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Naltrexone for Early Problem Drinkers - Article


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Clinical Trial: Naltrexone for Early Problem Drinkers

This study has been completed.

Sponsored by: National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Information provided by: National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Purpose

Early problem drinkers are prevalent in the United States. Recent controlled trials have shown that brief interventions in the primary care setting can reduce drinking and alcohol-related problems in patients who lack evidence of alcohol dependence. Although naltrexone (Revia) has been approved for the treatment of alcohol dependence, few pharmacotherapy studies have been undertaken with early problem drinkers. This study is an 8-week trial of naltrexone versus placebo, combined with coping skills treatment that either focuses on targeted use of medication or serves as background to daily use of the medication. A total of 160 early problem drinkers recruited through screening in primary care medical settings will be randomly assigned to one of four treatment groups. Followup evaluations will be conducted at the end of treatment and again 3, 6, and 12 months.

Condition Treatment or Intervention Phase
Alcoholism
 Drug: naltrexone
Phase IV

MedlinePlus related topics:  Alcoholism

Study Type: Interventional
Study Design: Treatment, Randomized, Placebo Control, Efficacy Study

Official Title: Targeted Naltrexone for Early Problem Drinkers

Further Study Details: 

Expected Total Enrollment:  160

Study completion: September 2002

Eligibility

Ages Eligible for Study:  18 Years   -   60 Years,  Genders Eligible for Study:  Both

Criteria

Inclusion Criteria:

  • Limited to early problem drinkers (i.e., those with no more than mild alcohol dependence).
  • Have an average weekly alcohol consumption of greater than or equal to 24 standard drinks for men and 18 standard drinks for women.
  • Able to read English at the eighth grade or higher level and show no evidence of significant cognitive impairment.
  • Willing to provide a collateral informant for interviews regarding the patient's drinking during the study.
  • A woman of child-bearing potential must be non-lactating, practicing a reliable method of birth control, and have a negative pregnancy test prior to initiation of treatment.
  • Willing to provide a signed informed consent to participate in the study.

Exclusion Criteria:

  • Have a current clinically significant physical disease or abnormality.
  • Have a serious psychiatric illness.
  • Have a current diagnosis of drug dependence (other than nicotine dependence) or a lifetime diagnosis of opioid dependence.
  • A current diagnosis of alcohol dependence that is moderate or greater in severity or a history of alcohol withdrawal, or recurrent use of alcohol to alleviate alcohol withdrawal symptoms.
  • Used opioids or other psychoactive medications regularly in the month prior to study enrollment.
  • History of hypersensitivity to naltrexone (Revia).

Location Information


Connecticut
      Department of Psychiatry, University of Connecticut Health Center, Farmington,  Connecticut,  06030,  United States

More Information

Study ID Numbers:  NIAAAKRA11062
Record last reviewed:  November 2004
Last Updated:  November 22, 2004
Record first received:  November 2, 1999
ClinicalTrials.gov Identifier:  NCT00000455
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005


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