- Trials with a EudraCT protocol (13)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
13 result(s) found for: Stair climbing.
Displaying page 1 of 1.
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: 2007-000982-38 | Sponsor Protocol Number: 06/JM/119 | Start Date*: 2007-06-14 |
Sponsor Name:Greenpark Health Care Trust | ||
Full Title: Pain and mobility outcomes following patient controlled lumbar plexus block for primary joint arthroplasty | ||
Medical condition: Pain control after primary joint arthroplasty | ||
Disease: | ||
Population Age: | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2013-001152-35 | Sponsor Protocol Number: UX003-CL201 | Start Date*: 2013-08-02 |
Sponsor Name:Ultragenyx Pharmaceutical Inc. | ||
Full Title: An Open-Label Phase 1/2 Study to Assess the Safety, Efficacy and Dose of UX003 rhGUS Enzyme Replacement Therapy in Patients with MPS 7 | ||
Medical condition: Mucopolysaccharidosis type 7 (MPS 7, Sly syndrome) | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-006062-40 | Sponsor Protocol Number: I1Q-MC-JDDJ | Start Date*: 2012-06-04 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Phase 2 Randomized Study to Investigate the Efficacy and Safety of LY2495655 Versus Placebo in Older Patients Who Have Fallen Recently and Have Muscle Weakness | |||||||||||||
Medical condition: Disuse atrophy | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002383-95 | Sponsor Protocol Number: 0773-005-00 | Start Date*: 2007-08-08 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: A Phase IIa Randomized, Placebo-Controlled Clinical Trial to Study the Efficacy and Safety of MK-0773 in Patients with Sarcopenia | |||||||||||||
Medical condition: Sarcopenia | |||||||||||||
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Population Age: Elderly | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) ES (Completed) FR (Completed) GB (Completed) FI (Completed) SE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002509-22 | Sponsor Protocol Number: 0677-032 | Start Date*: 2005-09-01 | |||||||||||
Sponsor Name:Merck Sharp & Dohme (Sweden) AB | |||||||||||||
Full Title: A 24-Week, Double-Blind, Randomized, Placebo-Controlled, Multicenter Study to Assess the Safety and Efficacy of MK-0677 for the Treatment of Sarcopenia in Patients Recovering From Hip Fracture | |||||||||||||
Medical condition: Sarcopenia | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) GB (Prematurely Ended) DE (Prematurely Ended) ES (Prematurely Ended) DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000405-27 | Sponsor Protocol Number: 05JM128 | Start Date*: 2006-06-01 |
Sponsor Name:Greenpark Health Care Trust | ||
Full Title: Postoperative pain and mobility outcomes after primary hip and knee arthroplasty. A comparison of intravenous morphine with local wound infiltration. | ||
Medical condition: Osteoarthritis of the hip and knee joints | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2019-000809-71 | Sponsor Protocol Number: APPI2-PT-2019-01 | Start Date*: 2019-06-18 | |||||||||||
Sponsor Name:The Parker Institute, Bispebjerg and Frederiksberg Hospital, The Capital Region of Denmark | |||||||||||||
Full Title: Direct comparison of intra-articular saline injections with an education plus exercise program for treatment of knee osteoarthritis symptoms: A randomised, open label, controlled, evidence based trial | |||||||||||||
Medical condition: Knee osteoarthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001008-13 | Sponsor Protocol Number: 497 | Start Date*: 2013-09-18 |
Sponsor Name:Sint Maartenskliniek | ||
Full Title: Fast-track rehabilitation protocol for Total Knee Arthroplasty: A Randomized Controlled Trial comparing Local Infiltration Analgesia with Femoral Nerve Block | ||
Medical condition: patients requiring total knee arthroplasty for non-inflammatory osteoarthritis of the knee | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-003139-39 | Sponsor Protocol Number: JAN12006-09 | Start Date*: 2017-05-16 |
Sponsor Name:Spherium Biomed | ||
Full Title: Double-blind, randomized, placebo-controlled, Single-center, Exploratory Clinical Trial to Investigate Safety and Efficacy of COMBOPROFEN for treatment of muscular pain associated with DOMS | ||
Medical condition: Delayed onset muscular soreness | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001223-49 | Sponsor Protocol Number: PTC124-GD-041DMD | Start Date*: 2018-01-16 | |||||||||||
Sponsor Name:PTC Therapeutics, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Efficacy and Safety Study of Ataluren in Patients with Nonsense Mutation Duchenne Muscular Dystrophy and Open-Label Extension | |||||||||||||
Medical condition: Nonsense Mutation Duchenne Muscular Dystrophy | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male | ||||||||||||
Trial protocol: BG (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022486-10 | Sponsor Protocol Number: MT-102-2001 | Start Date*: 2010-11-02 | |||||||||||
Sponsor Name:Myotec Therapeutics Limited | |||||||||||||
Full Title: A multicentre, randomised, double-blind, placebo-controlled, dose-finding phase II study to evaluate the efficacy of two different doses of MT-102 administered over a sixteen week period in subject... | |||||||||||||
Medical condition: Cachexia related to stage III and IV non-small cell lung cancer and colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) ES (Ongoing) DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000426-29 | Sponsor Protocol Number: I1Q-MC-JDDE | Start Date*: 2011-09-06 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Phase 2 Randomized Study to Investigate the Efficacy and Safety of LY2495655 Versus Placebo in Older Patients Undergoing Elective Total Hip Arthroplasty (eTHA) | |||||||||||||
Medical condition: Disuse atrophy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) DK (Completed) EE (Completed) ES (Completed) SE (Completed) AT (Completed) BE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
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