraterone | |
Part A Cohort 2 Group 1: Olaparib, Olaparib + Abiraterone | 1.264 | 0.9170 |
"Following multiple dosing to steady state of olaparib 300 mg bid, the Cohort 2 olaparib tmax,ss is presented for olaparib monotherapy and for olaparib given in combination with abiraterone.~Only patients with data available for analysis at each time point are presented." (NCT01972217)
Timeframe: PK sampling for Cohort 2 Group 1 was between Days 3 and 7 for olaparib, and Days 4 and 8 for olaparib and abiraterone. PK sampling for Cohort 2 Group 2 was between Days 5 and 7 for abiraterone, and Days 6 and 8 for olaparib and abiraterone.
Intervention | Hours (h) (Median) |
---|---|
Olaparib + abiraterone | |
Part A Cohort 2 Group 2: Abiraterone, Olaparib + Abiraterone | 2.000 |
"Following multiple dosing to steady state of olaparib 300 mg bid, the Cohort 2 olaparib tmax,ss is presented for olaparib monotherapy and for olaparib given in combination with abiraterone.~Only patients with data available for analysis at each time point are presented." (NCT01972217)
Timeframe: PK sampling for Cohort 2 Group 1 was between Days 3 and 7 for olaparib, and Days 4 and 8 for olaparib and abiraterone. PK sampling for Cohort 2 Group 2 was between Days 5 and 7 for abiraterone, and Days 6 and 8 for olaparib and abiraterone.
Intervention | Hours (h) (Median) | |
---|---|---|
Olaparib alone | Olaparib + abiraterone | |
Part A Cohort 2 Group 1: Olaparib, Olaparib + Abiraterone | 2.000 | 2.080 |
"Following multiple dosing to steady state of abiraterone 1000 mg once daily, the Cohort 2 abiraterone AUCss is presented for abiraterone monotherapy and for olaparib given in combination with abiraterone.~Only patients with data available for analysis at each time point are presented." (NCT01972217)
Timeframe: PK sampling for Cohort 2 Group 1 was between Days 3 and 7 for olaparib, and Days 4 and 8 for olaparib and abiraterone. PK sampling for Cohort 2 Group 2 was between Days 5 and 7 for abiraterone, and Days 6 and 8 for olaparib and abiraterone.
Intervention | ng*h/mL (Geometric Mean) |
---|---|
Olaparib + abiraterone | |
Part A Cohort 2 Group 1: Olaparib, Olaparib + Abiraterone | 718.9 |
"Following multiple dosing to steady state of abiraterone 1000 mg once daily, the Cohort 2 abiraterone AUCss is presented for abiraterone monotherapy and for olaparib given in combination with abiraterone.~Only patients with data available for analysis at each time point are presented." (NCT01972217)
Timeframe: PK sampling for Cohort 2 Group 1 was between Days 3 and 7 for olaparib, and Days 4 and 8 for olaparib and abiraterone. PK sampling for Cohort 2 Group 2 was between Days 5 and 7 for abiraterone, and Days 6 and 8 for olaparib and abiraterone.
Intervention | ng*h/mL (Geometric Mean) | |
---|---|---|
Abiraterone alone | Olaparib + abiraterone | |
Part A Cohort 2 Group 2: Abiraterone, Olaparib + Abiraterone | 825.5 | 524.6 |
"Following multiple dosing to steady state of abiraterone 1000 mg once daily, the Cohort 2 abiraterone Cmax,ss is presented for abiraterone monotherapy and for olaparib given in combination with abiraterone.~Only patients with data available for analysis at each time point are presented." (NCT01972217)
Timeframe: PK sampling for Cohort 2 Group 1 was between Days 3 and 7 for olaparib, and Days 4 and 8 for olaparib and abiraterone. PK sampling for Cohort 2 Group 2 was between Days 5 and 7 for abiraterone, and Days 6 and 8 for olaparib and abiraterone.
Intervention | nanograms per millilitre (ng/mL) (Geometric Mean) |
---|---|
Olaparib + abiraterone | |
Part A Cohort 2 Group 1: Olaparib, Olaparib + Abiraterone | 130.7 |
"Following multiple dosing to steady state of abiraterone 1000 mg once daily, the Cohort 2 abiraterone Cmax,ss is presented for abiraterone monotherapy and for olaparib given in combination with abiraterone.~Only patients with data available for analysis at each time point are presented." (NCT01972217)
Timeframe: PK sampling for Cohort 2 Group 1 was between Days 3 and 7 for olaparib, and Days 4 and 8 for olaparib and abiraterone. PK sampling for Cohort 2 Group 2 was between Days 5 and 7 for abiraterone, and Days 6 and 8 for olaparib and abiraterone.
Intervention | nanograms per millilitre (ng/mL) (Geometric Mean) | |
---|---|---|
Abiraterone alone | Olaparib + abiraterone | |
Part A Cohort 2 Group 2: Abiraterone, Olaparib + Abiraterone | 145.8 | 86.12 |
"Following multiple dosing to steady state of abiraterone 1000 mg once daily, the Cohort 2 abiraterone Cmin,ss is presented for abiraterone monotherapy and for olaparib given in combination with abiraterone.~Only patients with data available for analysis at each time point are presented." (NCT01972217)
Timeframe: PK sampling for Cohort 2 Group 1 was between Days 3 and 7 for olaparib, and Days 4 and 8 for olaparib and abiraterone. PK sampling for Cohort 2 Group 2 was between Days 5 and 7 for abiraterone, and Days 6 and 8 for olaparib and abiraterone.
Intervention | ng/mL (Geometric Mean) |
---|---|
Olaparib + abiraterone | |
Part A Cohort 2 Group 1: Olaparib, Olaparib + Abiraterone | 7.983 |
"Following multiple dosing to steady state of abiraterone 1000 mg once daily, the Cohort 2 abiraterone Cmin,ss is presented for abiraterone monotherapy and for olaparib given in combination with abiraterone.~Only patients with data available for analysis at each time point are presented." (NCT01972217)
Timeframe: PK sampling for Cohort 2 Group 1 was between Days 3 and 7 for olaparib, and Days 4 and 8 for olaparib and abiraterone. PK sampling for Cohort 2 Group 2 was between Days 5 and 7 for abiraterone, and Days 6 and 8 for olaparib and abiraterone.
Intervention | ng/mL (Geometric Mean) | |
---|---|---|
Abiraterone alone | Olaparib + abiraterone | |
Part A Cohort 2 Group 2: Abiraterone, Olaparib + Abiraterone | 8.376 | 6.358 |
"Following multiple dosing to steady state of abiraterone 1000 mg once daily, the Cohort 2 abiraterone tmax,ss is presented for abiraterone monotherapy and for olaparib given in combination with abiraterone.~Only patients with data available for analysis at each time point are presented." (NCT01972217)
Timeframe: PK sampling for Cohort 2 Group 1 was between Days 3 and 7 for olaparib, and Days 4 and 8 for olaparib and abiraterone. PK sampling for Cohort 2 Group 2 was between Days 5 and 7 for abiraterone, and Days 6 and 8 for olaparib and abiraterone.
Intervention | Hours (Median) |
---|---|
Olaparib + abiraterone | |
Part A Cohort 2 Group 1: Olaparib, Olaparib + Abiraterone | 3.000 |
"Following multiple dosing to steady state of abiraterone 1000 mg once daily, the Cohort 2 abiraterone tmax,ss is presented for abiraterone monotherapy and for olaparib given in combination with abiraterone.~Only patients with data available for analysis at each time point are presented." (NCT01972217)
Timeframe: PK sampling for Cohort 2 Group 1 was between Days 3 and 7 for olaparib, and Days 4 and 8 for olaparib and abiraterone. PK sampling for Cohort 2 Group 2 was between Days 5 and 7 for abiraterone, and Days 6 and 8 for olaparib and abiraterone.
Intervention | Hours (Median) | |
---|---|---|
Abiraterone alone | Olaparib + abiraterone | |
Part A Cohort 2 Group 2: Abiraterone, Olaparib + Abiraterone | 2.525 | 2.500 |
"The safety and tolerability of olaparib in combination with abiraterone was assessed during Part A of the study. The percentage of patients experiencing AEs, including information on seriousness, severity, study treatment relationship and those leading to discontinuation for all doses of olaparib and for abiraterone are presented.~Severity of AEs was assessed using the National Cancer Institute (NCI) Common Terminology Criteria for Adverse events (CTCAE) v4.0. AEs were assigned to a Grade from 1 through 5 as follows:~Grade 1: Mild; Grade 2: Moderate; Grade 3: Severe or medically significant but not immediately life-threatening requiring hospitalisation; Grade 4: Life-threatening consequences; Grade 5: Death related to AE.~'c-r' = causally related 'discont' = discontinuation." (NCT01972217)
Timeframe: Cohort 1 and 2: From baseline in Part A (Day 1 for each cohort) up to 30 days following last dose of study treatment.
Intervention | Percentage of patients (Number) | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Any AE c-r to olaparib + abiraterone | Any AE c-r to olaparib only | Any AE c-r to abiraterone only | Any AE CTCAE Grade 3 or higher | Any AE CTCAE Grade 3 or higher c-r to olaparib | Any AE CTCAE Grade 3 or higher c-r to abiraterone | Any AE with outcome = death | Any serious AE (SAE) | Any SAE c-r to olaparib | Any SAE c-r to abiraterone | Any AE causing discont of olaparib | Any AE causing discont of olaparib c-r to olaparib | Any AE causing discont olaparib c-r to abiraterone | |
Part A Cohort 1: Olaparib 200 mg + Abiraterone | 66.7 | 33.3 | 0 | 66.7 | 0 | 0 | 0 | 66.7 | 0 | 0 | 0 | 0 | 0 |
Part A Cohort 2: Olaparib 300 mg + Abiraterone | 46.2 | 7.7 | 15.4 | 23.1 | 7.7 | 7.7 | 0 | 23.1 | 0 | 0 | 7.7 | 0 | 0 |
"The safety and tolerability of olaparib when given in combination with abiraterone was assessed during Part B of the study. The percentage of patients experiencing AEs, including information on seriousness, severity, study treatment relationship and those leading to discontinuation for all doses of olaparib and for abiraterone are presented.~Severity of AEs was assessed using the NCI Common Terminology CTCAE v4.0. AEs were assigned to a Grade from 1 through 5 as follows:~Grade 1: Mild; Grade 2: Moderate; Grade 3: Severe or medically significant but not immediately life-threatening requiring hospitalisation; Grade 4: Life-threatening consequences; Grade 5: Death related to AE.~'c-r' = causally related. 'discont' = discontinuation. 'ola/pla' = olaparib/placebo." (NCT01972217)
Timeframe: From first dose of study treatment following randomisation in Part B up to 30 days following last dose of study treatment (up to approximately 3 years).
Intervention | Percentage of patients (Number) | ||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Any AE c-r to ola/pla + abiraterone | Any AE c-r to ola/pla only | Any AE c-r to abiraterone only | Any AE CTCAE Grade 3 or higher | Any AE CTCAE Grade 3 or higher c-r to ola/pla | Any AE CTCAE Grade 3 or higher c-r to abiraterone | Any AE with outcome = death | Any AE with outcome = death c-r to ola/pla | Any AE with outcome = death c-r to abiraterone | Any SAE | Any SAE c-r to ola/pla | Any SAE c-r to abiraterone | Any AE causing discont of ola/pla | Any AE causing discont of treatment c-r to ola/pla | Any AE causing discont treatment c-r abiraterone | |
Part B: Olaparib + Abiraterone | 45.1 | 18.3 | 1.4 | 53.5 | 23.9 | 16.9 | 5.6 | 1.4 | 0 | 35.2 | 9.9 | 5.6 | 29.6 | 16.9 | 8.5 |
Part B: Placebo + Abiraterone | 12.7 | 9.9 | 7.0 | 28.2 | 5.6 | 1.4 | 1.4 | 0 | 0 | 19.7 | 1.4 | 0 | 9.9 | 5.6 | 1.4 |
"The percentages of patients with single visit responses and with confirmed responses are presented to assess the anti-tumour activity of olaparib when given in addition to abiraterone, compared with placebo given in addition to abiraterone.~A single visit response was defined as any post-dose visit PSA level reduced by 50% or more compared with baseline.~A confirmed response was defined as a reduction in PSA level of 50% or more on 2 consecutive occasions at least 4 weeks apart compared with baseline.~Patients may have had more than 1 single visit response or confirmed response but were counted once." (NCT01972217)
Timeframe: From baseline, then every 4 weeks up to Week 24, and then every 12 weeks.
Intervention | Percentage of patients (Number) | |
---|---|---|
Single visit response | Confirmed response | |
Part B: Olaparib + Abiraterone | 50.7 | 47.9 |
Part B: Placebo + Abiraterone | 47.9 | 42.3 |
Overall survival is defined as the time from randomization to date of death from any cause. (NCT00887198)
Timeframe: From randomization (Day 1) up to end of study (Month 60)
Intervention | Months (Median) |
---|---|
Abiraterone Acetate + Prednisone (AAP) | 34.66 |
Placebo | 30.29 |
The rPFS was defined as the time from randomization to the occurrence of one of the following: 1) a participant was considered to have progressed by bone scan if - a) the first bone scan with greater than or equal to (>=) 2 new lesions compared to baseline was observed in less than (<) 12 weeks from randomization and was confirmed by a second bone scan taken >=6 weeks later showing >=2 additional new lesions (a total of >=4 new lesions compared to baseline), b) the first bone scan with >=2 new lesions compared to baseline was observed in >=12 weeks from randomization and the new lesions were verified on the next bone scan >=6 weeks later (a total of >=2 new lesions compared to baseline); 2) progression of soft tissue lesions measured by computerized tomography (CT) or magnetic resonance imaging (MRI); 3) death from any cause. (NCT00887198)
Timeframe: From randomization (Day 1) up to first radiographic progression or cutoff date (Month 18)
Intervention | Months (Median) |
---|---|
Abiraterone Acetate + Prednisone (AAP) | NA |
Placebo | 8.28 |
The time interval from the date of randomization to the first date at which there was at least a 1 grade change (worsening) in the ECOG performance status grade. Participants who had no deterioration in ECOG performance status grade at the time of the analysis were censored at the last known date of no deterioration. ECOG is a 5-point scale, where 0=Fully active, 1=Ambulatory, carry out work of sedentary nature, 2=Ambulatory, capable of all self-care, 3=Capable of limited self-care, confined to bed or chair more than 50% of waking hours, 4=Completely disabled, no self-care, totally confined to bed or chair, 5=Dead. Participants with no assessment were censored at the date of randomization. (NCT00887198)
Timeframe: From randomization (Day 1) up to first radiographic progression or cutoff date (Month 18)
Intervention | Months (Median) |
---|---|
Abiraterone Acetate + Prednisone (AAP) | 12.29 |
Placebo | 10.87 |
The time interval from the date of randomization to the date of initiation of cytotoxic chemotherapy for prostate cancer. Participants who had no cytotoxic chemotherapy administration at the time of analysis were censored at the last known date when no cytotoxic chemotherapy was administered. Participants with no assessment were censored at the date of randomization. (NCT00887198)
Timeframe: From randomization (Day 1) up to initiation of cytotoxic chemotherapy or cutoff date (Month 18)
Intervention | Months (Median) |
---|---|
Abiraterone Acetate + Prednisone (AAP) | 25.17 |
Placebo | 16.82 |
The time interval from the date of randomization to the date of opiate use for cancer pain. Participants who have no opiate use at the time of analysis were censored at the last known date of no opiate use for cancer pain. Participants with no assessment were censored at the date of randomization. (NCT00887198)
Timeframe: From randomization (Day 1) up to first opiate use or end of study (Month 60)
Intervention | Months (Median) |
---|---|
Abiraterone Acetate + Prednisone (AAP) | 33.38 |
Placebo | 23.39 |
The time interval from the date of randomization to the date of PSA progression as defined in the protocol-specific prostate cancer Working Group 2 (PCWG2) criteria. A participant was considered to have a PSA progression if the PSA level had a 25 percent (%) or greater increase from nadir and an absolute increase of 2 nanogram/milliliter ((ng/mL) or more, which is confirmed by a second value obtained in 3 or more weeks. Participants who had no PSA progression at the time of the analysis were censored at the last known date of no PSA progression. Participants with no on-study PSA assessment or no baseline PSA assessment were censored at the date of randomization. (NCT00887198)
Timeframe: From randomization (Day 1) up to date of PSA progerssion or cutoff date (Month 18)
Intervention | Months (Median) |
---|---|
Abiraterone Acetate + Prednisone (AAP) | 11.07 |
Placebo | 5.55 |
An adverse event (AE) was any untoward medical occurrence in a participant who received study drug without regard to possibility of causal relationship. A serious adverse event (SAE) was an AE resulting in any of the following outcomes or deemed significant for any other reason: death; initial or prolonged inpatient hospitalization; life-threatening experience (immediate risk of dying); persistent or significant disability/incapacity; congenital anomaly. Treatment-emergent were events between administration of study drug and up to 30 days after last dose of study drug that were absent before treatment or that worsened relative to pre-treatment state. (NCT00887198)
Timeframe: From first dose of study drug up to 30 days after the last dose of study drug
Intervention | Participants (Number) | |
---|---|---|
With Treatment-Emergent Adverse Events | With Treatment-Emergent Serious Adverse Events | |
Abiraterone Acetate + Prednisone (AAP) | 541 | 208 |
Placebo | 524 | 148 |
Placebo to Abiraterone Acetate | 93 | 39 |
"Responders were defined as patients whose improvement from baseline to Visit 4 (Week 12) fulfilled all 3 of the following criteria:~> 20% reduction in the tender joint count (0-28)~> 20% reduction in the swollen joint count (0-28)~> 20% reduction in 3 out of the 5 following additional measures:~Patient's assessment of pain~Patient's global assessment of disease activity~Physician's global assessment of disease activity~Functional Disability Index of the Health Assessment Questionnaire~C-reactive protein or erythrocyte sedimentation rate" (NCT00650078)
Timeframe: Week 12
Intervention | participants (Number) |
---|---|
NP01 | 108 |
Placebo | 34 |
Data for the duration of morning stiffness were obtained from patient diaries. Duration of morning stiffness was the difference between the time of resolution of morning stiffness and the time of wake-up. Duration of morning stiffness is the average of the morning stiffness duration (minutes) over the last 7 days prior to visit day (including day of visit). If more than 4 assessments were missing, then the duration was set to missing. Baseline was the value recorded at Week -1 (Visit 0). (NCT00650078)
Timeframe: Week 12
Intervention | Relative Change from Baseline (%) (Median) |
---|---|
NP01 | -55.22 |
Placebo | -34.62 |
Number of times the subject needed to use pain medication between day 1 and the 48 hour follow-up (NCT01671423)
Timeframe: Assessed once during the 48 hour follow-up
Intervention | medications taken (Median) |
---|---|
Prednisone | 7 |
Placebo | 2 |
The level of pain as measured by a Visual Analog Scale(VAS) measured once at day 1 and once during the 48th hour follow-up visit. Minimum value 0, maximum value 100mm, higher scores corresponds to more pain/worse outcomes. (NCT01671423)
Timeframe: Assessed once at day 1 and then once during the 48 hour follow-up
Intervention | score on a scale (Mean) | |
---|---|---|
VAS at Day 1 | VAS at 48 hrs | |
Placebo | 56.45 | 25.91 |
Prednisone | 79.64 | 39.71 |
Descriptive analysis of observed toxicity and patient reports of tolerating experimental treatment (NCT03261336)
Timeframe: 2 years
Intervention | Participants (Count of Participants) |
---|---|
Calcitriol, Ketoconazole, Hydrocortisone | 1 |
14 reviews available for prednisone and Ache
Article | Year |
---|---|
Pharmacotherapies for Central Post-Stroke Pain: A Systematic Review and Network Meta-Analysis.
Topics: Anticonvulsants; Etanercept; Humans; Lamotrigine; Levetiracetam; Network Meta-Analysis; Pain; Pamidr | 2022 |
Abiraterone acetate plus prednisone versus prednisone alone in chemotherapy-naive men with metastatic castration-resistant prostate cancer: patient-reported outcome results of a randomised phase 3 trial.
Topics: Abiraterone Acetate; Activities of Daily Living; Androstadienes; Antineoplastic Combined Chemotherap | 2013 |
Eosinophilic cystitis: three cases, and a review over 10 years.
Topics: Adolescent; Aged; Aged, 80 and over; Anti-Inflammatory Agents; Cystitis; Diagnosis, Differential; Eo | 2014 |
Idiopathic orbital inflammatory syndrome without pain: a case report.
Topics: Aged; Conjunctival Diseases; Dacryocystitis; Diagnosis, Differential; Edema; Humans; Inflammation; M | 2010 |
[Retroperitoneal fibrosis, an unrecognized inflammatory disease. Clinical observations and review of the literature].
Topics: Aged; Anemia; Aortic Aneurysm; Female; Humans; Inflammation; Male; Middle Aged; Pain; Prednisone; Pr | 2003 |
Chronic recurrent multifocal osteomyelitis of the spine and mandible: case report and review of the literature.
Topics: Alendronate; Anti-Bacterial Agents; Anti-Inflammatory Agents, Non-Steroidal; Child, Preschool; Chron | 2004 |
Analgesic efficacy of dextropropoxyphene and dextropropoxyphene-containing combinations: a review.
Topics: Acetaminophen; Aminoacridines; Antineoplastic Combined Chemotherapy Protocols; Aspirin; Chlorambucil | 1984 |
Therapeutic approaches to the management of herpes zoster.
Topics: 2-Aminopurine; Acyclovir; Antiviral Agents; Famciclovir; Herpes Zoster; Humans; Pain; Prednisone; Pr | 1999 |
Treatment of hormone refractory prostate cancer.
Topics: Adenocarcinoma; Antineoplastic Agents, Hormonal; Antineoplastic Combined Chemotherapy Protocols; Est | 2001 |
[Adult Still's disease: study of a series of 11 cases].
Topics: Adult; Anemia; Diagnosis, Differential; Exanthema; Female; Ferritins; Fever; Humans; Incidence; Infe | 2002 |
[Primary hyperparathyroidism. An analysis of 152 patients with special references to acute life threatening complications (acute hyperparathyroidism)].
Topics: Acute Disease; Adenoma; Adolescent; Adult; Aged; Alkaline Phosphatase; Bone and Bones; Calcium; Diab | 1976 |
[Polymyositis].
Topics: Antineoplastic Agents; Child; Dermatomyositis; Enzymes; Humans; Immunosuppression Therapy; Methotrex | 1976 |
[Multiple myeloma. Biological, prognostic, and therapeutic aspects].
Topics: Antineoplastic Combined Chemotherapy Protocols; Biomarkers, Tumor; Bone Marrow Transplantation; Comb | 1990 |
[Algodystrophic syndromes].
Topics: Adult; Age Factors; Alcoholism; Diabetes Complications; Female; Humans; Hyperthyroidism; Male; Pain; | 1974 |
38 trials available for prednisone and Ache
Article | Year |
---|---|
Patient-reported outcomes with olaparib plus abiraterone versus placebo plus abiraterone for metastatic castration-resistant prostate cancer: a randomised, double-blind, phase 2 trial.
Topics: Androgen Antagonists; Androgens; Androstenes; Antineoplastic Combined Chemotherapy Protocols; Doceta | 2022 |
Three-dimensional facial swelling evaluation of pre-operative single-dose of prednisone in third molar surgery: a split-mouth randomized controlled trial.
Topics: Adult; Disease Progression; Female; Humans; Male; Molar, Third; Mouth; Pain; Prednisone; Retrospecti | 2023 |
The Phase 3 COU-AA-302 Study of Abiraterone Acetate Plus Prednisone in Men with Chemotherapy-naïve Metastatic Castration-resistant Prostate Cancer: Stratified Analysis Based on Pain, Prostate-specific Antigen, and Gleason Score.
Topics: Abiraterone Acetate; Aged; Antineoplastic Combined Chemotherapy Protocols; Double-Blind Method; Huma | 2018 |
Abiraterone acetate plus prednisone versus prednisone alone in chemotherapy-naive men with metastatic castration-resistant prostate cancer: patient-reported outcome results of a randomised phase 3 trial.
Topics: Abiraterone Acetate; Activities of Daily Living; Androstadienes; Antineoplastic Combined Chemotherap | 2013 |
Prognostic model predicting metastatic castration-resistant prostate cancer survival in men treated with second-line chemotherapy.
Topics: Aged; Alkaline Phosphatase; Antineoplastic Combined Chemotherapy Protocols; Area Under Curve; Biomar | 2013 |
Improvement Thresholds for Morning Stiffness Duration in Patients Receiving Delayed- Versus Immediate-Release Prednisone for Rheumatoid Arthritis.
Topics: Adult; Aged; Antirheumatic Agents; Arthritis, Rheumatoid; Circadian Rhythm; Delayed-Action Preparati | 2015 |
The Canadian Uro-Oncology Group multicentre phase II study of docetaxel administered every 3 weeks with prednisone in men with metastatic hormone-refractory prostate cancer progressing after mitoxantrone/prednisone.
Topics: Aged; Antineoplastic Combined Chemotherapy Protocols; Disease Progression; Docetaxel; Humans; Male; | 2008 |
Chemotherapeutic impact on pain and global health-related quality of life in hormone-refractory prostate cancer: Dynamically Modified Outcomes (DYNAMO) analysis of a randomized controlled trial.
Topics: Antineoplastic Combined Chemotherapy Protocols; Docetaxel; Estramustine; Humans; Male; Mitoxantrone; | 2009 |
Phase I/II study on docetaxel, gemcitabine and prednisone in castrate refractory metastatic prostate cancer.
Topics: Aged; Aged, 80 and over; Anti-Inflammatory Agents; Antimetabolites, Antineoplastic; Antineoplastic A | 2010 |
Phase III study of the value of thalidomide added to melphalan plus prednisone in elderly patients with newly diagnosed multiple myeloma: the HOVON 49 Study.
Topics: Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Female; Humans; Kaplan-Meie | 2010 |
Phase III study of the value of thalidomide added to melphalan plus prednisone in elderly patients with newly diagnosed multiple myeloma: the HOVON 49 Study.
Topics: Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Female; Humans; Kaplan-Meie | 2010 |
Phase III study of the value of thalidomide added to melphalan plus prednisone in elderly patients with newly diagnosed multiple myeloma: the HOVON 49 Study.
Topics: Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Female; Humans; Kaplan-Meie | 2010 |
Phase III study of the value of thalidomide added to melphalan plus prednisone in elderly patients with newly diagnosed multiple myeloma: the HOVON 49 Study.
Topics: Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Female; Humans; Kaplan-Meie | 2010 |
Low-dose prednisone chronotherapy for rheumatoid arthritis: a randomised clinical trial (CAPRA-2).
Topics: Adult; Aged; Aged, 80 and over; Anti-Inflammatory Agents; Antirheumatic Agents; Arthritis, Rheumatoi | 2013 |
Randomised phase II/III study of docetaxel with or without risedronate in patients with metastatic Castration Resistant Prostate Cancer (CRPC), the Netherlands Prostate Study (NePro).
Topics: Aged; Aged, 80 and over; Androgen Antagonists; Antineoplastic Agents, Phytogenic; Antineoplastic Com | 2012 |
Randomized, double-blind, controlled trial of mitoxantrone/prednisone and clodronate versus mitoxantrone/prednisone and placebo in patients with hormone-refractory prostate cancer and pain.
Topics: Aged; Antineoplastic Combined Chemotherapy Protocols; Bone Neoplasms; Clodronic Acid; Disease Progre | 2003 |
Open-label, randomized study of pegfilgrastim vs. daily filgrastim as an adjunct to chemotherapy in elderly patients with non-Hodgkin's lymphoma.
Topics: Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Australia; Combined Modalit | 2003 |
[Treatment of functional signs of acute maxillary rhinosinusitis in adults. Efficacy and tolerance of administration of oral prednisone for 3 days].
Topics: Acetaminophen; Administration, Oral; Adult; Analgesics, Non-Narcotic; Anti-Bacterial Agents; Anti-In | 2004 |
Corticosteroids, ibuprofen, and acetaminophen for IFNbeta-1a flu symptoms in MS: a randomized trial.
Topics: Acetaminophen; Adult; Analgesics, Non-Narcotic; Asthenia; Chills; Double-Blind Method; Drug Administ | 2004 |
Quality of life assessment in elderly patients with aggressive non-Hodgkin's Lymphoma treated with anthracycline-containing regimens. Report of a prospective study by the Intergruppo Italiano Linfomi.
Topics: Aged; Anthracyclines; Antineoplastic Combined Chemotherapy Protocols; Appetite; Bleomycin; Cyclophos | 2004 |
Bone mineral density in patients with early rheumatoid arthritis treated with corticosteroids.
Topics: Absorptiometry, Photon; Adult; Aged; Aged, 80 and over; Antirheumatic Agents; Arthritis, Rheumatoid; | 2005 |
Adjuvant prednisone therapy in pharyngitis: a randomised controlled trial from general practice.
Topics: Adolescent; Adult; Aged; Anti-Inflammatory Agents; Chemotherapy, Adjuvant; Dose-Response Relationshi | 2005 |
Quality of life and pain in advanced stage prostate cancer: results of a Southwest Oncology Group randomized trial comparing docetaxel and estramustine to mitoxantrone and prednisone.
Topics: Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Bone Neoplasms; Docetaxel; | 2006 |
Quality of life and pain in advanced stage prostate cancer: results of a Southwest Oncology Group randomized trial comparing docetaxel and estramustine to mitoxantrone and prednisone.
Topics: Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Bone Neoplasms; Docetaxel; | 2006 |
Quality of life and pain in advanced stage prostate cancer: results of a Southwest Oncology Group randomized trial comparing docetaxel and estramustine to mitoxantrone and prednisone.
Topics: Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Bone Neoplasms; Docetaxel; | 2006 |
Quality of life and pain in advanced stage prostate cancer: results of a Southwest Oncology Group randomized trial comparing docetaxel and estramustine to mitoxantrone and prednisone.
Topics: Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Bone Neoplasms; Docetaxel; | 2006 |
Prostate-specific antigen and pain surrogacy analysis in metastatic hormone-refractory prostate cancer.
Topics: Adenocarcinoma; Aged; Antineoplastic Agents, Hormonal; Antineoplastic Combined Chemotherapy Protocol | 2007 |
Treatment of hormone-refractory prostate cancer with docetaxel or mitoxantrone: relationships between prostate-specific antigen, pain, and quality of life response and survival in the TAX-327 study.
Topics: Aged; Antineoplastic Agents; Antineoplastic Agents, Hormonal; Docetaxel; Humans; Male; Mitoxantrone; | 2008 |
Analgesic efficacy of dextropropoxyphene and dextropropoxyphene-containing combinations: a review.
Topics: Acetaminophen; Aminoacridines; Antineoplastic Combined Chemotherapy Protocols; Aspirin; Chlorambucil | 1984 |
Low dose prednisone therapy in rheumatoid arthritis: a double blind study.
Topics: Adolescent; Adult; Aged; Arthritis, Rheumatoid; Clinical Trials as Topic; Double-Blind Method; Femal | 1983 |
Chemotherapy with mitoxantrone plus prednisone or prednisone alone for symptomatic hormone-resistant prostate cancer: a Canadian randomized trial with palliative end points.
Topics: Adenocarcinoma; Aged; Analgesics; Androgen Antagonists; Antineoplastic Combined Chemotherapy Protoco | 1996 |
Chemotherapy with mitoxantrone plus prednisone or prednisone alone for symptomatic hormone-resistant prostate cancer: a Canadian randomized trial with palliative end points.
Topics: Adenocarcinoma; Aged; Analgesics; Androgen Antagonists; Antineoplastic Combined Chemotherapy Protoco | 1996 |
Chemotherapy with mitoxantrone plus prednisone or prednisone alone for symptomatic hormone-resistant prostate cancer: a Canadian randomized trial with palliative end points.
Topics: Adenocarcinoma; Aged; Analgesics; Androgen Antagonists; Antineoplastic Combined Chemotherapy Protoco | 1996 |
Chemotherapy with mitoxantrone plus prednisone or prednisone alone for symptomatic hormone-resistant prostate cancer: a Canadian randomized trial with palliative end points.
Topics: Adenocarcinoma; Aged; Analgesics; Androgen Antagonists; Antineoplastic Combined Chemotherapy Protoco | 1996 |
Acyclovir with and without prednisone for the treatment of herpes zoster. A randomized, placebo-controlled trial. The National Institute of Allergy and Infectious Diseases Collaborative Antiviral Study Group.
Topics: Acyclovir; Aged; Antiviral Agents; Chronic Disease; Drug Therapy, Combination; Female; Glucocorticoi | 1996 |
Effect of interferon on the health-related quality of life of multiple myeloma patients: results of a Nordic randomized trial comparing melphalan-prednisone to melphalan-prednisone + alpha-interferon. The Nordic Myeloma Study Group.
Topics: Activities of Daily Living; Aged; Antineoplastic Combined Chemotherapy Protocols; Fatigue; Feeding a | 1996 |
Health-related quality of life assessed before and during chemotherapy predicts for survival in multiple myeloma. Nordic Myeloma Study Group.
Topics: Activities of Daily Living; Aged; Antineoplastic Combined Chemotherapy Protocols; Fatigue; Forecasti | 1997 |
Herpes zoster: risk categories for persistent pain.
Topics: Activities of Daily Living; Acyclovir; Aged; Anti-Inflammatory Agents; Antiviral Agents; Female; Her | 1999 |
Anti-tumour necrosis factor treatment with infliximab in a case of giant cell arteritis resistant to steroid and immunosuppressive drugs.
Topics: Aged; Antibodies, Monoclonal; Antirheumatic Agents; Azathioprine; Drug Resistance; Drug Therapy, Com | 2002 |
Evaluation of analgesic action and efficacy of antirheumatic drugs. Study of 10 drugs in 684 patients with rheumatoid arthritis.
Topics: Acetaminophen; Anti-Inflammatory Agents, Non-Steroidal; Arthritis, Rheumatoid; Aspirin; Clinical Tri | 1976 |
[Comparative evaluation of the therapeutic efficiency of flurbiprofene in rheumatoid polyarthritis].
Topics: Acetaminophen; Arthritis, Rheumatoid; Aspirin; Biphenyl Compounds; Chemical Phenomena; Chemistry; Cl | 1975 |
Endocrine control of inflammation: rheumatoid arthritis double-blind, crossover clinical trial.
Topics: Adult; Aged; Analysis of Variance; Arthritis, Rheumatoid; Double-Blind Method; Female; Humans; Male; | 1992 |
Long-term prospective study of methotrexate in the treatment of rheumatoid arthritis. 84-month update.
Topics: Aged; Arthritis, Rheumatoid; Biopsy; Drug Administration Schedule; Humans; Liver; Liver Cirrhosis; M | 1992 |
Method for assessing therapeutic potential of anti-inflammatory antirheumatic drugs in rheumatoid arthritis.
Topics: Anti-Inflammatory Agents; Arthritis, Rheumatoid; Aspirin; Clinical Trials as Topic; Humans; Methods; | 1973 |
Treatment of pain in hemophilia. Effect of drugs on bleeding time.
Topics: Administration, Oral; Analgesics; Aspirin; Blood Coagulation; Blood Coagulation Tests; Blood Platele | 1974 |
Proceedings: Technique for assessing the potential effectiveness of antirheumatic drugs.
Topics: Arthritis, Rheumatoid; Aspirin; Clinical Trials as Topic; Drug Evaluation; Ethics, Medical; Humans; | 1974 |
[Experience with paramethasone in sarcoidosis].
Topics: Female; Humans; Lung Diseases; Male; Middle Aged; Pain; Paramethasone; Prednisone; Psychoses, Substa | 1970 |
162 other studies available for prednisone and Ache
Article | Year |
---|---|
Orexin receptors in the CA1 region of hippocampus modulate the stress-induced antinociceptive responses in an animal model of persistent inflammatory pain.
Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Benzoxazoles; CA1 Region, Hippocampal; Cycl | 2022 |
Stridor Due to Cranial Nerve X Palsy Progressing to Polyneuropathy in a Teenager With COVID-19.
Topics: Acute Disease; Adolescent; Combined Modality Therapy; COVID-19; Deglutition Disorders; Diagnosis, Di | 2021 |
Real-world experience of abiraterone acetate plus prednisone in chemotherapy-naive patients with metastatic castration-resistant prostate cancer: long-term results of the prospective ABItude study.
Topics: Abiraterone Acetate; Aged; Antineoplastic Combined Chemotherapy Protocols; Humans; Male; Pain; Predn | 2022 |
Quality of life outcomes for patients with metastatic castration-resistant prostate cancer and pretreatment prognostic score.
Topics: Aged; Analgesics, Opioid; Antineoplastic Combined Chemotherapy Protocols; Docetaxel; Humans; Male; P | 2023 |
Recurrent diabetic myonecrosis in an African American woman with long-standing uncontrolled type 2 diabetes: a case report.
Topics: Biopsy; Black or African American; Diabetes Mellitus, Type 2; Female; Humans; Infarction; Middle Age | 2023 |
T-Cell Lymphoblastic Lymphoma Presenting as Acute Clavicular Pain.
Topics: Antineoplastic Combined Chemotherapy Protocols; Child; Daunorubicin; Humans; Pain; Precursor Cell Ly | 2019 |
Acute Kidney Injury With Massively Enlarged Noncystic Kidneys.
Topics: Acute Kidney Injury; Adolescent; Biopsy; Diagnosis, Differential; Female; Glomerular Filtration Rate | 2020 |
Tibia stress injury and the imaging appearance of stress fracture in juvenile dermatomyositis: six patients' experiences.
Topics: Adolescent; Analgesics; Antirheumatic Agents; Child; Dermatomyositis; Female; Fractures, Bone; Fract | 2021 |
Atypical Sympathetic Ophthalmia Presenting with Ocular Pain Associated with Posterior Scleral Involvement.
Topics: Adult; Choroid; Female; Fluorescein Angiography; Humans; Ophthalmia, Sympathetic; Pain; Prednisone | 2022 |
Isolated Polyarteritis Nodosa Presenting as Bilateral Testicular Swelling.
Topics: Cyclophosphamide; Debridement; Edema; Glucocorticoids; Humans; Immunosuppressive Agents; Male; Metho | 2018 |
Customizing Daily Management of Castrate-resistant Prostate Cancer: Waiting for the Next Step.
Topics: Abiraterone Acetate; Humans; Male; Neoplasm Grading; Pain; Prednisone; Prostate-Specific Antigen; Pr | 2018 |
An Unusual Cause of Leg Pain.
Topics: Aged; Biopsy; Carotid Arteries; Coronary Angiography; Coronary Artery Bypass; Coronary Stenosis; Dru | 2017 |
Extremely Painful Multifocal Acquired Predominant Axonal Sensorimotor Neuropathy of the Upper Limb.
Topics: Aged; Autoimmune Diseases of the Nervous System; Brachial Plexus Neuritis; Diagnosis, Differential; | 2018 |
Woman With Hand Pain and Swelling.
Topics: Adult; Anti-Inflammatory Agents; Calcinosis; Edema; Emergency Service, Hospital; Female; Hand; Human | 2018 |
Systemic lupus erythematosus-associated neutrophilic dermatosis manifesting as an acneiform eruption and foot pain.
Topics: Acneiform Eruptions; Antirheumatic Agents; Female; Foot; Glucocorticoids; Humans; Hydroxychloroquine | 2019 |
What Is the Optimal Dose of Predniso(lo)ne for Induction of Remission in Patients With Autoimmune Hepatitis?
Topics: Acetaminophen; Hepatitis, Autoimmune; Humans; Pain; Prednisolone; Prednisone; Remission Induction | 2020 |
Efficacy and safety of abiraterone acetate plus prednisone vs. cabazitaxel as a subsequent treatment after first-line docetaxel in metastatic castration-resistant prostate cancer: results from a prospective observational study (CAPRO).
Topics: Abiraterone Acetate; Adenocarcinoma; Age Factors; Aged; Aged, 80 and over; Anemia; Antineoplastic Ag | 2019 |
A rare cause of odynophagia and dysphagia: oesophageal lichen planus.
Topics: Adult; Anti-Inflammatory Agents; Deglutition Disorders; Esophagus; Female; Humans; Lichen Planus; Mu | 2013 |
Chronic inflammatory demyelinating polyneuropathy associated with neurosyphilis.
Topics: Anti-Bacterial Agents; Anti-Inflammatory Agents; Biopsy; Cognitive Dysfunction; Electromyography; Ex | 2015 |
Painful acute radiation thyroiditis induced by 131I treatment of Graves' disease.
Topics: Acetaminophen; Adult; Analgesics, Opioid; Anti-Inflammatory Agents; Drug Combinations; Female; Grave | 2015 |
Polymyalgia rheumatica: inflammation suppression with low dose of methylprednisolone or modified-release prednisone.
Topics: Aged; Biomarkers; Cytokines; Female; Glucocorticoids; Humans; Inflammation; Interleukin-6; Male; Met | 2015 |
Necrotizing crescentic glomerulonephritis related to sarcoidosis: a case report.
Topics: Adult; Azathioprine; Black or African American; Creatinine; Female; Foot Diseases; Glomerulonephriti | 2015 |
[Neuralgic amyotrophy--a case report].
Topics: Axons; Brachial Plexus Neuritis; Electromyography; Female; Humans; Middle Aged; Muscle, Skeletal; Pa | 2015 |
Outcome of a glucocorticoid discontinuation regimen in patients with inactive systemic sclerosis.
Topics: Adult; Aged; Disability Evaluation; Fatigue; Female; Glucocorticoids; Health Status Indicators; Huma | 2016 |
Low-dose modified-release prednisone in axial spondyloarthritis: 3-month efficacy and tolerability.
Topics: Adult; Aged; Aged, 80 and over; Anti-Inflammatory Agents; Cohort Studies; Female; Humans; Male; Midd | 2016 |
An adolescent with fever, weakness, and pain.
Topics: Adolescent; Anti-Bacterial Agents; Diagnosis, Differential; Fever; Glucocorticoids; Humans; Male; Mu | 2009 |
Vacuum-assisted biopsy and steroid therapy for granulomatous lobular mastitis: report of three cases.
Topics: Abscess; Adult; Biopsy; Combined Modality Therapy; Drainage; Female; Glucocorticoids; Granuloma; Hum | 2009 |
Terbinafine-induced acute generalized exanthematous pustulosis (AGEP) responsive to high dose intravenous corticosteroid.
Topics: Acute Generalized Exanthematous Pustulosis; Anti-Inflammatory Agents; Antifungal Agents; Clobetasol; | 2009 |
Posttraumatic psoriatic osteitis of the frontal bone successfully treated with etanercept. Report of a case.
Topics: Acetaminophen; Anti-Inflammatory Agents; Child; Craniocerebral Trauma; Drug Therapy, Combination; Et | 2010 |
Syringomyelia in the Cavalier King Charles spaniel (CKCS) dog.
Topics: Amines; Analgesics; Animals; Anti-Inflammatory Agents; Arnold-Chiari Malformation; Breeding; Cyclohe | 2010 |
Perplexing pyretic polyarthritis.
Topics: Aged; Anti-Inflammatory Agents; Arthritis; Colchicine; Diagnosis, Differential; Fever; Gout; Gout Su | 2010 |
Testicular pain followed by microscopic hematuria, a renal mass, palpable purpura, polyarthritis, and hematochezia.
Topics: Adrenal Cortex Hormones; Adult; Arthritis; Carcinoma, Renal Cell; Gastrointestinal Hemorrhage; Hemat | 2010 |
Painful genital ulcers in a 10-year old girl.
Topics: Anti-Inflammatory Agents; Child; Child Abuse, Sexual; Female; Humans; Pain; Prednisone; Pyoderma Gan | 2011 |
Clinical features and outcome of subacute thyroiditis in an incidence cohort: Olmsted County, Minnesota, study.
Topics: Adolescent; Adult; Age Factors; Aged; Aged, 80 and over; Anti-Inflammatory Agents, Non-Steroidal; Bi | 2003 |
Sarcomatoid variant of B-cell lymphoma of the uterine cervix.
Topics: Adult; Antineoplastic Combined Chemotherapy Protocols; Biopsy; Cyclophosphamide; Doxorubicin; Female | 2003 |
An unusual presentation of herpes zoster ophthalmicus: orbital myositis preceding vesicular eruption.
Topics: Acyclovir; Anti-Inflammatory Agents; Antiviral Agents; Diplopia; Drug Therapy, Combination; Female; | 2003 |
Lightning pain of tabes dorsalis treated with meticorten.
Topics: Humans; Lightning; Pain; Prednisone; Tabes Dorsalis | 1958 |
[THE ALGOGENIC RECEPTIVITY OF MUSCLE IN VARIOUS PHYSIOLOGICAL AND PATHOLOGICAL CONDITIONS. III. ACTION OF PREDNISONE, ACETYLSALICYLIC ACID AND PHENYLBUTAZONE ON THE PERCEPTION OF MUSCULAR PAIN IN THE NORMAL SUBJECT AND IN THE RHEUMATIC SUBJECT].
Topics: Arthritis; Arthritis, Rheumatoid; Aspirin; Hyperesthesia; Muscles; Myalgia; Pain; Perception; Pharma | 1963 |
ABDOMINAL PAIN IN SCHOENLEIN-HENOCH SYNDROME. ITS CORRELATION WITH SMALL BOWEL BARIUM ROENTGEN STUDY.
Topics: Abdomen; Abdominal Pain; Barium; Child; Drug Therapy; Gastrointestinal Hemorrhage; Humans; IgA Vascu | 1964 |
CHEST PAIN, DYSPNEA, AND COR PULMONALE.
Topics: Angiography; Chest Pain; Digoxin; Drug Therapy; Dyspnea; Humans; Pain; Pathology; Prednisone; Pulmon | 1965 |
ACUTE CERVICAL PAIN ASSOCIATED WITH RETROPHARYNGEAL CALCIUM DEPOSIT. A CASE REPORT.
Topics: Axis, Cervical Vertebra; Calcinosis; Calcium; Cervical Atlas; Drug Therapy; Humans; Meperidine; Neck | 1964 |
[Emergency treatment of post-traumatic orbital emphysema: a case report].
Topics: Anti-Inflammatory Agents; Cephalothin; Combined Modality Therapy; Diplopia; Drainage; Drug Therapy, | 2003 |
Spinal cord schistosomiasis: a prospective study of 63 cases emphasizing clinical and therapeutic aspects.
Topics: Adolescent; Adult; Aged; Anti-Inflammatory Agents; Antiplatyhelmintic Agents; Biopsy; Child; Child, | 2004 |
Lesser trochanteric bursitis: a rare cause of anterior hip pain.
Topics: Adult; Anti-Inflammatory Agents; Bursitis; Female; Femur; Follow-Up Studies; Hip Joint; Humans; Pain | 2004 |
Combined central retinal artery and vein occlusion from orbital inflammatory pseudotumour.
Topics: Adult; Exophthalmos; Fluorescein Angiography; Glucocorticoids; Humans; Magnetic Resonance Imaging; M | 2004 |
Painful neuropathy vasculitis in 2 patients with long-standing human immunodeficiency virus-1 infection.
Topics: Adult; Antiretroviral Therapy, Highly Active; Follow-Up Studies; HIV Infections; HIV-1; Humans; Long | 2004 |
[Contribution of corticosteroid to the treatment of pain in the acute phase of Guillain-Barré syndrome].
Topics: Glucocorticoids; Guillain-Barre Syndrome; Humans; Male; Methylprednisolone; Middle Aged; Pain; Predn | 2004 |
Radiotherapy is a cost-effective palliative treatment for patients with bone metastasis from prostate cancer.
Topics: Analgesics; Antineoplastic Agents; Bone Neoplasms; Cost-Benefit Analysis; Humans; Male; Markov Chain | 2004 |
Clinical problem-solving. Clear as mud.
Topics: Adolescent; Anti-Bacterial Agents; Blood Chemical Analysis; Creatinine; Diagnosis, Differential; Glu | 2005 |
Bilateral isolated phrenic neuropathy causing painless bilateral diaphragmatic paralysis.
Topics: Adult; Aged; Anti-Inflammatory Agents; Autoimmune Diseases of the Nervous System; Brachial Plexus Ne | 2005 |
Painful purpuric plaques on edematous hands.
Topics: Administration, Oral; Aged; Carcinosarcoma; Edema; Hand; Humans; Male; Neoplasm Metastasis; Pain; Pa | 2005 |
Retrospective review of the clinical manifestations and outcomes in Puerto Ricans with idiopathic inflammatory myopathies.
Topics: Adolescent; Adult; Anti-Inflammatory Agents; Antibodies, Antinuclear; Arthritis, Rheumatoid; Biopsy; | 2005 |
The clinical spectrum of neuralgic amyotrophy in 246 cases.
Topics: Adolescent; Adrenal Cortex Hormones; Adult; Age of Onset; Aged; Brachial Plexus; Brachial Plexus Neu | 2006 |
Depression, fatigue, and pain in systemic lupus erythematosus (SLE): relationship to the American College of Rheumatology SLE neuropsychological battery.
Topics: Adult; Cognition; Depression; Ethnicity; Fatigue; Female; Humans; Lupus Erythematosus, Systemic; Mal | 2006 |
[Fractures of vital teeth during chronic pain therapy with oxycodone].
Topics: Aged; Analgesics, Opioid; Animals; Glucocorticoids; Humans; Male; Oxycodone; Pain; Prednisone; Tooth | 2006 |
Gout, have we met before? No, not like this...
Topics: Administration, Oral; Aged; Anti-Inflammatory Agents; Arthritis, Gouty; Arthritis, Infectious; Diagn | 2006 |
Childhood steroid-responsive painful opthalmoplegia: clues to opthalmoplegic migraine.
Topics: Child; Female; Glucocorticoids; Humans; Migraine Disorders; Ophthalmoplegia; Pain; Prednisone; Remis | 2006 |
[Intravascular lymphoma causing acute abdomen].
Topics: Abdomen, Acute; Aged; Antineoplastic Combined Chemotherapy Protocols; Combined Modality Therapy; Cyc | 2007 |
Steroid treatment in children with sickle-cell disease.
Topics: Adolescent; Anemia, Sickle Cell; Arthritis; Autoimmune Diseases; Blood Transfusion; Child; Child, Pr | 2007 |
Nudulo-cystic eruption with musculoskeletal pain.
Topics: Acne Vulgaris; Adolescent; Disease Progression; Dose-Response Relationship, Drug; Drug Administratio | 2007 |
Eosinophilic fasciitis in a 57-year-old Japanese-American woman.
Topics: Anti-Inflammatory Agents, Non-Steroidal; Celecoxib; Diagnosis, Differential; Eosinophilia; Fasciitis | 2007 |
Responses of skin blood vessels to bradykinin, histamine and 5-hydroxytryptamine.
Topics: Adult; Arteries; Blood Vessels; Bradykinin; Chlorpheniramine; Female; Histamine; Humans; Hydrocortis | 1967 |
Painful ophthalmoplegia: report of a case.
Topics: Adult; Exophthalmos; Humans; Male; Ophthalmoplegia; Pain; Papilledema; Prednisone | 1967 |
Nine years of diarrhea and abdominal pain.
Topics: Aged; Crohn Disease; Diarrhea; Duodenal Diseases; Female; Humans; Joint Diseases; Pain; Prednisone; | 1983 |
Bone lesions in hairy cell leukemia. A case report and response of bone pains to steroids.
Topics: Biopsy; Bone Neoplasms; Female; Humans; Leukemia, Hairy Cell; Middle Aged; Pain; Palliative Care; Pr | 1984 |
Painful lumbosacral plexopathy with elevated erythrocyte sedimentation rate: a treatable inflammatory syndrome.
Topics: Aged; Blood Sedimentation; Cyclophosphamide; Female; Humans; Lumbosacral Plexus; Male; Middle Aged; | 1984 |
Acne fulminans with prolonged polyarthralgia.
Topics: Acne Vulgaris; Adult; HLA Antigens; Humans; Indomethacin; Joint Diseases; Male; Pain; Prednisone | 1980 |
[Painful Tolosa-Hunt ophthalmoplegia].
Topics: Adolescent; Adult; Female; Humans; Male; Middle Aged; Ophthalmoplegia; Orbit; Pain; Phlebography; Pr | 1984 |
Respiratory tract symptoms as a clue to giant cell arteritis.
Topics: Aged; Cough; Female; Giant Cell Arteritis; Glossalgia; Hoarseness; Humans; Male; Middle Aged; Neck; | 1984 |
Primary Hodgkin's disease of the lung. Case report and review of the literature.
Topics: Adult; Alcohol Drinking; Antineoplastic Combined Chemotherapy Protocols; Hodgkin Disease; Humans; Lu | 1983 |
Jaw claudication. Its value as a diagnostic clue.
Topics: Aged; Arthritis, Rheumatoid; Diagnosis, Differential; Female; Giant Cell Arteritis; Humans; Jaw Dise | 1983 |
Unusual course of painful ophthalmoplegia. Report of a case.
Topics: Abducens Nerve; Carotid Arteries; Cavernous Sinus; Cerebral Angiography; Humans; Male; Middle Aged; | 1980 |
Bites and stings of uncommon arthropods. 1. Spiders.
Topics: Adult; Antivenins; Calcium Gluconate; Child; Dexamethasone; Female; Humans; Infant; Male; Muscle Rig | 1981 |
Primary cutaneous histoplasmosis: a new presentation.
Topics: Asthma; Biopsy; Cellulitis; Histoplasmosis; Humans; Male; Middle Aged; Pain; Prednisone; Skin Ulcer | 1980 |
[Palliative treatment--prednisone for symptoms].
Topics: Brain Neoplasms; Humans; Hypercalcemia; Hypersensitivity; Nausea; Neoplasms; Pain; Palliative Care; | 1994 |
Steroid-responsive myalgia in a patient with Becker muscular dystrophy.
Topics: Adult; Antibodies, Monoclonal; Histocytochemistry; Humans; Immunohistochemistry; Male; Muscles; Musc | 1993 |
Protracted febrile myalgia in patients with familial Mediterranean fever.
Topics: Adolescent; Adult; Anti-Inflammatory Agents, Non-Steroidal; Child; Child, Preschool; Colchicine; Dru | 1994 |
Upper limb pain in chronic demyelinating polyneuropathy: electrophysiological correlates.
Topics: Arm; Demyelinating Diseases; Electric Stimulation; Female; Humans; Leg; Male; Middle Aged; Neurologi | 1994 |
Bone marrow necrosis following ALL-trans retinoic acid therapy for acute promyelocytic leukaemia.
Topics: Bone Marrow; Female; Humans; Immunologic Factors; Leukemia, Promyelocytic, Acute; Leukocyte Count; L | 1994 |
Shoulder and back pain with morning stiffness in an elderly woman.
Topics: Aged; Back Pain; Female; Humans; Pain; Polymyalgia Rheumatica; Prednisone; Shoulder | 1994 |
[Churg-Strauss syndrome].
Topics: Adult; Asthma; Back Pain; Blood Sedimentation; Bone Marrow; Churg-Strauss Syndrome; Dyspnea; Female; | 1994 |
Unstable angina in a man with joint pain.
Topics: Angina, Unstable; Arthritis, Rheumatoid; Coronary Disease; Diagnosis, Differential; Edema; Humans; M | 1993 |
Giant cell arteritis of the breast.
Topics: Aged; Anti-Inflammatory Agents; Biopsy; Breast Diseases; Diagnosis, Differential; Female; Giant Cell | 1996 |
MMC in ONS decompression.
Topics: Adolescent; Anti-Inflammatory Agents; Antibiotics, Antineoplastic; Humans; Male; Mitomycin; Myelin S | 1996 |
Pyomyositis during induction chemotherapy for acute lymphocytic leukemia.
Topics: Abscess; Antineoplastic Combined Chemotherapy Protocols; Asparaginase; Bacterial Infections; Child; | 1996 |
The sympathetic skin response in the shoulder-hand syndrome complicating tetraplegia.
Topics: Adolescent; Adult; Aged; Electrophysiology; Female; Humans; Male; Middle Aged; Pain; Prednisone; Qua | 1995 |
Acyclovir or prednisone for treating herpes zoster.
Topics: Acyclovir; Aged; Anti-Inflammatory Agents; Antiviral Agents; Drug Therapy, Combination; Evaluation S | 1996 |
Effective treatment of painful bone crises in type I gaucher's disease with high dose prednisolone.
Topics: Adolescent; Adult; Anti-Inflammatory Agents; Bone Diseases; Child; Drug Therapy, Combination; Gauche | 1996 |
Case records of the Department of Medicine University of Mississippi Medical Center. Leukocytoclastic vasculitis, probable polyarteritis nodosa, clinically indolent lymphoma, but never firmly established.
Topics: Aged; Biopsy; Connective Tissue Diseases; Cyclophosphamide; Diagnosis, Differential; Drug Therapy, C | 1997 |
Pain in Tolosa-Hunt syndrome.
Topics: Aged; Anti-Inflammatory Agents; Female; Humans; Magnetic Resonance Imaging; Orbital Pseudotumor; Pai | 1998 |
Depression and the long-term risk of pain, fatigue, and disability in patients with rheumatoid arthritis.
Topics: Arthritis, Rheumatoid; Depression; Disability Evaluation; Fatigue; Humans; Methotrexate; Pain; Predn | 1998 |
Painful Horner syndrome due to arteritis of the internal carotid artery.
Topics: Adult; Arteritis; Blepharoptosis; Carotid Arteries; Carotid Artery Diseases; Horner Syndrome; Humans | 1998 |
Use of low-dose oral prednisone to prevent paclitaxel-induced arthralgias and myalgias.
Topics: Administration, Oral; Anti-Inflammatory Agents; Antineoplastic Agents, Phytogenic; Arthralgia; Femal | 1999 |
Magnetic resonance imaging of acquired Brown syndrome in a patient with psoriasis.
Topics: Adult; Arthritis, Psoriatic; Diplopia; Eyelid Diseases; Female; Humans; Magnetic Resonance Imaging; | 1999 |
Commentary: low-dose high-frequency enzyme replacement therapy prevents fractures without complete suppression of painful bone crises in patients with severe juvenile onset type I Gaucher disease.
Topics: Adolescent; Adult; Age Factors; Animals; Anti-Inflammatory Agents; Anti-Inflammatory Agents, Non-Ste | 1998 |
From twisted ankles.
Topics: Ankle Injuries; Antineoplastic Combined Chemotherapy Protocols; Asparaginase; Burkitt Lymphoma; Cast | 1999 |
Painful tonic/dystonic spasms in Sjogren's syndrome.
Topics: Adult; Anti-Inflammatory Agents; Antibodies, Antinuclear; Arm; Dystonic Disorders; Epilepsy, General | 1999 |
Renal cholesterol microembolism: is steroid therapy effective?
Topics: Acute Kidney Injury; Anticoagulants; Coronary Thrombosis; Cortisone; Cyanosis; Embolism, Cholesterol | 2000 |
Severe and prolonged febrile myalgia in familial Mediterranean fever.
Topics: Adolescent; Adult; Chronic Disease; Familial Mediterranean Fever; Female; Fever; Glucocorticoids; Hu | 2000 |
Cyclosporin A for the treatment of patients with chronic idiopathic thrombocytopenic purpura refractory to corticosteroids or splenectomy.
Topics: Adult; Aged; Combined Modality Therapy; Cyclosporine; Drug Therapy, Combination; Female; Headache; H | 2001 |
58-year-old man with fatigue and flank pain.
Topics: Anti-Inflammatory Agents; Biopsy, Needle; Diagnosis, Differential; Fatigue; Humans; Hypercalcemia; L | 2002 |
The reflex sympathetic dystrophy syndrome. I. Clinical and histologic studies: evidence for bilaterality, response to corticosteroids and articular involvement.
Topics: Adult; Aged; Female; Humans; Joint Diseases; Middle Aged; Pain; Prednisone; Reflex Sympathetic Dystr | 1976 |
[The Tolosa-Hunt syndrome (author's transl)].
Topics: Adolescent; Humans; Male; Middle Aged; Ophthalmoplegia; Pain; Prednisone; Prognosis; Syndrome; Time | 1977 |
Tolosa-Hunt syndrome with sellar erosion.
Topics: Cavernous Sinus; Cerebral Angiography; Humans; Male; Middle Aged; Ophthalmoplegia; Pain; Prednisone; | 1979 |
[Painful ophthalmoplegia. Tolosa-Hunt syndrome].
Topics: Diagnosis, Differential; Humans; Ophthalmoplegia; Pain; Prednisone; Syndrome | 1979 |
Painful ophthalmoplegia.
Topics: Adult; Female; Humans; Male; Middle Aged; Ophthalmoplegia; Pain; Prednisone; Syndrome; Zambia | 1977 |
Painful ophthalmoplegia. The Tolusa-Hunt syndrome.
Topics: Adult; Diagnosis, Differential; Humans; Male; Ophthalmoplegia; Pain; Prednisone; Syndrome | 1978 |
[Prognosis and therapy of multiple myeloma].
Topics: Blood Transfusion; Cyclophosphamide; Drug Therapy, Combination; Humans; Melphalan; Multiple Myeloma; | 1978 |
A puzzling arthralgia.
Topics: Biopsy; Female; Hepatitis; Humans; Joint Diseases; Liver; Liver Function Tests; Middle Aged; Pain; P | 1978 |
Aseptic necrosis presenting as wrist pain in SLE.
Topics: Adolescent; Adult; Carpal Bones; Child; Diagnosis, Differential; Diagnostic Errors; Humans; Lupus Er | 1977 |
Multiple myeloma: uncommon or uncommonly diagnosed?
Topics: Adult; Anemia; Blood Sedimentation; Bone Diseases; Female; Humans; Male; Melphalan; Middle Aged; Mul | 1977 |
Hepatitis-associated lipid storage myopathy.
Topics: Adult; Biopsy; Female; Hepatitis B; Hepatitis B Surface Antigens; Humans; Lipid Metabolism, Inborn E | 1977 |
Carotid system arteritis: an overlooked and misdiagnosed syndrome.
Topics: Adult; Arteritis; Carotid Artery Diseases; Diagnosis, Differential; Face; Female; Head; Humans; Male | 1975 |
Multiple myeloma: review of 869 cases.
Topics: Adult; Aged; Bacterial Infections; Blood Cell Count; Blood Sedimentation; Bone and Bones; Calcium; C | 1975 |
Arterial stationary wave phenomenon in Tolosa-Hunt syndrome.
Topics: Adolescent; Arteritis; Carotid Artery, Internal; Cerebral Angiography; Cerebral Arteries; Female; Hu | 1975 |
Diseases of the central nervous system. Relief of pain: headache, facial neuralgia, migraine, and phantom limb.
Topics: Analgesics; Aspirin; Carbamazepine; Ergotamines; Facial Neuralgia; Giant Cell Arteritis; Headache; H | 1975 |
[Administration of Hylase in Bechterew's disease].
Topics: Adult; Carnitine; Drug Synergism; Humans; Hyaluronoglucosaminidase; Injections, Intravenous; Male; P | 1975 |
Systemic necrotizing vasculitis in nine young beagles.
Topics: Animals; Dog Diseases; Dogs; Female; Male; Pain; Polyarteritis Nodosa; Prednisone; Syndrome | 1992 |
Steroid-responsive tubular aggregate myopathy.
Topics: Biopsy; Humans; Male; Microtubules; Middle Aged; Muscle Cramp; Muscles; Pain; Prednisone; Sarcoplasm | 1991 |
L-tryptophan induced eosinophilia-myalgia syndrome.
Topics: Activities of Daily Living; Adult; Aged; Cell Count; Electrophysiology; Eosinophilia; Female; Humans | 1990 |
Eosinophilia-myalgia syndrome associated with L-tryptophan use.
Topics: Adult; Aged; Cell Count; Child; Eosinophilia; Eosinophils; Fatigue; Female; Humans; Male; Middle Age | 1990 |
Adjunctive use of hydroxychloroquine in childhood dermatomyositis.
Topics: Adolescent; Antineoplastic Agents; Child; Dermatomyositis; Drug Therapy, Combination; Female; Humans | 1989 |
Treatment of metastatic prostatic cancer with low-dose prednisone: evaluation of pain and quality of life as pragmatic indices of response.
Topics: Aged; Analgesics; Androgens; Humans; Male; Middle Aged; Neoplasm Metastasis; Pain; Prednisone; Prosp | 1989 |
Optic neuropathy associated with chronic lymphomatous meningitis.
Topics: Biopsy; Bone Marrow; Chronic Disease; Eye; Humans; Lymphoma; Male; Meningitis; Middle Aged; Nasal Mu | 1988 |
Recurrent abdominal pain and ascites in an adolescent.
Topics: Abdomen; Adolescent; Ascites; Eosinophilia; Gastroenteritis; Humans; Male; Pain; Prednisone; Recurre | 1988 |
M-2 protocol for melphalan-resistant and relapsing multiple myeloma.
Topics: Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Bone and Bones; Bone Marrow; Carmustine | 1988 |
Odynophagia from aphthous ulcers of the pharynx and esophagus in the acquired immunodeficiency syndrome (AIDS).
Topics: Acquired Immunodeficiency Syndrome; Adolescent; Adult; Deglutition Disorders; Esophageal Diseases; H | 1988 |
Severe arthralgias after wide fluctuation in corticosteroid dosage.
Topics: Adult; Female; Humans; Joint Diseases; Knee Joint; Male; Methylprednisolone; Middle Aged; Pain; Pred | 1986 |
Steroid effects on the course of abdominal pain in children with Henoch-Schonlein purpura.
Topics: Abdomen; Child; Humans; IgA Vasculitis; Pain; Prednisone; Retrospective Studies; Time Factors | 1987 |
A new etiology for visual impairment and chronic headache. The Tolosa-Hunt syndrome may be only one manifestation of venous vasculitis.
Topics: Adolescent; Adult; Aged; Chronic Disease; Female; Headache; Humans; Male; Middle Aged; Ophthalmopleg | 1986 |
Metoclopramide in vincristine-induced ileus.
Topics: Aged; Constipation; Gastrointestinal Motility; Humans; Intestinal Obstruction; Leukemia, Lymphoid; L | 1985 |
Joint and muscle pains in an aging tennis player.
Topics: Aging; Humans; Male; Middle Aged; Pain; Polymyalgia Rheumatica; Prednisone; Tennis | 1985 |
Progressive diaphyseal dysplasia: evaluation of corticosteroid therapy.
Topics: Adolescent; Adult; Camurati-Engelmann Syndrome; Child; Child, Preschool; Drug Administration Schedul | 1985 |
Idiopathic eosinophilic myositis with preexisting fibromyalgia.
Topics: Aged; Eosinophilia; Female; Humans; Joint Diseases; Muscular Diseases; Myositis; Pain; Prednisone | 1985 |
Aseptic bone/bone marrow necrosis in leukaemia.
Topics: Adolescent; Adult; Aged; Autopsy; Bone Diseases; Bone Marrow Diseases; Child; Child, Preschool; Fema | 1985 |
Letter: Acute arthralgia following high-dose intravenous methylprednisolone therapy.
Topics: Acute Disease; Administration, Oral; Adult; Female; Graft Rejection; Humans; Injections, Intravenous | 1974 |
Letter: Acute arthralgia after high-dose intravenous methylprednisolone.
Topics: Adult; Azathioprine; Drug Therapy, Combination; Female; Foreign-Body Reaction; Graft Rejection; Huma | 1974 |
The drug therapy of ulcerative colitis and of Crohn's disease.
Topics: Adrenocorticotropic Hormone; Atropine; Azathioprine; Colitis, Ulcerative; Crohn Disease; Diarrhea; D | 1974 |
Tegretol for pain in the Guillain-Barré syndrome.
Topics: Dibenzazepines; Female; Humans; Middle Aged; Pain; Polyradiculopathy; Prednisone | 1970 |
Familial brachial neuropathy. Two case reports with discussion.
Topics: Adolescent; Arm; Brachial Plexus; Follow-Up Studies; Humans; Male; Muscular Diseases; Neural Conduct | 1971 |
[Peripheral neurologic manifestations of sarcoidosis].
Topics: Adrenal Cortex Hormones; Adult; Cauda Equina; Diagnosis, Differential; Fatigue; Humans; Leg; Male; N | 1972 |
Periarteritis nodosa. A remission achieved with combined prednisone and azathioprine therapy.
Topics: Abdomen, Acute; Adolescent; Azathioprine; Eosinophilia; Humans; Male; Neuritis; Pain; Polyarteritis | 1971 |
Lymphosarcomatous arthropathy.
Topics: Arthritis; Biopsy; Cyclophosphamide; Female; Foot; Hand; Hematocrit; Humans; Lymphoma, Non-Hodgkin; | 1974 |
Alternate-day corticosteroid therapy in juvenile chronic polyarthritis.
Topics: Adolescent; Anemia; Arthritis, Juvenile; Body Height; Child; Child, Preschool; Chronic Disease; Drug | 1974 |
[Experiences and results in the treatment of acute pancreatitis].
Topics: Acute Disease; Aged; Analgesics; Anti-Bacterial Agents; Aprotinin; Blood Transfusion; Female; Humans | 1974 |
Tolosa-Hunt syndrome and antinuclear factor.
Topics: Antibodies, Antinuclear; Blood Sedimentation; Female; Fluorescent Antibody Technique; Humans; Middle | 1974 |
The Tolosa-Hunt syndrome (painful ophthalmoplegia) in children.
Topics: Blepharoptosis; Child; Child, Preschool; Female; Headache; Humans; Male; Ophthalmoplegia; Pain; Pred | 1973 |
[Painful ophthalmoplegia. Report of 3 cases].
Topics: Adolescent; Adult; Carotid Arteries; Cerebral Angiography; Dexamethasone; Diagnosis, Differential; F | 1974 |
Temporal arteritis.
Topics: Age Factors; Aged; Angiography; Biopsy; Blindness; Blood Proteins; Blood Sedimentation; Carotid Arte | 1974 |
[On the treatment of inflammatory and degenerative diseases of the musculosketetal system with Vertebran].
Topics: Atropine; Bone Diseases; Caffeine; Ergoloid Mesylates; Humans; Joint Diseases; Muscular Diseases; Pa | 1968 |
Polyarthritis associated with Yersinia enterocolitica infection. Clinical features and laboratory findings in nine cases with severe joint symptoms.
Topics: Adult; Agglutination Tests; Anti-Bacterial Agents; Arthritis, Infectious; Complement Fixation Tests; | 1972 |
[Painful ophthalmoplegia].
Topics: Adult; Aged; Cerebral Angiography; Cerebrovascular Disorders; Humans; Male; Migraine Disorders; Opht | 1972 |
[Severe anguilluliatis revealed by corticosteroid therapy. Case].
Topics: Adult; Anorexia Nervosa; Biopsy; Blood Proteins; Diarrhea; Eosinophils; Female; Humans; Jejunum; Pai | 1972 |
Recurrent right middle lobe syndrome in an asthmatic child. Case report and serial vectorcardiographic study.
Topics: Asthma; Child; Cough; Ephedrine; Female; Humans; Middle Lobe Syndrome; Pain; Phenobarbital; Predniso | 1970 |
Corticosteroids in the treatment of Engelmann's disease: progressive diaphyseal dysplasia.
Topics: Bone Resorption; Child, Preschool; Cortisone; Exostoses; Female; Femur; Fibula; Gait; Growth; Havers | 1970 |
[Löfgren's syndrome (acute sarcoidosis)].
Topics: Acute Disease; Adult; Biopsy; Cardiomyopathies; Erythema Nodosum; Female; Humans; Hypersensitivity; | 1970 |
Pericarditis in chronic uremia and its sequels.
Topics: Adolescent; Adult; Age Factors; Arrhythmias, Cardiac; Autopsy; Blood Urea Nitrogen; Body Weight; Chr | 1971 |
Report of a case of sphenoid fissure syndrome studied by orbital venography.
Topics: Adolescent; Blepharoptosis; Cavernous Sinus; Centrifugation, Density Gradient; Constriction; Female; | 1971 |
Myopathy of hypothyroidism.
Topics: Adult; Aged; Antibodies; Female; Humans; Hypothyroidism; Male; Middle Aged; Muscular Atrophy; Muscul | 1968 |
[On the phlogogenic properties of lactic acid in animal experiments].
Topics: Animals; Capillary Permeability; Conjunctivitis; Edema; Exudates and Transudates; Guinea Pigs; Infla | 1968 |
Giant cell arteritis with polymyalgia rheumatica, loss of vision, and abdominal symptoms occurring during a four year course.
Topics: Aged; Blindness; Blood Sedimentation; Diarrhea; Gastrointestinal Diseases; Giant Cell Arteritis; Hum | 1969 |
Painful ophthalmoplegia. The Tolosa-Hunt syndrome.
Topics: Cranial Nerves; Diagnosis, Differential; Diplopia; Eye Diseases; Female; Humans; Male; Middle Aged; | 1966 |