- Trials with a EudraCT protocol (374)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (10)
374 result(s) found for: Osteoarthritis.
Displaying page 15 of 19.
| EudraCT Number: 2010-023888-17 | Sponsor Protocol Number: OMS103-MEN-003 | Start Date*: 2011-05-11 | |||||||||||
| Sponsor Name:Omeros Corporation | |||||||||||||
| Full Title: A Randomized, Double-Blind, Parallel Group, Vehicle-Controlled Study to Evaluate the Safety and Efficacy of OMS103HP-S Administered in Joint Irrigation Solution to Subjects Undergoing Arthroscopic ... | |||||||||||||
| Medical condition: Arthroscopic surgery | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-024010-61 | Sponsor Protocol Number: DRO/IV-ART-01 | Start Date*: 2011-11-09 | |||||||||||
| Sponsor Name:BIOIBERICA, S.A. | |||||||||||||
| Full Title: NON-INFERIORITY CLINICAL TRIAL ON THE EFFICACY AND SAFETY OF CHONDROITIN SULFATE AND GLUCOSAMINE HYDROCHLORIDE IN COMBINATION VERSUS CELECOXIB IN PATIENTS WITH KNEE OSTEOARTHRITIS | |||||||||||||
| Medical condition: KNEE OSTEOARTHRITIS | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Completed) ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-000893-27 | Sponsor Protocol Number: 230205 | Start Date*: 2005-09-02 |
| Sponsor Name:Prof. Gustav Dobos, Kliniken Essen Mitte | ||
| Full Title: Effectiveness of leech therapy in epicondylitis humeroradialis - a randomized controlled trial | ||
| Medical condition: In the planned study patients with painful epicondylitis humeroradialis of the ellbow are treated with leeches or a standard treatment. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-003669-18 | Sponsor Protocol Number: SVS/K/00604 | Start Date*: 2006-11-15 |
| Sponsor Name:Seven Seas Limited | ||
| Full Title: Efficacy an tolerability of a combinatzion of glucosamine sulphate and the tw omega-3 unsaturated fatty acids EPA and DHA in comparison to glucosamine sulphate in patients with ostearthritis | ||
| Medical condition: Osteoarthritis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-003009-10 | Sponsor Protocol Number: PRG-BUP-03/02 | Start Date*: 2005-08-05 |
| Sponsor Name:Barts and The London NHS Trust | ||
| Full Title: A randomized, open label pilot study to investigate the effect of chronic administration of buprenorphine prior to arthroplasty on the opioid requirements of patients intraoperatively and postopera... | ||
| Medical condition: Patients with severe chronic pain due to osteoarthritis of the knee or hip, awaiting surgical joint replacement surgery. ICD10: M16.50 & M17.30 | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-001580-30 | Sponsor Protocol Number: 2006.SUR.ORT.01 | Start Date*: 2006-10-13 |
| Sponsor Name:Royal Cornwall Hospitals NHS Trust | ||
| Full Title: Investigation into the effects of steroid and local anaesthetic infiltration into soft tissues in total hip replacement wounds on post-operative pain relief. | ||
| Medical condition: patients undergoing total hip replacement surgery for osteoarthritis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-004301-28 | Sponsor Protocol Number: HUM 04-040 | Start Date*: 2006-08-24 |
| Sponsor Name:KAS Glostrup | ||
| Full Title: Treatment of painful knee osteoarthrosis with adalimumab (Humira (R)): Open-label study to evaluate safety and efficacy | ||
| Medical condition: Osteoarthrosis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-005082-31 | Sponsor Protocol Number: MP-TAP-2016-01 | Start Date*: 2017-11-20 |
| Sponsor Name:MRI Research Unit, Radiology Department. Hospital del Mar. | ||
| Full Title: Assessment of Tapentadol effects on patients with pain central sensitization using functional MRI | ||
| Medical condition: Patients suffering from pain due to knee osteoarthritis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-017470-20 | Sponsor Protocol Number: GRT-CG5503-2009-02-FR | Start Date*: 2010-05-07 | |||||||||||
| Sponsor Name:Laboratoires Grünenthal | |||||||||||||
| Full Title: An open-label extension study for patients with severe chronic low back pain or severe chronic pain due to knee osteoarthritis who have completed any of the previous phase IIIb trials with tapentad... | |||||||||||||
| Medical condition: Severe chronic pain | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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 | |||||||||||||
| EudraCT Number: 2019-000757-31 | Sponsor Protocol Number: 2018/728 | Start Date*: 2019-08-30 |
| Sponsor Name:Martina Hansens Hospital | ||
| Full Title: A RANDOMIZED PLACEBO CONTROLLED TRIAL TESTING THE EFFECTS OF ZOLEDRONIC ACID ON HIP OSTEOARTHRITIS | ||
| Medical condition: Investigated disease is osteoarthritis of the hip with concurrent Bone marrow lesions | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NO (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-002645-37 | Sponsor Protocol Number: KC706-C05 | Start Date*: 2006-08-25 | |||||||||||
| Sponsor Name:Kémia, Inc. | |||||||||||||
| Full Title: A Phase II randomized double-blind placebo-controlled Study of KC706 in patients with rheumatoid arthritis inadequately controlled with a stable dose of methotrexate | |||||||||||||
| Medical condition: Active rheumatoid arthritis (RA), patients taking stable doses of methotrexate | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-000624-20 | Sponsor Protocol Number: ILONA | Start Date*: 2021-06-17 | |||||||||||
| Sponsor Name:Leipzig University | |||||||||||||
| Full Title: Core decompression versus core decompression followed by infusion of Iloprost in the treatment of non-traumatic avascular necrosis of the femoral head | |||||||||||||
| Medical condition: non-traumatic avascular necrosis of the femoral head (N-ANFH) | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-005889-17 | Sponsor Protocol Number: WATOS-PE | Start Date*: 2023-05-22 |
| Sponsor Name:Fundació Institut d'Investigació i Innovació Parc Taulí (I3PT) | ||
| Full Title: PAIN CONTROL WITH THE USE OF WALANT IN TOTAL TRAPEZECTOMY. RANDOMIZED CLINICAL TRIAL | ||
| Medical condition: Thumb trapeziometacarpal joint osteoarthritis treated by total trapeziectomy | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-001234-17 | Sponsor Protocol Number: A3191084 | Start Date*: 2006-06-15 | |||||||||||
| Sponsor Name:Pfizer Limited | |||||||||||||
| Full Title: Double-blind, triple dummy, parallel-group, randomized, six-month study to compare celecoxib (200 mg BID) with diclofenac SR (75 mg BID) plus omeprazole (20 mg QD) for gastrointestinal events in su... | |||||||||||||
| Medical condition: Treatment of osteoarthritis (OA) and/or rheumatoid arthritis (RA) in high GI risk patients | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) ES (Completed) BE (Completed) SE (Completed) CZ (Completed) LT (Completed) DE (Suspended by CA) EE (Completed) PT (Completed) GR (Completed) IE (Completed) LV (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-004514-40 | Sponsor Protocol Number: KF5503/33-R331333-PAI-3002 | Start Date*: 2007-02-14 | |||||||||||
| Sponsor Name:Johnson & Johnson Pharamceutical Research & Development, L.L.C. | |||||||||||||
| Full Title: A Randomized, Double-Blind, Active- And Placebo-Controlled, Parallel Group, Multicenter Study To Evaluate The Efficacy And Safety of Multiple Doses of CG5503 Immediate Release Formulation In Subjec... | |||||||||||||
| Medical condition: Pain | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-006911-60 | Sponsor Protocol Number: 42801PAI3001 | Start Date*: 2007-06-15 | |||||||||||
| Sponsor Name:Janssen-Cilag International N.V. | |||||||||||||
| Full Title: Randomised, double-blind, placebo-controlled, parallel-group trial to investigate the analgesic effect of OROS hydromorphone hydrochloride in comparison with placebo in subjects with moderate to se... | |||||||||||||
| Medical condition: moderate to severe pain induced by osteoarthritis of the hip or the knee | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) GB (Completed) SK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-005082-34 | Sponsor Protocol Number: A2620383 | Start Date*: 2007-12-14 |
| Sponsor Name:GlaxoSmithKline Consumer Healthcare | ||
| Full Title: A Proof of Principle Study to Investigate the Efficacy of a Medical Device and Topical Analgesic Combination for the Treatment of Pain and Performance Related Function in Osteoarthritis | ||
| Medical condition: To compare the efficacy of 72 hours (hrs) treatment of topical diclofenac plus a heat patch with 72 hrs treatment of topical diclofenac plus a placebo patch on the primary endpoint of mobility in p... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-000503-33 | Sponsor Protocol Number: 01-05 | Start Date*: 2005-09-02 |
| Sponsor Name:Department Integrative Medicine, Kliniken Essen Mitte | ||
| Full Title: Effectiveness of leech therapy in osteoarthritis of the thumb joint (rhizarthrosis) - a randomized controlled trial | ||
| Medical condition: Leeches therapy has been successully evaluated in symptomatic knee osteoarthrits for pain relief. In the planned study patients with painful rhizarthrosis (arthrosis of the thumb joint) will be rec... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-011492-73 | Sponsor Protocol Number: 13.09 | Start Date*: 2009-09-28 |
| Sponsor Name:Swindon and Marlborough NHS Foundation Trust | ||
| Full Title: Analysis of Blood Loss With the Use of Fibrin Sealant in Total Knee Replacement Surgery – A Randomised Controlled Study | ||
| Medical condition: Blood loss in total knee arthroplasty | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
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