- 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 9 of 12.
EudraCT Number: 2011-002768-25 | Sponsor Protocol Number: 191622-102 | Start Date*: 2011-11-10 | |||||||||||
Sponsor Name:Allergan Limited | |||||||||||||
Full Title: A Single Center, Double-blind, Randomized, Placebo-controlled, Parallel-group Study of the Efficacy and Safety of BOTOX® (Botulinum Toxin Type A) Purified Neurotoxin Complex as Treatment for Osteoa... | |||||||||||||
Medical condition: Treatment of Osteoarthritis Knee Pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001669-16 | Sponsor Protocol Number: 80-83600-98-3143 | Start Date*: 2015-12-21 |
Sponsor Name:Erasmus MC | ||
Full Title: Duloxetine for chronic osteoarthritis pain; an important alternative? | ||
Medical condition: osteoarthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2020-000204-11 | Sponsor Protocol Number: NN9536-4578 | Start Date*: 2021-01-11 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: Effect of subcutaneous semaglutide 2.4 mg once-weekly compared to placebo in subjects with obesity and knee osteoarthritis | |||||||||||||
Medical condition: Obesity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DK (Completed) SE (Completed) NO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001713-34 | Sponsor Protocol Number: A3471119 | Start Date*: 2005-01-11 | |||||||||||
Sponsor Name:Pfizer Limited | |||||||||||||
Full Title: RANDOMIZED, DOUBLE-BLIND, MULTICENTER STUDY OF THE EFFICACY, TOLERABILITY AND SAFETY OF VALDECOXIB (BEXTRA®)10 MG OD VS. DICLOFENAC SODIUM 50 MG TDS FOR 6 WEEKS IN SUBJECTS WITH OSTEOARTHRITIS OF T... | |||||||||||||
Medical condition: Osteoarthritis of the knee | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006298-26 | Sponsor Protocol Number: CL-033-III-03 | Start Date*: 2008-04-22 | |||||||||||
Sponsor Name:IDEA AG | |||||||||||||
Full Title: Multicenter, randomized, double-blind, placebo- and active-controlled study of safety and efficacy of two dosages of epicutaneously applied Diractin® (ketoprofen in Transfersome® gel) for the treat... | |||||||||||||
Medical condition: Treatment of osteoarthritis of the knee | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001754-92 | Sponsor Protocol Number: AAE581C2201 | Start Date*: 2005-02-14 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A phase II, 12-month, double-blind, placebo-controlled, dose-finding, multicenter study to evaluate the safety, tolerability, and disease modifying efficacy of daily oral AAE581 (10, 25 and 50 mg t... | ||
Medical condition: Osteoarthritis (OA) is a disease with a complex pathophysiology leading to the degeneration of articular cartilage and bone. It is characterized by pain, biochemical and enzymatic changes, cartilag... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-002634-20 | Sponsor Protocol Number: NBF_HK_01_2018 | Start Date*: 2018-10-23 | ||||||||||||||||
Sponsor Name:Anaesthesia Department, Hvidovre Hospital, Capital Region of Denmark | ||||||||||||||||||
Full Title: Highdose steroid for total knee arthroplasty - A randomized doubleblindet controlled trial. | ||||||||||||||||||
Medical condition: Perioperative management of total knee-arthroplasty because of knee-osteoarthritis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-010425-39 | Sponsor Protocol Number: KF5503/43 | Start Date*: 2009-09-23 | |||||||||||
Sponsor Name:Grünenthal GmbH | |||||||||||||
Full Title: An evaluation of the effectiveness and tolerability of tapentadol hydrochloride prolonged release, and tapentadol hydrochloride immediate release on demand, in subjects with severe chronic pain due... | |||||||||||||
Medical condition: Pain due to Osteoarthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) DE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004999-35 | Sponsor Protocol Number: BKOS-04 | Start Date*: 2014-04-08 | |||||||||||
Sponsor Name:Menarini Ricerche S.p.A. | |||||||||||||
Full Title: A DOUBLE-BLIND, RANDOMISED, PLACEBO-CONTROLLED, FOUR PARALLEL ARM, DOSE-FINDING STUDY TO EVALUATE THE EFFICACY, SAFETY, TOLERABILITY, AND PHARMACOKINETICS OF SINGLE INTRA-ARTICULAR INJECTIONS OF FA... | |||||||||||||
Medical condition: Symptomatic osteoarthritis (OA) of the knee. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-002206-10 | Sponsor Protocol Number: APHP190891 | Start Date*: 2020-07-07 |
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | ||
Full Title: A prospective study of the safety and efficacy of the use of a Lipiodol Emulsion for the embolization of inflammatory hypervascularizations observed in patients with articular or abarticular pain i... | ||
Medical condition: Adult patients with articular or abarticular intractable pain in the knee | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-020748-37 | Sponsor Protocol Number: BUP4504 | Start Date*: 2010-12-01 | |||||||||||
Sponsor Name:Mundipharma AB | |||||||||||||
Full Title: An open label, multi-centre, prospective age-group-controlled study to evaluate efficacy and safety of buprenorphine transdermal patches in subjects with chronic, moderate to severe osteoarthritis ... | |||||||||||||
Medical condition: Osteoarthritis pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005946-35 | Sponsor Protocol Number: EFC10096 | Start Date*: 2007-05-17 |
Sponsor Name:sanofi-aventis recherche & développement | ||
Full Title: Efficacy and safety of 3 intra-articular injections of 500 µg icatibant in a randomized, double-blind, parallel-group, placebo-controlled 13-week multi-centre study in patients with symptomatic kne... | ||
Medical condition: patients with painful OA in the knee | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-004973-25 | Sponsor Protocol Number: PIAS005/06 | Start Date*: 2008-05-28 |
Sponsor Name:Laboratoire Expanscience | ||
Full Title: Prospective multicentric open clinical study comparing the efficacy and safety of piascledine 300 plus standard treatment versus standard treatment only in patients with osteoarthritis of the knee | ||
Medical condition: Osteoarthritis of the knee | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: PL (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-001008-13 | Sponsor Protocol Number: 497 | Start Date*: 2013-09-18 |
Sponsor Name:Sint Maartenskliniek | ||
Full Title: Fast-track rehabilitation protocol for Total Knee Arthroplasty: A Randomized Controlled Trial comparing Local Infiltration Analgesia with Femoral Nerve Block | ||
Medical condition: patients requiring total knee arthroplasty for non-inflammatory osteoarthritis of the knee | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-004052-30 | Sponsor Protocol Number: CLNA043X2202 | Start Date*: 2017-04-28 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A randomized, placebo-controlled, patient and investigator blinded, Proof of Concept study investigating the safety, tolerability and preliminary efficacy of multiple intra-articular LNA043 injecti... | |||||||||||||
Medical condition: Acute cartilage injuries | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) CZ (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004730-15 | Sponsor Protocol Number: R5069-OA-1849 | Start Date*: 2019-08-08 |
Sponsor Name:Regeneron Pharmaceuticals, Inc. | ||
Full Title: A Randomized, Double-Blind, Multi-Dose, Placebo-Controlled Study to Evaluate the Efficacy and Safety of REGN5069 in Patients with Pain due to Osteoarthritis of the Knee | ||
Medical condition: Pain due to osteoarthritis of the knee | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) PL (Prematurely Ended) BG (Prematurely Ended) ES (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2005-004270-25 | Sponsor Protocol Number: A3191173 | Start Date*: 2005-12-09 | |||||||||||
Sponsor Name:Pfizer Ltd | |||||||||||||
Full Title: Double-blind, parallel-group, randomized, study of the efficacy and safety of continuous use of celecoxib vs the “usual use” of celecoxib in the treatment of subjects with chronicosteoarthritis of ... | |||||||||||||
Medical condition: Osteoarthritis of knee or hip joint | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000414-39 | Sponsor Protocol Number: BUP4203 | Start Date*: 2004-08-10 | |||||||||||
Sponsor Name:Mundipharma OY | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, parallel group, multicenter study to evaluate the long-term efficacy and safety of Norspan® versus placebo Norspan in subjects with chronic, moderate... | |||||||||||||
Medical condition: Chronic, moderate to severe osteoarthritis pain of the hip and/or knee. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005596-90 | Sponsor Protocol Number: NL51548.100.14 | Start Date*: 2015-04-22 |
Sponsor Name:St. Lucas Andreas Hospital | ||
Full Title: Comparison of femoral nerve block with posterior capsule infiltration versus anterior and posterior capsule infiltration after total knee replacement. | ||
Medical condition: patienst requiring total knee replacement for non-inflammatory osteoarthritis of the knee | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000538-31 | Sponsor Protocol Number: Neuroimpa2015 | Start Date*: 2015-06-01 | |||||||||||
Sponsor Name:Charité University medicine Berlin | |||||||||||||
Full Title: NEUORIMPA - Intraarticular Application of Opioids in Chronic Arthritis of the knee joint | |||||||||||||
Medical condition: chronic arthritis of the knee joint effusion as part of spondyloarthritis (Assessments in SpondyloArthritis international Society, ASAS criteria), Rheumatoid Arthritis, RA (according to American Co... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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