- Trials with a EudraCT protocol (12)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
12 result(s) found for: Joint contracture.
Displaying page 1 of 1.
EudraCT Number: 2006-006143-31 | Sponsor Protocol Number: AUX-CC-854.01 | Start Date*: 2007-10-19 | |||||||||||
Sponsor Name:Auxilium UK Limited | |||||||||||||
Full Title: A Phase 3, Open Label Study of Safety and Efficacy of AA4500 in the Treatment of Subjects With Dupuytren's Contracture | |||||||||||||
Medical condition: Dupuytren's Contracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) FI (Completed) DK (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000673-40 | Sponsor Protocol Number: 1234 | Start Date*: 2015-01-06 |
Sponsor Name:ous | ||
Full Title: Prospective randomized trial between Percutaneous Needle Fasciotomy and Xiapex injection | ||
Medical condition: Dupuytrens contracture of the hand | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-000666-17 | Sponsor Protocol Number: RR37_21_01 | Start Date*: 2022-07-30 | |||||||||||
Sponsor Name:Fidia Farmaceutici Spa | |||||||||||||
Full Title: A Phase II double-blind, randomised, placebo-controlled study of efficacy and safety of Vibrio alginolyticus collagenase administered to patients with Dupuytren contracture | |||||||||||||
Medical condition: Dupuytren contracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005065-21 | Sponsor Protocol Number: AUX-CC-862 | Start Date*: 2012-03-26 | |||||||||||
Sponsor Name:Auxilium UK Limited | |||||||||||||
Full Title: Retreatment of recurrent contractures in joints effectively treated with AA4500 (collagenase clostridium histolyticum [XIAFLEX®/XIAPEX®]) in an Auxilium-sponsored Phase 3 Study in the United States... | |||||||||||||
Medical condition: Dupuytren's contracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004251-76 | Sponsor Protocol Number: 87230 | Start Date*: 2017-05-22 | ||||||||||||||||
Sponsor Name:University Hospitals of Leicester NHS Trust | ||||||||||||||||||
Full Title: A pragmatic multi-centre randomised controlled non-inferiority, cost effectiveness trial comparing injections of collagenase into the cord to surgical correction in the treatment of moderate Dupuyt... | ||||||||||||||||||
Medical condition: Dupuytren's contracture | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001780-40 | Sponsor Protocol Number: 11069 | Start Date*: 2015-05-21 | |||||||||||
Sponsor Name:University of Oxford, Clinical Trials and Research Governance | |||||||||||||
Full Title: A multi-centre, double blind, randomised, placebo-controlled, parallel group, phase II trial to determine the efficacy of intra-nodular injection of anti-TNF to control disease progression in early... | |||||||||||||
Medical condition: Dupuytren's disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004091-19 | Sponsor Protocol Number: AUX-CC-867 | Start Date*: 2012-12-28 | |||||||||||
Sponsor Name:Auxilium UK Limited | |||||||||||||
Full Title: A Phase 3b open-label, historically-controlled study to assess the safety and efficacy of two concurrent injections of AA4500 in adult subjects with multiple Dupuytren’s contractures with palpable ... | |||||||||||||
Medical condition: Dupuytren's contracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) GB (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000494-67 | Sponsor Protocol Number: 1.2 | Start Date*: 2013-10-22 | |||||||||||
Sponsor Name:Klinik for håndkirurgi, Gentofte hospital | |||||||||||||
Full Title: Needle fasciotomi vs collagenase for treatment of Dupuytrens contracture in 2nd, 3rd, 4th and 5th metacarpophalangeal joint. | |||||||||||||
Medical condition: Dupuytrens contracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019888-10 | Sponsor Protocol Number: B1531002 | Start Date*: 2010-11-10 | |||||||||||
Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: PROSPECTIVE OPEN-LABEL INVESTIGATION OF THE NON-SURGICAL TREATMENT WITH COLLAGENASE CLOSTRIDIUM HISTOLYTICUM (XIAPEX®) | |||||||||||||
Medical condition: Dupuytren’s contracture | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) HU (Completed) ES (Completed) SE (Completed) DK (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001221-13 | Sponsor Protocol Number: 2639063 | Start Date*: 2013-10-10 | |||||||||||
Sponsor Name:Akershus university hospital | |||||||||||||
Full Title: Dupytren’s disease study A randomized controlled trial comparing clostridium histolyticum with needle aponeurotomy. | |||||||||||||
Medical condition: Dupytren’s disease, primary MCP joint contractures of the third, forth and fifth finger of the hand. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005742-42 | Sponsor Protocol Number: SCALA | Start Date*: 2023-04-13 | |||||||||||
Sponsor Name:Groupement de Coopération Sanitaire Ramsay Générale de Santé pour l’Enseignement et la Recherche | |||||||||||||
Full Title: Effect of botulinum toxin on hamstring contracture and the occurrence of cyclops syndrome after anterior cruciate ligament reconstruction | |||||||||||||
Medical condition: Cyclops syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-006271-42 | Sponsor Protocol Number: HZNP-HZN-825-302 | Start Date*: 2022-12-15 | |||||||||||
Sponsor Name:Horizon Therapeutics Ireland DAC | |||||||||||||
Full Title: A Multicenter, Open-label Extension Trial to Evaluate the Efficacy, Safety and Tolerability of HZN-825 in Patients with Diffuse Cutaneous Systemic Sclerosis | |||||||||||||
Medical condition: Diffuse Cutaneous Systemic Sclerosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) GR (Trial now transitioned) IT (Trial now transitioned) DE (Trial now transitioned) AT (Trial now transitioned) ES (Ongoing) PL (Trial now transitioned) PT (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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