- Trials with a EudraCT protocol (133)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
133 result(s) found for: Osteoarthritis, Hip.
Displaying page 1 of 7.
EudraCT Number: 2013-001830-16 | Sponsor Protocol Number: 42160443PAI3001 | Start Date*: 2015-11-11 | ||||||||||||||||
Sponsor Name:Janssen-Cilag International NV | ||||||||||||||||||
Full Title: Randomized, 16-Week, Multi-Phase, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety, and Tolerability of Fulranumab as Adjunctive Therapy in Subjects with Signs and Symptoms o... | ||||||||||||||||||
Medical condition: Osteoarthritis of the Hip or Knee | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) GB (Completed) HU (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-004796-39 | Sponsor Protocol Number: PT-SM-14-OA | Start Date*: 2013-04-30 | ||||||||||||||||
Sponsor Name:Fondazione IRCCS Policlinico San Matteo | ||||||||||||||||||
Full Title: A Comparative Study of Oxycodone/Naloxone versus Codeine/Paracetamol in the Treatment of Moderate to Severe Chronic Knee and/or hip Pain Due to Osteoarthritis | ||||||||||||||||||
Medical condition: Moderate to Severe Chronic Knee and/or hip Pain Due to Osteoarthritis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000508-15 | Sponsor Protocol Number: L00023 GE 404 | Start Date*: 2005-10-06 | |||||||||||
Sponsor Name:PIERRE FABRE MEDICAMENT | |||||||||||||
Full Title: Efficacy and safety assessment of 6 months (24 weeks) treatment with Structum® 500 mg capsule bid in hip osteoarthritis: multicenter randomised double blind parallel group and placebo controlled st... | |||||||||||||
Medical condition: Patients with osteoarthritis of the hip | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004931-25 | Sponsor Protocol Number: INDEX | Start Date*: 2021-09-10 | ||||||||||||||||
Sponsor Name:Turku University Hospital | ||||||||||||||||||
Full Title: Intranasal dexmedetomidine pharmacokinetics on patients under general anesthesia | ||||||||||||||||||
Medical condition: Knee osteoarthritis Hip osteoarthritis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022106-40 | Sponsor Protocol Number: NL29912.099.09 | Start Date*: 2014-06-10 | |||||||||||
Sponsor Name: | |||||||||||||
Full Title: Longterm Effects of Intraarticular Hyaluronan vs Corticosteroid in Osteoarthritis of the Hip: A Randomized Controlled Trial | |||||||||||||
Medical condition: coxarthrosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004484-18 | Sponsor Protocol Number: 30062008 | Start Date*: 2008-09-16 | |||||||||||
Sponsor Name:Hannu Kokki | |||||||||||||
Full Title: Suun kautta annosteltavan etorikoksibin ja laskimoon annosteltavan ketoprofeenin aivoselkäydinnestepitoisuudet ja niiden vaikutus prostaglandiini-E2-pitoisuuksiin aikuisten lonkan tekonivelleikkauk... | |||||||||||||
Medical condition: Tutkimukseen otettavat potilaat ovat perusterveitä, primääriin lonkan tekonivelleikkaukseen tulevia henkilöitä | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2017-001028-23 | Sponsor Protocol Number: T1010-01 | Start Date*: 2017-08-02 | ||||||||||||||||
Sponsor Name:Tools4Patient | ||||||||||||||||||
Full Title: Validation Study to Investigate the Effect of T4P1010 treatment in Patients with Osteoarthritic Pain of Knee or Hip. | ||||||||||||||||||
Medical condition: Osteoarthritic pain of knee or hip. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-002598-13 | Sponsor Protocol Number: 42160443PAI3003 | Start Date*: 2015-06-24 | ||||||||||||||||
Sponsor Name:Janssen-Cilag International N.V. | ||||||||||||||||||
Full Title: Randomized, 16-Week, Multi-Phase, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety, and Tolerability of Fulranumab as Monotherapy in Subjects with Signs and Symptoms of Osteo... | ||||||||||||||||||
Medical condition: Osteoarthritis of the Hip or Knee | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) BE (Completed) CZ (Prematurely Ended) GB (Completed) NL (Completed) PL (Completed) FR (Completed) SK (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-003879-37 | Sponsor Protocol Number: 42160443PAI3002 | Start Date*: 2015-07-17 | ||||||||||||||||
Sponsor Name:Janssen-Cilag International NV | ||||||||||||||||||
Full Title: Randomized, 16-Week, Multi-Phase, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety, and Tolerability of Fulranumab as Monotherapy in Subjects with Signs and Symptoms of Osteo... | ||||||||||||||||||
Medical condition: Osteoarthritis of the Hip or Knee | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-003224-40 | Sponsor Protocol Number: 42160443PAI3007 | Start Date*: 2015-11-11 | ||||||||||||||||
Sponsor Name:Janssen-Cilag International N.V. | ||||||||||||||||||
Full Title: Randomized, 16-Week, Multi-Phase, Double-Blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability, and Efficacy of Fulranumab as Adjunctive Therapy in Subjects with Signs and Symptoms o... | ||||||||||||||||||
Medical condition: Osteoarthritis of the Hip or Knee | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) ES (Prematurely Ended) CZ (Prematurely Ended) HU (Completed) SE (Completed) PL (Completed) GB (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-004313-41 | Sponsor Protocol Number: 47659 | Start Date*: 2014-05-19 | |||||||||||||||||||||
Sponsor Name:UMCG | |||||||||||||||||||||||
Full Title: Effect of pre-operative pain treatment by means of duloxetine on postoperative outcome after total hip or knee arthroplasty | |||||||||||||||||||||||
Medical condition: Osteoarthritis (knee or hip) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003826-28 | Sponsor Protocol Number: Z7190L01 | Start Date*: 2012-10-03 | ||||||||||||||||
Sponsor Name:ZAMBON S.p.A. | ||||||||||||||||||
Full Title: Evaluation of efficacy and safety of Ibuprofen Arginine 600 mg tid vs. Ibuprofen 600 mg tid in the treatment of pain and inflammation in Osteoarthritis (OA) patients with hypertension pharmacologic... | ||||||||||||||||||
Medical condition: Osteoarthritis of the knee or hip that requires taking NSAIDs for at least 14 days and hypertension stabilized with drugs. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-001197-93 | Sponsor Protocol Number: CG100649-2-01 | Start Date*: 2007-09-21 | ||||||||||||||||
Sponsor Name:CrystalGenomics, Inc. | ||||||||||||||||||
Full Title: Double-blind, placebo controlled Phase II repeat dose study of the safety and efficacy of three parallel loading and maintenance dose regimens of CG100649 versus placebo for the treatment of primar... | ||||||||||||||||||
Medical condition: Primary osteoarthritis (OA) of the knee or hip | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: HU (Completed) DE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000078-21 | Sponsor Protocol Number: HCT 3012-X-303 | Start Date*: 2007-10-11 | |||||||||||
Sponsor Name:NicOx S.A | |||||||||||||
Full Title: A 13-Week, Phase 3, Multicenter, Randomized, Parallel-Group, Double-Blind, Placebo bid and Naproxen 500 mg bid, Controlled Study on the Efficacy on Signs and Symptoms, and Safety of Naproxcinod (HC... | |||||||||||||
Medical condition: Osteoarthritis of the Hip | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) IT (Completed) DE (Completed) BG (Completed) GB (Completed) ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001048-32 | Sponsor Protocol Number: 0701017 | Start Date*: 2008-09-15 | |||||||||||||||||||||||||||||||
Sponsor Name:CHU SAINT-ETIENNE | |||||||||||||||||||||||||||||||||
Full Title: Prospective, multicentre, open-label study evaluating Fondaparinux (1,5 mg/day) in venous thromboembolic events prevention in patients with renal impairment defined by a creatinin clearance between... | |||||||||||||||||||||||||||||||||
Medical condition: Patients with renal impairment defined by a creatinin clearance between 20 and 50 ml/min and undergoing a major orthopaedic surgery (hip fracture, total hip replacement and total knee replacement) | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: FR (Completed) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001702-15 | Sponsor Protocol Number: R475-OA-1688 | Start Date*: 2018-03-05 | ||||||||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | ||||||||||||||||||
Full Title: A Phase 3 Randomized, Double-Blind, Multi-Dose, Placebo And NSAID-Controlled Study To Evaluate The Efficacy And Safety Of Fasinumab In Patients With Pain Due To Osteoarthritis Of The Knee Or Hip | ||||||||||||||||||
Medical condition: Pain due to osteoarthritis of the knee or hip | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) DE (Completed) EE (Completed) GB (GB - no longer in EU/EEA) RO (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-001618-13 | Sponsor Protocol Number: R475-OA-1816 | Start Date*: 2018-11-28 | ||||||||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | ||||||||||||||||||
Full Title: Study to Evaluate Arthroplasty Specimens in the Phase 3 Fasinumab Program for Osteoarthritis of the Knee and Hip | ||||||||||||||||||
Medical condition: Pain due to osteoarthritis of the knee or hip | ||||||||||||||||||
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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: 2009-016445-25 | Sponsor Protocol Number: 2010-KVA | Start Date*: 2010-01-07 | ||||||||||||||||
Sponsor Name:Ortopædkirurgisk Afd. E, Århus Universitetshospital | ||||||||||||||||||
Full Title: Undersøgelse af postoperative bolus infusioner ved primær hoftealloplastik | ||||||||||||||||||
Medical condition: Patienter med hofteartrose der indlægges til primær total hoftealloplastik | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003783-36 | Sponsor Protocol Number: R475-PN-1523 | Start Date*: 2016-05-19 | ||||||||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | ||||||||||||||||||
Full Title: A Phase 3 Randomized, Double-Blind, Multi-Dose, Placebo-Controlled Study to Evaluate the Long-Term Safety and the Efficacy of Fasinumab in Patients with Pain Due to Osteoarthritis of the Knee or Hip | ||||||||||||||||||
Medical condition: Pain due to osteoarthritis of the knee or hip | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BG (Completed) DK (Completed) SE (Completed) DE (Completed) LT (Completed) GB (GB - no longer in EU/EEA) PL (Completed) ES (Completed) HU (Completed) RO (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
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