- Trials with a EudraCT protocol (85)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (21)
85 result(s) found for: Intoxication.
Displaying page 1 of 5.
EudraCT Number: 2010-021446-21 | Sponsor Protocol Number: 00001 | Start Date*: 2010-12-28 | |||||||||||
Sponsor Name:Per Rosenberg | |||||||||||||
Full Title: Laskimonsisäisesti annetun rasvaemulsion kyky sitoa bupivakaiinia verenkierrossa | |||||||||||||
Medical condition: The study is performed on healthy volunteers, investigating lipid resuscitation from local anesthetic intoxication. | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002977-12 | Sponsor Protocol Number: EPUP81 | Start Date*: 2014-10-08 |
Sponsor Name:Maastriccht University | ||
Full Title: BRAIN KINETICS OF NEUROTRANSMISSION DURING THC INTOXICATION | ||
Medical condition: Brain functioning during THC intoxication | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002859-42 | Sponsor Protocol Number: OPNT002-AUD-001 | Start Date*: 2020-01-28 | |||||||||||
Sponsor Name:Opiant Pharmaceuticals Inc | |||||||||||||
Full Title: Randomised, double-blind, placebo-controlled trial evaluating the effects of naltrexone hydrochloride nasal spray on alcohol consumption in Alcohol Use Disorder | |||||||||||||
Medical condition: Alcohol use Disorder | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004921-27 | Sponsor Protocol Number: 1 | Start Date*: 2006-12-15 | |||||||||||
Sponsor Name:Psykiatrisk Center Gentofte | |||||||||||||
Full Title: Antabuse in severe alcoholism: an open controlled study | |||||||||||||
Medical condition: Alcoholism | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006886-18 | Sponsor Protocol Number: ALK21-014 | Start Date*: 2007-06-04 | |||||||||||
Sponsor Name:Alkermes Inc | |||||||||||||
Full Title: Efficacy and Safety of Vivitrol® in Adults Completing Inpatient Treatment for Alcohol Dependence | |||||||||||||
Medical condition: Alcohol Dependence | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019345-26 | Sponsor Protocol Number: 03-AnIt-10 | Start Date*: 2010-06-02 | |||||||||||
Sponsor Name:Department of Anesthesiology and Intensive Care, University Hospital Muenster | |||||||||||||
Full Title: Immunmodulatory effects of local anesthetics on neutrophils during sepsis | |||||||||||||
Medical condition: Sepsis and severe sepsis | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005902-30 | Sponsor Protocol Number: FAR01-2011 | Start Date*: 2012-02-13 | ||||||||||||||||
Sponsor Name:Servicio de Farmacia. Hospital Universitari de Bellvitge | ||||||||||||||||||
Full Title: | ||||||||||||||||||
Medical condition: | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001100-38 | Sponsor Protocol Number: FARM97AJNN | Start Date*: 2014-07-09 | |||||||||||
Sponsor Name:DIPART. DI NEUROSCIENZE, SCIENZE RIPRODUTTIVE E ODONTOSTOMATOLOGICHE DELL’UNIVERSITà DEGLI STUDI DI NAPOLI “FEDERICO II" | |||||||||||||
Full Title: Antagonists of Angiotensin II Receptors in sepsis | |||||||||||||
Medical condition: SEPSIS | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006984-21 | Sponsor Protocol Number: MAXSEP | Start Date*: 2007-05-29 | |||||||||||
Sponsor Name:Friedrich-Schiller-University of Jena | |||||||||||||
Full Title: prospective, randomized, open, multicentre trial to assess the influence of empiric antibiotic monotherapy with meropenem (Meronem) versus combination with moxifloxacin (Avalox) on the organ functi... | |||||||||||||
Medical condition: severe sepsis / septic shock | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004686-26 | Sponsor Protocol Number: 0594-020 | Start Date*: 2009-07-29 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: Ensayo clínico multicéntrico, aleatorizado, doble ciego, en fase II y en dos etapas para evaluar la eficacia y la seguridad de MK-0594 en pacientes con alcoholismo. A Phase II Multicenter, Randomi... | |||||||||||||
Medical condition: Dependencia Alcohólica Alcohol Dependence | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) BE (Completed) DE (Prematurely Ended) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002334-11 | Sponsor Protocol Number: 12014A | Start Date*: 2009-03-13 | |||||||||||
Sponsor Name:H. Lundbeck A/S | |||||||||||||
Full Title: Nalmefene Efficacy Study I: Randomised, double-blind, placebo-controlled, parallel-group, efficacy study of 20 mg nalmefene, as needed use, in patients with alcohol dependence | |||||||||||||
Medical condition: Alcohol dependence | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) SE (Completed) FI (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
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... | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000713-37 | Sponsor Protocol Number: 127 | Start Date*: 2006-02-20 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: Intervention Baclofen Intervention Study | |||||||||||||
Medical condition: treatment of dependence in alcohol addiction | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015537-67 | Sponsor Protocol Number: 2009-08-17 | Start Date*: 2009-11-23 | |||||||||||
Sponsor Name:Universitätsmedizin der Johannes Gutenberg-Universität Mainz | |||||||||||||
Full Title: Untersuchung der Wirksamkeit und Sicherheit von Vareniclin in der Postakutbehandlung der Alkoholabhängigkeit - eine prospektive, bizentrische, doppelblinde, placebokontrollierte, randomisierte Phas... | |||||||||||||
Medical condition: Alcohol dependence | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015837-55 | Sponsor Protocol Number: RAA09-004 | Start Date*: 2010-08-17 | |||||||||||
Sponsor Name:Kings College London [...] | |||||||||||||
Full Title: Double-blind, 36 month, placebo-controlled trial of mifepristone on cognition in alcoholics | |||||||||||||
Medical condition: Alcoholism | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002315-92 | Sponsor Protocol Number: 12013A | Start Date*: 2008-11-12 | |||||||||||
Sponsor Name:H. Lundbeck A/S | |||||||||||||
Full Title: A 52-week, randomised, double-blind, placebo-controlled, parallel-group, safety, tolerability and efficacy study of nalmefene, as needed use, in patients with alcohol dependence | |||||||||||||
Medical condition: Alcohol dependence | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) SK (Completed) EE (Completed) GB (Completed) LV (Completed) HU (Completed) LT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002563-27 | Sponsor Protocol Number: 12023A | Start Date*: 2008-11-24 | |||||||||||
Sponsor Name:H. Lundbeck A/S | |||||||||||||
Full Title: Nalmefene Efficacy Study II: Randomised, double-blind, placebo-controlled, parallel-group, efficacy study of 20 mg nalmefene, as needed use, in patients with alcohol dependence | |||||||||||||
Medical condition: Alcohol dependence | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) PT (Completed) ES (Completed) IT (Completed) BE (Completed) PL (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005318-35 | Sponsor Protocol Number: 172009 | Start Date*: 2009-01-29 | |||||||||||
Sponsor Name:Schering-Plough Research Institute | |||||||||||||
Full Title: A prospective, double-blind, placebo-controlled trial investigating the efficacy and safety of Org 25935 in relapse prevention in subjects with alcohol dependence. | |||||||||||||
Medical condition: Alcoholism | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) SE (Prematurely Ended) DE (Prematurely Ended) NL (Prematurely Ended) BE (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015168-32 | Sponsor Protocol Number: D0620C00003 | Start Date*: 2010-10-04 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A Multicentre, Randomised, Double Blind, Placebo controlled Phase IIb Study to compare the Efficacy and Safety of Two Dosing Regimens of Intravenous Infusions of CytoFab™ (AZD9773) in Adult Patient... | |||||||||||||
Medical condition: Severe sepsis and/or septic shock | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) FR (Completed) ES (Completed) CZ (Completed) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000069-57 | Sponsor Protocol Number: P15-01 | Start Date*: 2017-07-21 | |||||||||||
Sponsor Name:BIOPROJET PHARMA | |||||||||||||
Full Title: A Multisite Randomized Clinical Trial Evaluating BP1.3656 Versus Placebo For Alcohol Use Disorder Treatment | |||||||||||||
Medical condition: Male or female with moderate or severe DSM-5 alcohol use disorder (based on the alcohol use disorders section of MINI) | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
