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Main
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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. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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17 October 2012 |
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Main ID: |
NCT00372749 |
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Date of registration:
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05/09/2006 |
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Primary sponsor: |
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Public title:
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Does the Threat of an Aversive Reaction Affect Craving of Alcohol During Cue Exposure in Alcohol Dependent Patients?
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Scientific title:
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Does the Threat of an Aversive Reaction Affect Craving of Alcohol During Cue Exposure in Alcohol Dependent Patients? |
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Date of first enrolment:
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October 2006 |
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Target sample size:
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30 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT00372749 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment
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Countries of recruitment
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France
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Contacts
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Name:
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Henri Jean AUBIN, MD, |
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Address:
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Telephone:
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Email:
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Affiliation:
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Assistance Publique - Hôpitaux de Paris |
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Key inclusion & exclusion criteria
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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
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Health Condition(s) or Problem(s) studied
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Alcoholic Intoxication, Chronic
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Intervention(s)
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Behavioral: Aversive reaction during alcohol cue exposure
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Primary Outcome(s)
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Alcohol craving visual analogic evaluation
[Time Frame: during de study]
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Secondary Outcome(s)
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Blood Pressure and Pulse Rate
[Time Frame: during the study]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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