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Completed

NCT Number: NCT00846859

Does Varenicline Influence Alcohol Consumption in Alcohol Dependent Individuals?

The aim of the present clinical trial is to investigate whether 14 weeks of treatment with a prescription medication for smoking cessation (European trade name: Champix(R); US trade name: Chantix(R)), can reduce alcohol consumption in alcohol dependent individuals.

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Key information

Age range

30 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Addiction Biology Unit, Beroendekliniken, University of Gothenburg and Sahlgrenska University Hospital, Gothenburg, Sweden

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age: 30-70 years at screening
  • Alcohol dependence according to DSM-IV (meeting ≥3 out of 7 criteria)
  • ≥ 20 heavy drinking days (men: ≥ 5 drinks/day, women: ≥4 drinks/day, where 1 std. drink is defined as 12 g ethanol) during the last 60 days
  • Participants must have signed the informed consent

Exclusion criteria

  • Subject to treatment of alcohol withdrawal within 30 days of study initiation
  • Subject to treatment that may affect alcohol consumption including acamprosate, naltrexone, disulfiram, ondansetron, topiramate, SSRIs, varenicline, mirtazapine, rimonabant, methylphenidate or atomoxetine within 3 months of study initiation
  • Subject to treatment of depression within 3 months of study initiation
  • The continuous use of drugs such as codeine, hydroxyzine, alimemazine, benzodiazepines or sedatives (the sporadic use of these compounds is accepted)
  • Any concurrent medication that may affect the results of the trial or is considered to compromise the safety of the participants in the trial
  • History of Delirium Tremens the last 5 years or any history of abstinence-induced seizures
  • Laboratory hepatic values of more than 3 times the upper limit of the normal range or other clinically significant abnormalities in the screening laboratory values.
  • Participants who are pregnant or nursing infant(s), and women of childbearing potential not using a contraceptive method judged by the investigator to be effective.
  • Any ongoing serious psychiatric or somatic disorder
  • Any psychiatric Axel I diagnoses (except for nicotine or alcohol dependence)
  • The concurrent use of illicit drugs based on urine-toxicity test
  • The need for detoxification
  • Diabetes Mellitus Type 1
  • Suicidal risk
  • Homelessness
  • Additional factors that implies to the investigator/physician that the participant will not be completing the study

Treatment and study plan

varenicline (Champix/Chantix)

Drug

14 weeks of per oral tablet treatment in an escalating dosing regimen (0.5 mg - 1.0 mg/day; 1 - 2 tablets/day).

Other names: Champix(R)/Chantix(R)

Placebo for varenicline

Drug

14 weeks of per oral tablet treatment in an escalating dosing regimen (1 - 2 tablets/day)

Other names: placebo for Champix(R) / Chantix(R)

Primary outcomes

  1. Alcohol consumption as measured by diary and questionnaires: the number of heavy drinking days (as percentage) defined as ≥5 standard drinks per day for men and ≥4 standard drinks per day for women

Secondary outcomes

  1. Alcohol consumption as measured by diary and questionnaires: total amount (grams) of consumed alcohol compared to baseline.

  2. Percentage (and number) of abstaining days compared to baseline.

  3. Drinks per drinking day compared to baseline.

  4. Alcohol consumption as measured by alcohol markers in blood compared to baseline.

  5. Nicotine use in alcohol dependent subjects as measured by diary and questionnaires compared to baseline.

  6. Compliance as measured by diary and returned medication packages.

Sponsors and collaborators

Lead sponsor

Sahlgrenska University Hospital

Other

Collaborators

  • Karolinska University Hospital
  • Malmö University

Registry information

Important dates

Study start
2009
Primary completion
2010
Study completion
2011
First posted
Feb 19, 2009
Registry last updated
Jul 21, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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