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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 17 October 2012
Main ID:  NCT00372749
Date of registration: 05/09/2006
Primary sponsor: Assistance Publique - Hôpitaux de Paris
Public title: Does the Threat of an Aversive Reaction Affect Craving of Alcohol During Cue Exposure in Alcohol Dependent Patients?
Scientific title: Does the Threat of an Aversive Reaction Affect Craving of Alcohol During Cue Exposure in Alcohol Dependent Patients?
Date of first enrolment: October 2006
Target sample size: 30
Recruitment status: Completed
URL:  http://clinicaltrials.gov/show/NCT00372749
Study type:  Interventional
Study design:  Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment  
Countries of recruitment
France
Contacts
Name:   Henri Jean AUBIN, MD,
Address: 
Telephone:
Email:
Affiliation:  Assistance Publique - Hôpitaux de Paris
Key inclusion & exclusion criteria

Inclusion Criteria:

- Inpatients

- Alcohol dependence

- Detoxified since at least one week

- Willing to abstain from alcohol for at least 6 months

- Never treated with disulfiram

Exclusion Criteria:

- Any contra-indication to disulfiram

- Treated with and antidepressant or a neuroleptic medication within the 30 previous
days

- Treated with acamprosate, naltrexone, betablockers or clonidine within the 7
previous days

- Treated with benzodiazepines within the 3 previous days (except diazepam, maximum 30
mg/d)

- Anosmia



Age minimum: 18 Years
Age maximum: N/A
Gender: Both
Health Condition(s) or Problem(s) studied
Alcoholic Intoxication, Chronic
Intervention(s)
Behavioral: Aversive reaction during alcohol cue exposure
Primary Outcome(s)
Alcohol craving visual analogic evaluation [Time Frame: during de study]
Secondary Outcome(s)
Blood Pressure and Pulse Rate [Time Frame: during the study]
Secondary ID(s)
P051058
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Institut de Recherches Scientifiques sur les Boissons
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