- Trials with a EudraCT protocol (286)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
286 result(s) found for: Physical exercise.
Displaying page 1 of 15.
EudraCT Number: 2016-000573-20 | Sponsor Protocol Number: 1.0 | Start Date*: 2016-06-14 |
Sponsor Name:Department of Sports Medicine, Institute for Sport Sciences, Justu-Liebig-University of Gießen | ||
Full Title: Effects of MUTAFLOR® on exercise-induced gastro-intestinal dysfunction | ||
Medical condition: To investigate the effects of Mutaflor® Suspension on exercise induced gastrointestinal symptoms for 3 hours after a strenous exercise test on a treadmill | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
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: 2016-002435-15 | Sponsor Protocol Number: FiHM003 | Start Date*: 2017-08-10 |
Sponsor Name:Fundación de Investigación HM Hospitales | ||
Full Title: Pilot study to assess physical exercise intervention in neoadjuvant treatment with nab-paclitaxel in patients with triple negative breast cancer | ||
Medical condition: Supervised exercise regimen given during neoadjuvant chemotherapy for triple negative breast cancer patients. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-002987-26 | Sponsor Protocol Number: KOLterbutaline | Start Date*: 2011-08-24 |
Sponsor Name:Bispebjerg Hospital | ||
Full Title: Effects of high dose terbutaline on physical performance in patients with chronic obstructive pulmonary disease and acute inflammatory response after exercise | ||
Medical condition: To investigate the effects of terbutaline on repeated exercise performance in patients with chronic obstructive pulmonary disease (COPD). Furthermore to examine the inflammatory response during and... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-004503-13 | Sponsor Protocol Number: KOLprednisolone | Start Date*: 2012-12-12 |
Sponsor Name:Bispebjerg Hospital | ||
Full Title: Effect of Glococorticosteroids on physical performance in patients with chronic obstructive pulmonary disease and acute inflammatory response after exercise | ||
Medical condition: To investigate the effects of prednisone and Solu-Medrol on physical performance in patients with chronic obstructive pulmonary disease(COPD). Furthermore to examine the inflammatory response durin... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-002804-42 | Sponsor Protocol Number: Beta2-Mikro | Start Date*: 2012-09-10 |
Sponsor Name:Bispebjerg Hospital | ||
Full Title: The effects of high dose beta2-agonists on physical performance in healthy male subjects | ||
Medical condition: No medical condition will be investigated. To examine the effects of beta2-agonists on aerobic and anaerobic exercise performance. | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: Removed from public view |
EudraCT Number: 2019-003209-89 | Sponsor Protocol Number: ULTRAFLEXI1 | Start Date*: 2019-12-12 | |||||||||||
Sponsor Name:Medical University of Graz | |||||||||||||
Full Title: A trial investigating ultra-long-acting basal insulins’ flexibility around multiple spontaneous exercise sessions in people with type 1 diabetes: a head to head comparison of 2nd generation insulin... | |||||||||||||
Medical condition: Type 1 Diabetes | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004257-26 | Sponsor Protocol Number: 160350 | Start Date*: 2005-02-28 |
Sponsor Name:Organisation name was not entered | ||
Full Title: A randomised study of the effect of metformin and exercise in overweight women with polycystic ovary syndrome | ||
Medical condition: Polycystic ovary syndrome is a condition characterized by obesity, anovulation and hyperandrogenism/hyperandrogenemia. Insulin resistance is common, and treatment is aimed at reducing this. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003501-15 | Sponsor Protocol Number: 408-C-1403 | Start Date*: 2015-03-05 | |||||||||||
Sponsor Name:Reata Pharmaceuticals, Inc. | |||||||||||||
Full Title: A PHASE 2 STUDY OF THE SAFETY, EFFICACY, AND PHARMACODYNAMICS OF RTA 408 IN THE TREATMENT OF MITOCHONDRIAL MYOPATHY | |||||||||||||
Medical condition: Mitochondrial myopathy as evidenced by the following 2 criteria (must meet both): a. Have a history of exercise intolerance with or without weakness and/or progressive exercise intolerance (in whi... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000461-28 | Sponsor Protocol Number: Resubmission A | Start Date*: 2008-06-10 | ||||||||||||||||
Sponsor Name:Karolinska institutet | ||||||||||||||||||
Full Title: Effect of exercise or metformin on nocturnal blood pressure and other risk factors for cardiovascular heart disease among obese adolescents | ||||||||||||||||||
Medical condition: The aim is to, among obese adolescents study impact of exercise or metformin therapy on nocturnal blood pressure and related cardiovascular disease risk factors (e.g. insulin sensitivity, IMT, LVM,... | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012621-12 | Sponsor Protocol Number: R&D2008GR03 | Start Date*: 2009-08-06 | |||||||||||
Sponsor Name:University of Dundee | |||||||||||||
Full Title: Maximising physical function in later life: a 2 centre randomised trial of progressive resistance exercise training in combination with ACE inhibition | |||||||||||||
Medical condition: Age related decline in muscle function (sarcopenia) | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004631-77 | Sponsor Protocol Number: EX21102013 | Start Date*: 2014-01-24 |
Sponsor Name:Medizinische Universität Graz/Endokrinologie und Stoffwechsel | ||
Full Title: Exercise and Blood Glucose Levels in Patients with Type I Diabetes - a Pilot Study | ||
Medical condition: Type 1 diabetes | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
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: 2018-004393-10 | Sponsor Protocol Number: GN18CA068 | Start Date*: 2019-07-17 | |||||||||||
Sponsor Name:NHS Greater Glasgow & Clyde [...] | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, cross-over trial of zibotentan in microvascular angina | |||||||||||||
Medical condition: Microvascular Angina and impaired exercise intolerance. | |||||||||||||
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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: 2023-000150-20 | Sponsor Protocol Number: 1 | Start Date*: 2023-03-22 |
Sponsor Name:Bispebjerg-Frederiksberg Hospital | ||
Full Title: The effect of exercise on pharmacodynamics and pharmacokinetics of a single dose of unfractionated heparin: A randomized, controlled, cross-over study | ||
Medical condition: Unfractionated heparin is used for the prevention and treatment of deep vein thrombosis and complications hereof | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-001278-24 | Sponsor Protocol Number: MEIN/10/Ran-Cad/003 | Start Date*: 2011-09-02 | |||||||||||
Sponsor Name:Menarini International Operations Luxembourg SA | |||||||||||||
Full Title: EFFICACY OF RANOLAZINE IN PATIENTS WITH CORONARY ARTERY DISEASE (CAD) | |||||||||||||
Medical condition: Excercise angina in patients with Coronary Artery Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Completed) ES (Completed) IE (Prematurely Ended) GB (Prematurely Ended) DE (Prematurely Ended) AT (Prematurely Ended) IT (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001516-11 | Sponsor Protocol Number: 201832 | Start Date*: 2017-07-10 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: 201832: A Randomised, Double-Blind, Double-Dummy, Crossover Comparison of Fluticasone Furoate/Vilanterol 100/25 mcg Once Daily Versus Fluticasone Propionate 250 mcg Twice Daily in Adolescent and Ad... | |||||||||||||
Medical condition: Adolescent and Adult Subjects with Asthma and Exercise-Induced Bronchoconstriction | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004122-18 | Sponsor Protocol Number: 2012GR12 | Start Date*: 2014-12-12 | |||||||||||
Sponsor Name:University of Dundee, Tayside Clinical Trials Unit | |||||||||||||
Full Title: A Prospective Study to Evaluate the Effect of Allopurinol on Muscle Energetics in Older People with Impaired Physical Function. | |||||||||||||
Medical condition: FUNCTIONAL IMPAIRMENT | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005179-32 | Sponsor Protocol Number: GRMSS-04-07 | Start Date*: 2008-09-15 |
Sponsor Name:Joint Stock Company "Grindeks" | ||
Full Title: Mildronate - Efficacy And Safety Of Treatment For Chronic Coronary Heart Disease (Stable Angina) I | ||
Medical condition: Chronic coronary heart disease (stable angina) | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: LV (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-000144-25 | Sponsor Protocol Number: 234820 | Start Date*: 2019-03-08 | ||||||||||||||||
Sponsor Name:King's College Hospital NHS Foundation Trust | ||||||||||||||||||
Full Title: Multicentre prospective double blinded randomised controlled trial of the effect of intravenous iron supplementation and exercise training in Iron deficient, but not anaemic, patients with Chronic ... | ||||||||||||||||||
Medical condition: Iron deficiency in stage 3-4 CKD | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: View results |
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