- Trials with a EudraCT protocol (228)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
228 result(s) found for: Osteoarthritis, Knee AND Pain.
Displaying page 3 of 12.
EudraCT Number: 2015-003230-26 | Sponsor Protocol Number: MIV-711-201 | Start Date*: 2016-03-23 | |||||||||||
Sponsor Name:Medivir AB | |||||||||||||
Full Title: A Randomised, Double-blind Placebo-controlled Phase IIa Study to Evaluate Efficacy, Safety and Tolerability of MIV-711 in Knee Joint Osteoarthritis | |||||||||||||
Medical condition: Knee Joint Osteoarthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-005254-53 | Sponsor Protocol Number: BKOS-03 | Start Date*: 2012-05-14 | |||||||||||
Sponsor Name:Menarini Ricerche S.p.A | |||||||||||||
Full Title: A double-blind, randomised, placebo controlled, sequential ascending dose study, to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of single intra-articular doses of fasi... | |||||||||||||
Medical condition: Ostoarthritis of the knee | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002607-18 | Sponsor Protocol Number: 101.04 | Start Date*: 2012-08-30 | |||||||||||
Sponsor Name:Marius Henriksen | |||||||||||||
Full Title: COMBINED INTRA ARTICULAR CORTICOSTEROID AND EXERCISE IN PATIENTS WITH OSTEOARTHRITIS OF THE KNEE: A RANDOMISED TRIAL | |||||||||||||
Medical condition: Knee Osteoarthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004718-27 | Sponsor Protocol Number: INRETRAM3/2014 | Start Date*: 2017-01-11 | ||||||||||||||||
Sponsor Name:Medical Unviersity of Warsaw | ||||||||||||||||||
Full Title: A randomised, multicenter, single-blinded, parallel-group study to assess efficacy, safety and tolerability of the combination of Immediate Release (IR) tramadol with micronized magnesium lactate a... | ||||||||||||||||||
Medical condition: Chronic knee and/or hip pain due to Osteoarthritis. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: PL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000818-37 | Sponsor Protocol Number: MTX-071-P03 | Start Date*: 2018-06-28 | |||||||||||||||||||||
Sponsor Name:Grünenthal GmbH | |||||||||||||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, single dose phase IIb exploratory study to document the clinical effects and safety of intra-articular injections of Lopain (MTX-071) in patients wit... | |||||||||||||||||||||||
Medical condition: chronic osteoarthritic knee joint pain | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: AT (Completed) SK (Completed) HR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-000859-39 | Sponsor Protocol Number: EP-104IAR-201 | Start Date*: 2021-09-01 | |||||||||||
Sponsor Name:Eupraxia Pharmaceuticals Inc. | |||||||||||||
Full Title: A Phase 2, Randomized, Double-Blind, Vehicle-Controlled Study Evaluating the Safety, Efficacy and Pharmacokinetics of Single Dose EP-104IAR for 24 Weeks in Patients with Osteoarthritis of the Knee | |||||||||||||
Medical condition: Osteoarthritis of the knee | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-014516-35 | Sponsor Protocol Number: L00023 GE 303 | Start Date*: 2009-12-01 | |||||||||||
Sponsor Name:PIERRE FABRE MEDICAMENT | |||||||||||||
Full Title: EFFICACY AND TOLERABILITY OF CHONDROITIN SULPHATE 1000MG, TWICE DAILY IN PATIENTS WITH SYMPTOMATIC KNEE OSTEOARTHRITIS | |||||||||||||
Medical condition: Symptomatic knee osteoarthtitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) LT (Completed) BE (Completed) EE (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003485-33 | Sponsor Protocol Number: F1J-MC-HMFG | Start Date*: 2007-03-21 | |||||||||||
Sponsor Name:Eli Lilly and Company Limited | |||||||||||||
Full Title: Duloxetine 60 to 120 mg versus Placebo in the Treatment of Patients with Osteoarthritis Knee Pain | |||||||||||||
Medical condition: Osteoarthritis Knee Pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001981-24 | Sponsor Protocol Number: MTX-071-P01 | Start Date*: 2016-02-04 | |||||||||||||||||||||
Sponsor Name:Mestex | |||||||||||||||||||||||
Full Title: Lopain (MTX-071 / resiniferatoxin) An open label, dose-escalating phase I/IIa study to determine the safety and clinical effects of intra-articular injections of Lopain (MTX-071) in patients wi... | |||||||||||||||||||||||
Medical condition: Chronic osteoarthritic knee-joint pain | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-001411-71 | Sponsor Protocol Number: R475-OA-1815 | Start Date*: 2018-12-03 | |||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | |||||||||||||
Full Title: Study to Evaluate Synovial Fluid in the Phase 3 Fasinumab Program for Osteoarthritis of the Knee and Hip | |||||||||||||
Medical condition: Pain due to osteoarthritis of the knee | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002144-27 | Sponsor Protocol Number: M12-146 | Start Date*: 2012-07-02 | |||||||||||
Sponsor Name:Abbott GmbH & Co. KG | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo and Active-Controlled Study Comparing the Safety and Analgesic Efficacy of ABT-110 to Placebo in Subjects with Pain from Osteoarthritis of the Knee | |||||||||||||
Medical condition: Pain from Osteoarthritis of the Knee | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) PL (Prematurely Ended) IT (Prematurely Ended) FI (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003875-35 | Sponsor Protocol Number: GO-ON-01 | Start Date*: 2009-03-24 | |||||||||||
Sponsor Name:Rottapharm SpA | |||||||||||||
Full Title: Comparative study of efficacy and safety of GO-ON and Hyalgan in patients with symptomatic osteoarthritis of the knee. | |||||||||||||
Medical condition: Patients with symptomatic osteoarthritis of the knee. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005398-22 | Sponsor Protocol Number: ARACONDRO-001 | Start Date*: 2012-10-11 | |||||||||||
Sponsor Name:ARAFARMA GROUP, S.A. | |||||||||||||
Full Title: A randomized, multicenter, double-blind, double dummy and parallel study to evaluate the efficacy of the combination of Chondroitin sulfate and Glucosamine hydrochloride in a single dose chewable t... | |||||||||||||
Medical condition: Knee osteoarthritis with moderate to severe pain. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000149-12 | Sponsor Protocol Number: CXA30007 | Start Date*: 2005-04-24 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: A Phase III, 12-week, Multicentre, Double-blind, Double-dummy, Randomised, Placebo- and Active Comparator-Controlled, Parallel Group study to investigate the Efficacy and Safety of GW406381 1mg, 5m... | |||||||||||||
Medical condition: Osteoarthritis of the Knee | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) HU (Completed) DK (Completed) DE (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005914-10 | Sponsor Protocol Number: CBA109389 | Start Date*: 2007-03-22 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: A Multicentre, Randomised, Double-blind, Placebo and Naproxen (500mg) BID controlled, Phase II Proof of Concept, Parallel Group Study to Assess the Efficacy and Safety of Oral GW842166 at Two Dose ... | |||||||||||||
Medical condition: Osteoarthritis of the knee | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) ES (Completed) DK (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003059-20 | Sponsor Protocol Number: EMR700692_006 | Start Date*: 2013-07-31 | |||||||||||
Sponsor Name:Merck KGaA | |||||||||||||
Full Title: A multicenter, randomized, double-blind, placebo-controlled, parallel-group trial to investigate the efficacy and safety of different intra-articular (i.a.) dosages of sprifermin in subjects with p... | |||||||||||||
Medical condition: Primary osteoarthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) EE (Completed) DK (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022625-15 | Sponsor Protocol Number: 2010-01 | Start Date*: 2010-11-22 | |||||||||||
Sponsor Name:Laboratoires ELERTE | |||||||||||||
Full Title: Evaluation de l’efficacité de l’association ibuprofène et codéine versus l’ibuprofène seul dans le traitement de la poussée douloureuse de la gonarthrose. Etude en double aveugle, randomisée contrô... | |||||||||||||
Medical condition: Gonarthrose fémoro-tibiale uni ou bilatérale en poussée douloureuse | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002933-23 | Sponsor Protocol Number: DAR-INT-14-01 | Start Date*: 2016-05-24 | |||||||||||
Sponsor Name:TRB CHEMEDICA INTERNATIONAL SA | |||||||||||||
Full Title: AN INTERNATIONAL, MULTICENTRE, DOUBLE-BLIND, RANDOMISED STUDY OF THE EFFECT OF DIACEREIN VS CELECOXIB ON SYMPTOMS AND STRUCTURAL CHANGES IN SYMPTOMATIC KNEE OSTEOARTHRITIS PATIENTS AS ASSESSED BY M... | |||||||||||||
Medical condition: Pain reduction in symptomatic knee osteoarthritis (OA) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) ES (Completed) AT (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020475-23 | Sponsor Protocol Number: B0041007 | Start Date*: 2010-10-05 | |||||||||||
Sponsor Name:Pfizer Inc.235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A PHASE 2 RANDOMIZED, DOUBLE-BLINDED, DOUBLE-DUMMY, PLACEBO AND ACTIVE CONTROLLED TWO COHORT TWO-WAY CROSS-OVER, MULTI-CENTRE CLINICAL TRIAL TO EXAMINE THE PAIN RELIEF PRODUCED BY 2 WEEKS OF DAILY... | |||||||||||||
Medical condition: Chronic pain in patients with Osteo-arthritis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002117-30 | Sponsor Protocol Number: 000010/BT | Start Date*: 2016-02-16 | |||||||||||
Sponsor Name:Bone Therapeutics S.A. | |||||||||||||
Full Title: A Two-stage 6-month, Multicentre, Randomised, Double-blind, Controlled Study on the Safety and Efficacy of a Single Intra-articular Administration of JTA-004 in Patients with Symptomatic Knee Osteo... | |||||||||||||
Medical condition: Symptomatic osteoarthritis of the knee with Kellgren-Lawrence grade II and III | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
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