- Trials with a EudraCT protocol (14)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
14 result(s) found for: Knee Injuries.
Displaying page 1 of 1.
EudraCT Number: 2007-002653-23 | Sponsor Protocol Number: 1/07 | Start Date*: 2008-09-02 | |||||||||||
Sponsor Name:The Police Rehabilitation Centre, Flint House | |||||||||||||
Full Title: A pilot for a case control study to evaluate the effects of High Dosage Oxygen Therapy as an adjunct to an established program of physiotherapy and rehabilitation for sub acute soft tissue knee con... | |||||||||||||
Medical condition: Sub acute soft tissue injuries to the knee . | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000784-16 | Sponsor Protocol Number: NCPACI | Start Date*: 2016-04-15 |
Sponsor Name:Akershus University Hospital | ||
Full Title: Focal cartilage defects in the knee – A randomized controlled trial comparing Autologous Chondrocyte Implantation with arthroscopic debridement | ||
Medical condition: Symptomatic focal cartilage defects in the knee | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-003408-21 | Sponsor Protocol Number: THO-IM_02-CT | Start Date*: 2015-12-09 | |||||||||||
Sponsor Name:Thrombotargets Europe | |||||||||||||
Full Title: A Phase II/III, randomized, controlled, single blind study to evaluate the haemostatic efficacy and safety of topically applied TT-173 in patients undergoing knee arthroplasty | |||||||||||||
Medical condition: Haemostatic effect in patients undergoing knee arthroplasty | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001431-31 | Sponsor Protocol Number: EMR700692-007 | Start Date*: 2013-05-02 | |||||||||||
Sponsor Name:Merck KGaA | |||||||||||||
Full Title: A multicenter, randomized, double-blind, placebo-controlled, parallel-group, Phase II trial to investigate the efficacy and safety of 30 mcg and 100 mcg AS902330 given as one cycle of three intra-a... | |||||||||||||
Medical condition: Knee Cartilage Injury | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
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: 2004-000909-22 | Sponsor Protocol Number: MDS-KET-2004-01 | Start Date*: 2004-08-27 |
Sponsor Name:MDS Pharma Services | ||
Full Title: Comparative efficacy and tolerability of a topical ketoprofen TDS patch vs ketoprofen gel in the treatment of acute pain in soft-tissue injuries | ||
Medical condition: Acute pain in soft-tissue injuries of lower limbs, except toes | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002963-92 | Sponsor Protocol Number: CLRX712A12201 | Start Date*: 2020-02-05 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A randomized, placebo-controlled, subject and investigator blinded study investigating the safety, tolerability and preliminary efficacy of 8-week treatment with intra-articular LRX712 to regenerat... | |||||||||||||
Medical condition: Cartilage injuries | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003418-28 | Sponsor Protocol Number: CLNA043X2201 | Start Date*: 2017-04-18 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A randomized, placebo-controlled, patient and investigator blinded, single dose, Proof of Concept study investigating the safety, tolerability and preliminary efficacy of intra-articular LNA043 in ... | |||||||||||||
Medical condition: Acute cartilage injuries | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015532-14 | Sponsor Protocol Number: EMR700692-003 | Start Date*: 2010-01-22 | |||||||||||
Sponsor Name:Merck Serono S.A. - Geneva | |||||||||||||
Full Title: A multicenter, randomized, double-blind, placebo-controlled, parallel-group phase II trial to investigate the efficacy and safety of weekly intra-articular (i.a.) injections of 10, 30, and 100 µg o... | |||||||||||||
Medical condition: Knee Cartilage Injury | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) SI (Completed) BG (Prematurely Ended) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004613-10 | Sponsor Protocol Number: IRIVITC2008 | Start Date*: 2008-09-12 | ||||||||||||||||
Sponsor Name:University College Hospital Galway | ||||||||||||||||||
Full Title: The role of the antioxidants ascorbic acid and n-acetylcysteine in the attenuation of ischaemia reperfusion injury in a human model | ||||||||||||||||||
Medical condition: Ischaemia reperfusion injury | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: IE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
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: 2011-006270-13 | Sponsor Protocol Number: XCEL-MEN-01 | Start Date*: 2013-01-08 | |||||||||||
Sponsor Name:Banc de Sang i Teixits | |||||||||||||
Full Title: A phase I-IIa safety and efficacy pilot clinical trial of intraarticular administration of autologous mesenchymal stem cells in meniscus injury | |||||||||||||
Medical condition: Degenerative meniscal lesion | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
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: 2006-005802-29 | Sponsor Protocol Number: RD/505/06 | Start Date*: 2007-06-26 | ||||||||||||||||||||||||||
Sponsor Name:Gwent Healthcare NHS Trust | ||||||||||||||||||||||||||||
Full Title: Postoperative analgesia for Total knee replacement: A comparision between intrathecal morphine and peripheral nerve block. | ||||||||||||||||||||||||||||
Medical condition: Postoperative analgesia for Total Knee Replacement | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
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