- Trials with a EudraCT protocol (36)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
36 result(s) found for: Cycling.
Displaying page 1 of 2.
EudraCT Number: 2018-000388-10 | Sponsor Protocol Number: WADA_17C09 | Start Date*: 2019-06-11 |
Sponsor Name:Daniel Sanabria | ||
Full Title: Clinical trial on the effects of the tramadol and paracetamol on physical, cognitive and brain performance during cycling | ||
Medical condition: Sports doping | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-005056-96 | Sponsor Protocol Number: TRAWADA2015 | Start Date*: 2016-05-31 | |||||||||||
Sponsor Name:Daniel Sanabria Lucena | |||||||||||||
Full Title: Use of tramadol in healthy volunteers. Effects on physical performance and sustained attention in cycling. | |||||||||||||
Medical condition: Sport doping | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
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: 2012-000592-17 | Sponsor Protocol Number: MODY-TREAT | Start Date*: 2012-08-03 | |||||||||||
Sponsor Name:Signe H. Østoft, Diabetes Research Division | |||||||||||||
Full Title: The effects of GLP-1 in Maturity- onset diabetes of the young (MODY) | |||||||||||||
Medical condition: 'Maturity onset diabetes of the young', also called 'Hepatocyte nuclear factor 1-alfa daiabetes'. It is a monogenic form of inherited diabetes. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001714-14 | Sponsor Protocol Number: 136PO15274 | Start Date*: 2018-08-17 | |||||||||||
Sponsor Name:AZIENDE CHIMICHE RIUNITE ANGELINI FRANCESCO A.C.R.A.F. S.P.A. | |||||||||||||
Full Title: Clinical evaluation of switching to Lithiofor® (Lithium Sulphate Slow –Release, Li-SR tablets) from Carbolithium® (Lithium Carbonate Immediate-Release, Li-IR, capsules) in Bipolar patients, poorly ... | |||||||||||||
Medical condition: Bipolar disorder I or II with or without rapid cycling | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019778-34 | Sponsor Protocol Number: D1050292 | Start Date*: 2011-03-14 | |||||||||||
Sponsor Name:Sunovion, Inc. | |||||||||||||
Full Title: A RANDOMIZED, 6-WEEK, DOUBLE-BLIND, PLACEBO-CONTROLLED, FLEXIBLE-DOSE, PARALLEL-GROUP STUDY OF LURASIDONE ADJUNCTIVE TO LITHIUM OR DIVALPROEX FOR THE TREATMENT OF BIPOLAR I DEPRESSION IN SUBJECTS ... | |||||||||||||
Medical condition: Bipolar disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) LT (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007457-13 | Sponsor Protocol Number: D1050236 | Start Date*: 2009-10-21 | |||||||||||
Sponsor Name:Sunovion Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, 6-Week, Double-Blind, Placebo-controlled, Fixed-Flexible-Dose, Parallel-Group Study of Lurasidone in the Treatment of Bipolar I Depression | |||||||||||||
Medical condition: Bipolar depression | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007482-23 | Sponsor Protocol Number: D1050235 | Start Date*: 2009-10-21 | |||||||||||
Sponsor Name:Sunovion Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, 6-Week, Double-Blind, Placebo-Controlled, Flexible-Dose, Parallel-Group Study of Lurasidone Adjunctive to Lithium or Divalproex for the Treatment of Bipolar I Depression | |||||||||||||
Medical condition: Bipolar depression | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000113-18 | Sponsor Protocol Number: CLIC477D2302 | Start Date*: 2004-09-23 |
Sponsor Name:Novartis Farmacéutica, S.A. | ||
Full Title: A randomized, double-blind, placebo-controlled, multicenter study to evaluate the efficacy, safety and tolerability of licarbazepine 750-2500 mg/d combined with risperidone in the treatment of mani... | ||
Medical condition: Bipolar I disorder, manic and mixed episodes | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) HU (Completed) FI (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2017-003124-73 | Sponsor Protocol Number: na | Start Date*: 2018-01-31 |
Sponsor Name:Maastricht University | ||
Full Title: Carnitine supplementation as a therapy to improve insulin sensitivity in Type 2 diabetic patients with low carnitine status | ||
Medical condition: Glucose tolerance | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000810-31 | Sponsor Protocol Number: na | Start Date*: 2016-07-08 |
Sponsor Name:Maastricht University | ||
Full Title: Impact of L-Carnitine infusion on Lipid induced Insulin resistance | ||
Medical condition: Glucose tolerance | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004357-94 | Sponsor Protocol Number: NPS-2005-1 | Start Date*: 2006-01-20 |
Sponsor Name:Nordfjord Psychiatric Centre | ||
Full Title: Escitalopram in bipolar depression: a placebo-controlled study of acute and maintenance treatment. | ||
Medical condition: Patients with bipolar disorder in a depressive episode are randomised to receive escitalopram or placebo for eight weeks. Responders to escitalopram are re-randomised to placebo or escitalopram for... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-019802-17 | Sponsor Protocol Number: 205.438 | Start Date*: 2010-09-13 |
Sponsor Name:Boehringer Ingelheim France | ||
Full Title: A randomised, double-blind, placebo-controlled parallel-group trial to confirm the efficacy after 12 weeks and the safety of tiotropium 5 μg administered once daily via the Respimat® device in pati... | ||
Medical condition: Cystic Fibrosis | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: PT (Completed) HU (Completed) FR (Completed) SK (Completed) DE (Completed) GB (Completed) BE (Completed) CZ (Completed) IT (Completed) AT (Completed) IE (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-004903-37 | Sponsor Protocol Number: D1050326 | Start Date*: 2014-07-30 | |||||||||||
Sponsor Name:SUNOVION PHARMACEUTICALS INC. | |||||||||||||
Full Title: A RANDOMIZED, 6-WEEK, DOUBLE-BLIND, PLACEBO-CONTROLLED, FLEXIBLE DOSE, PARALLEL-GROUP STUDY TO EVALUATE THE EFFICACY AND SAFETY OF LURASIDONE IN CHILDREN AND ADOLESCENT SUBJECTS WITH BIPOLAR I DEPR... | |||||||||||||
Medical condition: Bipolar I depression | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Not Authorised) BG (Completed) Outside EU/EEA HU (Completed) DE (Ongoing) GB (Completed) FR (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000114-40 | Sponsor Protocol Number: CLIC477D2303 | Start Date*: 2004-11-19 |
Sponsor Name:Novartis Pharma AG | ||
Full Title: A randomized, double-blind, placebo-controlled, multicenter study to evaluate the efficacy, safety and tolerability of licarbazepine 750-2500 mg/d combined with lithium or valproate in the treatmen... | ||
Medical condition: Bipolar I disorder, manic and mixed episodes DSM-IV criteria 296.0, 296.4 or 296.6 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) SK (Prematurely Ended) CZ (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2021-002126-24 | Sponsor Protocol Number: SEP380-301 | Start Date*: 2022-02-02 | |||||||||||
Sponsor Name:Sunovion Pharmaceuticals Inc. | |||||||||||||
Full Title: A Multi-region, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study Evaluating SEP-4199 Controlled Release (CR) for the Treatment of Major Depressive Episode Associated ... | |||||||||||||
Medical condition: Major Depressive Episode Associated with Bipolar I Disorder | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Prematurely Ended) SK (Prematurely Ended) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006595-11 | Sponsor Protocol Number: 07EU/Prg06 | Start Date*: 2008-09-25 | |||||||||||
Sponsor Name:IBSA Institut Biochimique SA | |||||||||||||
Full Title: Efficacy and Tolerability of Subcutaneous Progesterone (IBSA) versus Vaginal Progesterone Gel (Crinone) for Luteal Phase Support in Patients Undergoing In-Vitro Fertilization (IVF). | |||||||||||||
Medical condition: Patient undergoing in-Vitro Fertilization (IVF) | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001482-17 | Sponsor Protocol Number: F1D-MC-HGKQ(b) | Start Date*: 2004-10-15 |
Sponsor Name:Eli Lilly and Company | ||
Full Title: Olanzapine Versus Divalproex and Placebo in the Treatment of Mild to Moderate Mania Associated with Bipolar I disorder. | ||
Medical condition: Manic or Mixed Episodes Associated with Bipolar I Disorder | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: LT (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-000462-62 | Sponsor Protocol Number: Statex1 | Start Date*: 2015-09-23 |
Sponsor Name:Radboud university medical centre | ||
Full Title: The effects of statins on skeletal muscle mitochondria: is exercise the medicine? | ||
Medical condition: Asymp and symp statin users will undergo baseline measurements of skeletal muscle mitochondrial function and muscle function after which they will be switched to a single-blind placebo intervention... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
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