- Trials with a EudraCT protocol (15)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
15 result(s) found for: Power training.
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EudraCT Number: 2009-011448-20 | Sponsor Protocol Number: 2008.11.007 | Start Date*: 2009-06-22 | |||||||||||
Sponsor Name:Dutch Diabetes Research Foundation | |||||||||||||
Full Title: Hyperoxic exercise training as an innovative therapy to improve metabolic control, endothelial dysfunction and physical fitness in deconditioned type 2 diabetes patients | |||||||||||||
Medical condition: insulin resistance, endothelial dysfunction, cardiovascular fitness, lipid metabolism and glycemic control in deconditioned non-insulin dependent type 2 diabetes patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000335-17 | Sponsor Protocol Number: MPR001 | Start Date*: 2014-10-28 |
Sponsor Name:Research and Development University Hospital of North Staffordshire
[...]
1. Research and Development University Hospital of North Staffordshire
2. Keele University |
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Full Title: The Effect of Rotigotine on Memory in Idiopathic Parkinson's Disease without Cognitive Impairment | ||
Medical condition: Idiopathic Parkinson's Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2013-000906-52 | Sponsor Protocol Number: SC0806-A101 | Start Date*: 2015-03-24 |
Sponsor Name:BioArctic AB | ||
Full Title: An Open, Randomized, Rehabilitation-controlled Study to Assess Safety, Tolerability, and Efficacy of Heparin Activated Recombinant Human Fibroblast Growth Factor 1 on a Biodegradable Device in Subj... | ||
Medical condition: Complete Traumatic Spinal Cord Injury (TSCI) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) NO (Completed) EE (Prematurely Ended) FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-000054-28 | Sponsor Protocol Number: OLIGOTREAT | Start Date*: 2023-06-02 | |||||||||||
Sponsor Name:Klinikum der Universität München | |||||||||||||
Full Title: Combining Clemastine and Aerobic Exercise to Treat Cognitive Dysfunction in Schizophrenia by Targeting Myelin Plasticity (OligoTreat) | |||||||||||||
Medical condition: Schizophrenia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000180-13 | Sponsor Protocol Number: HAT1 | Start Date*: 2015-04-22 |
Sponsor Name:Medisch Centrum Haaglanden | ||
Full Title: The value of a High-Volume Image-Guided Injections (HVIGI) in chronic midportion Achilles tendinopathy: a double-blind, placebo-controlled, randomised clinical trial | ||
Medical condition: Chronic midportion Achilles tendinopathy | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-004140-32 | Sponsor Protocol Number: PRP-MUSCULO-2014-01 | Start Date*: 2014-04-28 | |||||||||||
Sponsor Name:Unidad de Cirugia Artroscópica | |||||||||||||
Full Title: CLINICAL STUDY TO ASSES THERAPEUTIC USE OF PLATELET RICH PLASMA IN ACUTE MUSCLE INJURIES IN ELITE ATHLETES" | |||||||||||||
Medical condition: Acute Muscle Injury Type 3A-3B (Munich classification) or type II (Classification of Otto Chan), confirmed by radiological diagnosis and clinical agreement. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001038-32 | Sponsor Protocol Number: 48-03LXPU | Start Date*: 2019-10-15 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Lead Chemical Company Ltd | ||||||||||||||||||||||||||||||||||||||
Full Title: Randomized, controlled, double-blind, multi-center trial to evaluate the efficacy and safety of a Loxoprofen sodium 60 mg tape medicated plaster vs. placebo in the local symptomatic and short-term ... | ||||||||||||||||||||||||||||||||||||||
Medical condition: Acute blunt, soft tissue injuries of the limbs | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-005217-41 | Sponsor Protocol Number: 51-03FPAEU | Start Date*: 2021-09-06 |
Sponsor Name:Lead Chemical Company Ltd | ||
Full Title: Randomized, controlled, multi-center trial to evaluate the efficacy and safety of a Flurbiprofen 40 mg cutaneous hydrogel medicated plaster vs. placebo and vs. a marketed active comparator in the l... | ||
Medical condition: pain in acute strains, sprains or bruises of the soft tissues following blunt trauma, e.g. sports injuries | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-002131-34 | Sponsor Protocol Number: GS-US-357-1394 | Start Date*: 2015-05-07 | |||||||||||
Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
Full Title: A Phase 2, Dose-Ranging, Randomized, Double-Blind, Placebo-Controlled Study of GS-4997 in Subjects with Pulmonary Arterial Hypertension | |||||||||||||
Medical condition: Men and women, ages 18 through 75 years, with a diagnosis of idiopathic PAH, heritable PAH or PAH associated with connective tissue disease (PAH-CTD), congenital heart defects (repaired), drug and ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) NL (Completed) ES (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000801-64 | Sponsor Protocol Number: BTG001 | Start Date*: 2013-02-09 | |||||||||||
Sponsor Name:University Hospital of North Staffordshire
[...]
1. University Hospital of North Staffordshire
2. Keele University |
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Full Title: A Phase IV Acceptability and Feasibility Trial of the Effects of Medication on Memory in Idiopathic Nondementing Parkinson’s Disease. | |||||||||||||
Medical condition: Idiopathic Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001068-36 | Sponsor Protocol Number: R03465 | Start Date*: 2014-10-22 | |||||||||||
Sponsor Name:Central Manchester University Hospitals NHS Foundation Trust | |||||||||||||
Full Title: Onabotulinum toxin-A versus extended release tolterodine in the management of idiopathic overactive bladder in children: A pilot randomised controlled trial (OVERT) | |||||||||||||
Medical condition: Idiopathic Overactive Bladder | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005003-40 | Sponsor Protocol Number: BTS651/12 | Start Date*: 2013-01-21 |
Sponsor Name:MUCOS Pharma GmbH & Co. KG | ||
Full Title: Effects of Wobenzym® plus in healthy, sportive people after eccentric exercise - a randomized, two-stage, double-blind, placebo-controlled cross-over trial | ||
Medical condition: "Healthy volunteers" Influence of the product on exercise induced muscle damage, noticable in temporal strength loss and muscle soreness. The indication is as defined in the SmPC: Swelling and infl... | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-003543-29 | Sponsor Protocol Number: 48-04LXPU | Start Date*: 2021-05-07 |
Sponsor Name:Lead Chemical Company Ltd. | ||
Full Title: Randomized, controlled, multi-center trial to evaluate the efficacy and safety of a Loxoprofen sodium 60 mg medicated plaster vs. placebo and vs. a marketed comparator in the local symptomatic and ... | ||
Medical condition: Acute blunt, soft tissue injuries of the muscles or limbs | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-005287-21 | Sponsor Protocol Number: Simon1234 | Start Date*: 2023-06-01 | |||||||||||
Sponsor Name:Rigshospitalet, Center for Aktiv Sundhed, section 7641 | |||||||||||||
Full Title: Exercise-induced cardiac adaptions in rheumatoid arthritis patients during interleukin-6 vs. tumor necrosis factor antibody therapy: a randomised controlled study (RABEX). | |||||||||||||
Medical condition: Rheumatoid Athritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005165-14 | Sponsor Protocol Number: TK-254R-0201 | Start Date*: 2021-03-25 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Teikoku Seiyaku Co Ltd. | ||||||||||||||||||||||||||||||||||||||
Full Title: Randomized, controlled, double-blind, multi-center trial to evaluate the | ||||||||||||||||||||||||||||||||||||||
Medical condition: Acute strains, sprains or bruises of the extremities following blunt trauma | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
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