- Trials with a EudraCT protocol (72)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
72 result(s) found for: Drug Abuse AND Alcohol Abuse.
Displaying page 1 of 4.
EudraCT Number: 2016-000207-90 | Sponsor Protocol Number: P15-14/BF2.649 | Start Date*: 2016-11-24 | |||||||||||
Sponsor Name:BIPROJET PHARMA | |||||||||||||
Full Title: A Multisite Randomized, Double-Blind, Placebo-Controlled Trial Evaluating Pitolisant (BF2.649) For Alcohol Use Disorder Treatment. | |||||||||||||
Medical condition: Patients with moderate to severe alcohol use disorder | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Prematurely Ended) | |||||||||||||
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: 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: 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 |
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 | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002547-42 | Sponsor Protocol Number: BIMA2016 | Start Date*: 2017-02-20 | |||||||||||
Sponsor Name:Imperial College London, Joint Research Compliance Office | |||||||||||||
Full Title: Open-Label Proof of Concept Feasibility Study to Explore the Safety, Tolerability and Potential Role of MDMA-Assisted Psychotherapy for the Treatment of Detoxified Patients with Alcohol Use Disorder. | |||||||||||||
Medical condition: Alcohol Use Disorder | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001929-20 | Sponsor Protocol Number: TEST-APO | Start Date*: 2010-05-18 | |||||||||||||||||||||
Sponsor Name:Servicio de Psiquiatría. Hospital Universitari Vall dHebron | |||||||||||||||||||||||
Full Title: EL TEST DE APOMORFINA COMO MARCADOR BIOLÓGICO DE LAS RECAÍDAS EN PACIENTES DEPENDIENTES DE SUSTANCIAS PSICOTROPAS | |||||||||||||||||||||||
Medical condition: Dependencia de alcohol Dependencia de cocaína Dependencia de heroína | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||||||||||||
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: 2019-001834-33 | Sponsor Protocol Number: OXYLIFE | Start Date*: 2020-10-20 |
Sponsor Name:LABORATORIO FARMACEUTICO CT SRL | ||
Full Title: Efficacy and safety of Sodium Oxybate in reducing alcohol consumption and maintaining abstinence in alcohol-dependent subjects with high and very high drinking risk level. “OXYLIFE Study“ | ||
Medical condition: Alcohol addiction | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: IT (Trial now transitioned) | ||
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 | |||||||||||||
|
|||||||||||||
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: 2018-001386-16 | Sponsor Protocol Number: TUD-TEMACA-069 | Start Date*: 2019-07-16 |
Sponsor Name:Technische Universität Dresden | ||
Full Title: Investigation of the efficacy of acamprosate and calcium in comparison to placebo as validation of a behavioural test for alcohol dependence (TEMACA) | ||
Medical condition: persons with disturbance in alcohol use according DSM5 which do not want to change their alcohol consumption | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-005235-14 | Sponsor Protocol Number: P05042 | Start Date*: 2007-07-11 | |||||||||||
Sponsor Name:Integrated Therapeutics Group Inc | |||||||||||||
Full Title: A Randomized Acceptability and Safety Study of Suboxone Induction in Heroin Users | |||||||||||||
Medical condition: Opioid dependence | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) GB (Completed) ES (Completed) CZ (Completed) PT (Completed) SI (Completed) DE (Completed) IE (Completed) IT (Completed) LT (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-002462-32 | Sponsor Protocol Number: SHW01 | Start Date*: 2022-12-09 | |||||||||||
Sponsor Name:Suchthilfe Wien gGmbH | |||||||||||||
Full Title: Pilot study on the safety and feasibility of intravenous opioid agonist therapy (OAT) with Hydagelan® (hydromorphone hydrochloride) in Vienna. | |||||||||||||
Medical condition: Opioid dependence: Opioid dependence is a serious and usually chronic disease that requires treatment, encompasses various psychological and physical dimensions, and is associated with concomitant ... | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013647-10 | Sponsor Protocol Number: 2P50-DA012756-11 | Start Date*: 2009-12-10 |
Sponsor Name:National Institute on Drug Abuse (NIDA) | ||
Full Title: Extended Release Naltrexone for Treating Amphetamine Dependence in Iceland | ||
Medical condition: Amphetamine dependence | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IS (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-005234-21 | Sponsor Protocol Number: P04843 | Start Date*: 2007-11-28 | |||||||||||
Sponsor Name:Schering-Plough Research Institute | |||||||||||||
Full Title: A Randomized Acceptability and Safety Study of the Transfer From Subutex to Suboxone in Opioid-Dependent Subjects. | |||||||||||||
Medical condition: Opioid dependance | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) GB (Completed) SE (Completed) PT (Completed) DK (Completed) LT (Completed) SI (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002708-26 | Sponsor Protocol Number: CRC341 | Start Date*: 2017-06-28 | ||||||||||||||||
Sponsor Name:University of Surrey | ||||||||||||||||||
Full Title: A randomised double blind placebo controlled pilot trial of oxytocin efficacy in treating detoxified opioid dependent individuals | ||||||||||||||||||
Medical condition: Opioid dependence. The study will be investigating the efficacy of Syntocinon (oxytocin) on treating the withdrawal symptoms and cravings that opioid (e.g. almost always heroin) dependent individua... | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-001088-28 | Sponsor Protocol Number: BRIO | Start Date*: 2016-01-14 | ||||||||||||||||
Sponsor Name:South London and Maudsley NHS Foundation Trust [...] | ||||||||||||||||||
Full Title: Feasibility, efficacy and acceptability of injected buprenorphine as treatment for opiate users who persist in injecting illicit heroin through opiate maintenance treatment | ||||||||||||||||||
Medical condition: Addiction to illicit heroin | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-002147-27 | Sponsor Protocol Number: | Start Date*: 2005-05-26 |
Sponsor Name:Department of General Psychiatry | ||
Full Title: Influence of treatment of olanzapine and ziprasidone on transcapillary glucose transport in human skeletal muscle | ||
Medical condition: Healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-004710-95 | Sponsor Protocol Number: REPAS161118 | Start Date*: 2018-02-07 |
Sponsor Name:Beroendecentrum Stockholm | ||
Full Title: Extended-release injectable suspension naltrexone (XR-NTX) as an adjunt pharmacotherapy for prevention of substance use in patients with SUD who are currently in treatment for ADHD: A multicenter r... | ||
Medical condition: Amphetamine dependence and ADHD (Attention-Deficit/Hyperactivity Disorder) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2010-020953-14 | Sponsor Protocol Number: PosaBupreversion1.0 | Start Date*: 2010-08-12 |
Sponsor Name:Derartment of Anaesthesiology and Intensive Care, Turku University Hospital | ||
Full Title: Effects of posaconazole and voriconazole on the pharmacokinetics and pharmacodynamics of sublingual buprenorphine: A three-phase double-blind cross-over study in healthy subjects. | ||
Medical condition: - healty volunteer subjects - The study is aimed to examine the possible interactions of low-dose sublingual buprenorphine with posaconazole and voriconazole. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
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. |
