- Trials with a EudraCT protocol (101)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
101 result(s) found for: Drinking.
Displaying page 3 of 6.
EudraCT Number: 2006-003999-35 | Sponsor Protocol Number: Kep-F10.2.01 | Start Date*: 2007-01-11 |
Sponsor Name:Charité Campus Mitte, Klinik für Psychiatrie und Psychotherapie | ||
Full Title: Efficacy and safety of levetiracetam in prevention of alcohol relapse in recently detoxified alcohol dependent patients | ||
Medical condition: detoxified alcohol dependent outpatients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
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: 2004-004514-17 | Sponsor Protocol Number: 11111918 | Start Date*: 2005-03-29 |
Sponsor Name:Beroendcentrum Stockholm | ||
Full Title: Does Acamprosate Decrease Cue-induced Alcohol Craving? | ||
Medical condition: Alcohol dependence. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-005286-24 | Sponsor Protocol Number: 22112015 | Start Date*: 2016-02-24 |
Sponsor Name: | ||
Full Title: Baclofen in managing acute alcohol withdrawal | ||
Medical condition: Alcohol withdrawal syndrome | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-000575-14 | Sponsor Protocol Number: SMO032/10/03 | Start Date*: 2012-05-09 | |||||||||||
Sponsor Name:D&A PHARMA | |||||||||||||
Full Title: Randomized, multicenter, double-blind, placebo-controlled study of the safety and efficacy of 4 dose regimens of SMO.IR, an oral solid formulation of sodium oxybate, in the maintenance of alcohol a... | |||||||||||||
Medical condition: maintenance of alcohol abstinence in recently abstinent alcohol-dependent patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) CZ (Completed) AT (Completed) IT (Completed) SK (Completed) DE (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-007090-72 | Sponsor Protocol Number: lpdc07 | Start Date*: 2007-10-17 | |||||||||||
Sponsor Name:Central Institute of Mental Health | |||||||||||||
Full Title: The role of the glutamatergic system in the extinction of conditioned reinforcement processes | |||||||||||||
Medical condition: Alcohol-dependence is an important factor contributing to health care costs. Alcohol-dependent patients show conditioned reactions to stimuli that were associated with substance consumption and sev... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000737-39 | Sponsor Protocol Number: AD04-301 | Start Date*: 2020-04-28 | |||||||||||
Sponsor Name:Adial Pharmaceuticals Inc. | |||||||||||||
Full Title: A 24-Week, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Phase 3 Clinical Study to Evaluate the Efficacy, Safety and Tolerability of AD04 (Ondansetron) in Adults with A... | |||||||||||||
Medical condition: Adult patients diagnosed with moderate or severe alcohol use disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) FI (Completed) BG (Completed) PL (Completed) EE (Completed) LV (Completed) HR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001211-39 | Sponsor Protocol Number: ALK3831-401 | Start Date*: 2015-01-27 |
Sponsor Name:Alkermes, Inc. | ||
Full Title: A Phase 2, Efficacy, Safety, and Tolerability Study of ALKS 3831 in Schizophrenia with Alcohol Use Disorder | ||
Medical condition: Schizophrenia with alcohol use disorder | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BG (Completed) PL (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-000222-11 | Sponsor Protocol Number: 1 | Start Date*: 2016-02-04 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: A phase II, randomised, double-blind, placebo- controlled, multi-site, parallel group clinical trial to examine ketamine as a pharmacological treatment for alcohol dependence in an alcohol dependen... | |||||||||||||
Medical condition: Severe Alcohol Use Disorder | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003005-41 | Sponsor Protocol Number: CS0866-A-U101 | Start Date*: 2015-07-24 |
Sponsor Name:Sankyo Pharma Development | ||
Full Title: A Comparative, Randomized, Single-Dose, 2-Way Crossover Bioavailability Study of a Compounded 4 mg/mL Olmesartan Medoxomil Suspension (Total Dose 40 mg) and 40 mg Olmesartan Medoxomil Tablets (Beni... | ||
Medical condition: Not applicable - Healthy Volunteer study | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2015-001245-89 | Sponsor Protocol Number: BDR4580 | Start Date*: 2015-04-13 | |||||||||||
Sponsor Name:Sanofi-aventis | |||||||||||||
Full Title: Relative bioavailability study between 75 mg tablet and 75 mg solution of Clopidogrel (SR25990C) after single oral administration to young healthy men. Open, crossover, randomized and monocenter study | |||||||||||||
Medical condition: Young healthy men (intended indication cardiovascular disease) | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002913-11 | Sponsor Protocol Number: DOP 06 | Start Date*: 2006-07-31 |
Sponsor Name:York Hospitals NHS Trust | ||
Full Title: Randomised controlled, double blinded single centre trial to assess the effects of peri-operative dopexamine on morbidity after major abdominal surgery in patients with low anaerobic threshold. | ||
Medical condition: Patients undergoing scheduled resection for carcinoma of the colon, rectum, bladder, pancreas, stomach or kidney, who, after routine CPX testing at the Pre-assessment Clinic, have been found to hav... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-002836-26 | Sponsor Protocol Number: DDD13POSA | Start Date*: 2014-01-09 |
Sponsor Name:KU Leuven - Drug Delivery & Disposition | ||
Full Title: Gastrointestinal behavior of posaconazol in healthy human volunteers | ||
Medical condition: Suspension: 105 mg posaconazol (2.6 ml Noxafil): 1)with 250 ml water 2)with 250 ml sparkling water 3)with 5 lumps of sugar, dissolved in 250 ml water 3)with 5 lumps of sugar, dissolved in 250 ml of... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-003849-32 | Sponsor Protocol Number: AGI003-007 (ARDIS-3) | Start Date*: 2007-10-22 | |||||||||||
Sponsor Name:AGI Therapeutics Research Ltd | |||||||||||||
Full Title: An Open-label, Roll-over Safety Study of AGI-003 (Arverapamil) in the Treatment of Irritable Bowel Syndrome with Diarrhea (IBS-D) | |||||||||||||
Medical condition: Irritable Bowel Syndrome with Diarrhea (IBS-D) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) PL (Prematurely Ended) CZ (Prematurely Ended) LT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003129-92 | Sponsor Protocol Number: 11-1-039 | Start Date*: 2012-06-04 |
Sponsor Name:MUMC+ | ||
Full Title: The Orange III trial: Optimised recovery with Movicol preoperatively within an enhanced recovery programme, a randomised controlled trial | ||
Medical condition: Liver resection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-001948-60 | Sponsor Protocol Number: DOSFEM | Start Date*: 2013-09-09 |
Sponsor Name:Sint Franciscus Gasthuis Rotterdam | ||
Full Title: Effects of high and low dose vitamin D on postprandial leukocyte activation, oxidative stress and vascular function in healthy overweight and obese females | ||
Medical condition: 'healthy volunteers' 'atherosclerosis' 'vitamin D deficiency' | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-001611-20 | Sponsor Protocol Number: 357-0-0 | Start Date*: 2018-07-24 |
Sponsor Name:University of Tübingen | ||
Full Title: Pathophysiology-based therapy of epileptic encephalopathies | ||
Medical condition: patients with epileptic encephalopathies | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2010-021861-62 | Sponsor Protocol Number: BACLAD | Start Date*: 2010-12-10 |
Sponsor Name:Charité - Universitätsmedizin Berlin | ||
Full Title: Baclofen for the Treatment of Alcohol Dependence | ||
Medical condition: Alcohol Dependence | ||
Disease: | ||
Population Age: | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-005006-66 | Sponsor Protocol Number: 2013118 | Start Date*: 2014-01-21 |
Sponsor Name:Procter and Gamble | ||
Full Title: A 2-arm, randomised, single - (Investigator) blind, controlled, parallel design study in common cold sufferers experiencing nasal congestion to assess the speed of action of Vicks® VapoRub® (VVR) | ||
Medical condition: Nasal congestion due to common cold in adults | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-004298-20 | Sponsor Protocol Number: MAMCAC02102014 | Start Date*: 2015-02-03 |
Sponsor Name:Stockholm Centre for Dependency Disorders | ||
Full Title: The effect of methylphenidate on executive functioning in amphetamine dependent individuals with ADHD | ||
Medical condition: Amphetamine dependence | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
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