- Trials with a EudraCT protocol (38)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
38 result(s) found for: Capsule of the hip joint.
Displaying page 1 of 2.
EudraCT Number: 2009-015383-33 | Sponsor Protocol Number: Eto-Dic-01 | Start Date*: 2010-08-30 | |||||||||||
Sponsor Name:Freistaat Bayern, vertreten durch die Universität Regensburg | |||||||||||||
Full Title: Die perioperative Anwendung von Etoricoxib verglichen mit Diclofenac bei Patienten nach Implantation einer Hüftgelenkstotalendoprothese, prospektive, doppelt blinde Phase IIIb Studie | |||||||||||||
Medical condition: In this clinical trial we will investigate patients who suffer from primary or secondary coxarthrosis where an implantation of a total hip joint endoprosthesis is indicated. It will be analyzed whe... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002239-16 | Sponsor Protocol Number: SM2-KHT-2015 | Start Date*: 2015-08-12 | ||||||||||||||||
Sponsor Name:Næstved Hospital | ||||||||||||||||||
Full Title: PANSAID – PAracetamol and NSAID in combination: A randomised, blinded, parallel 4-group clinical trial | ||||||||||||||||||
Medical condition: Pain after total hip replacement surgery | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
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: 2005-001791-13 | Sponsor Protocol Number: OXY4009 | Start Date*: 2005-08-31 | |||||||||||
Sponsor Name:Mundipharma GmbH | |||||||||||||
Full Title: An open-label, randomized, parallel-group, monocenter study to evaluate safety and efficacy of Oxycodone Hydrochloride administered orally (CR) and intravenously in patients with total hip endopros... | |||||||||||||
Medical condition: Male and female patients who are designated for a total hip endoprosthesis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
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: 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: 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: 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: 2005-004527-19 | Sponsor Protocol Number: LAL1 | Start Date*: 2006-01-30 |
Sponsor Name:MRC Health Services Research Collaboration | ||
Full Title: Joint pain personalised treatment assessment to investigate the acceptability of modified release oxycontin for managing chronic pain in patients with osteoarthritis of the hip | ||
Medical condition: Hip Osteoarthritis | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-002549-12 | Sponsor Protocol Number: A4091064 | Start Date*: 2015-09-08 | ||||||||||||||||
Sponsor Name:Pfizer Inc, 235 East 42nd Street, New York, NY 10017 | ||||||||||||||||||
Full Title: A PHASE 3, MULTICENTER, LONG-TERM OBSERVATIONAL STUDY OF SUBJECTS FROM TANEZUMAB STUDIES WHO UNDERGO A TOTAL KNEE, HIP OR SHOULDER REPLACEMENT | ||||||||||||||||||
Medical condition: Osteoarthritis of the hip or knee | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) AT (Completed) ES (Completed) BG (Completed) DE (Completed) PT (Completed) FI (Completed) GB (Completed) SE (Completed) LT (Completed) HR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-002772-14 | Sponsor Protocol Number: COX189A2367 | Start Date*: 2005-11-10 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A 13-week, multicenter, randomized, double-blind, doubledummy, placebo-controlled, parallel group trial of lumiracoxib (COX189) 100 mg o.d. in patients with primary hip osteoarthritis using celecox... | |||||||||||||
Medical condition: Primary osteoarthritis of the hip | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003721-22 | Sponsor Protocol Number: A4091058 | Start Date*: 2016-01-14 | ||||||||||||||||
Sponsor Name:Pfizer Inc, 235 East 42nd Street, New York, NY 10017 | ||||||||||||||||||
Full Title: A PHASE 3 RANDOMIZED, DOUBLE-BLIND, ACTIVE-CONTROLLED, MULTICENTER STUDY OF THE LONG-TERM SAFETY AND EFFICACY OF SUBCUTANEOUS ADMINISTRATION OF TANEZUMAB IN SUBJECTS WITH OSTEOARTHRITIS OF THE HIP ... | ||||||||||||||||||
Medical condition: Osteoarthritis of the hip or knee | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BG (Completed) SK (Completed) LT (Completed) HR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-000089-12 | Sponsor Protocol Number: HIP/FUSION#4 | Start Date*: 2018-04-24 | |||||||||||
Sponsor Name:Institut for Klinisk Medicin, Aarhus Universitet | |||||||||||||
Full Title: Effect and safety of the iliopsoas plane block in healthy volunteers | |||||||||||||
Medical condition: No specific medical condition is investigated. The objective of the trial is to investigate a method for postoperative analgesia after elective hip surgery. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-005020-29 | Sponsor Protocol Number: R475-OA-1611 | Start Date*: 2018-04-10 | ||||||||||||||||
Sponsor Name:Regeneron Pharmaceuticals, Inc. | ||||||||||||||||||
Full Title: A Phase 3 Randomized, Double-blind, Multi-dose, Placebo and Naproxen-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: BG (Completed) LT (Completed) GB (GB - no longer in EU/EEA) DK (Completed) PL (Completed) HU (Completed) ES (Ongoing) RO (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-004013-41 | Sponsor Protocol Number: AUH-TFB-SSPS-3 | Start Date*: 2015-09-18 | ||||||||||||||||
Sponsor Name:Thomas Fichnter Bendtsen | ||||||||||||||||||
Full Title: Supra Sacral Parallel Shift - ultrasound/MR image fusion guided lumbosacral plexus block | ||||||||||||||||||
Medical condition: | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
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: 2004-000979-33 | Sponsor Protocol Number: ITAES PR 2503 | Start Date*: 2005-01-31 | |||||||||||
Sponsor Name:LABORATOIRES EXPANSCIENCE | |||||||||||||
Full Title: A multinational multicentre randomised paralle group study on therapeutic efficacy and tolerability of PIASCLEDINE capsules 300 mg in comparison with placebo in the treatment of hip osteoarthritis | |||||||||||||
Medical condition: hip osteoarthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005544-33 | Sponsor Protocol Number: AUH-TFB-SR-ULMR | Start Date*: 2016-02-08 | ||||||||||||||||
Sponsor Name:Thomas Fichtner Bendtsen | ||||||||||||||||||
Full Title: Shamrock – Ultrasound/MR image fusion guided lumbar plexus blocks | ||||||||||||||||||
Medical condition: Hip surgery anaesthesia and perioperative analgesia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-003444-80 | Sponsor Protocol Number: 2020-01471 | Start Date*: 2020-11-17 |
Sponsor Name:Sahlgrenska University Hospital | ||
Full Title: Evaluation of the clinical implementation of biofilm susceptibility to antibiotics using Minimum Biofilm Eradication Concentration (MBEC) in addition to Minimum Inhibitory Concentration (MIC) to gu... | ||
Medical condition: Periprosthetic hip or knee joint infections | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2022-004192-16 | Sponsor Protocol Number: 3.0 | Start Date*: 2023-04-12 | ||||||||||||||||
Sponsor Name:idival | ||||||||||||||||||
Full Title: Evaluation of the efficacy of treatment with mucosal bacterial vaccines (autovaccines) versus suppressive antibiotic treatment in subjects with hip or knee prosthesis infections. | ||||||||||||||||||
Medical condition: Patients with chronic infections of hip and knee prostheses, without the possibility of curative treatment of the infection. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
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