This site became the new on June 19th. Learn more.
Show more Menu IMPORTANT: Listing of a study on this site does not reflect endorsement by the National Institutes of Health. Talk with a trusted healthcare professional before volunteering for a study. Read more... Menu IMPORTANT: Talk with a trusted healthcare professional before volunteering for a study. Read more... Menu
Give us feedback

Antabuse in Severe Alcoholism: an Open Controlled Study

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified March 2007 by Psykiatrisk Center Gentofte.
Recruitment status was:  Recruiting
Information provided by:
Psykiatrisk Center Gentofte Identifier:
First received: February 1, 2007
Last updated: March 2, 2007
Last verified: March 2007
Newly detoxified alcoholics (N=60) are randomised to either antabuse (disulfiram) treatment or the control group for a total of 6 months.All patients will receive cognitive behavioural treatment in groups. The hypothesis to be tested is that more of the patients who receive antabuse (disulfiram) will be alcohol free during the 6 months treatment period compared to the control group. The trial is open.

Condition Intervention Phase
Alcoholism Drug: antabuse (disulfiram) Phase 4

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Antabuse in Severe Alcoholism: an Open Controlled Study

Resource links provided by NLM:

Further study details as provided by Psykiatrisk Center Gentofte:

Primary Outcome Measures:
  • The number of patients in each group who have not been drinking alcohol after 6 months of treatment.

Estimated Enrollment: 60
Study Start Date: February 2007
Estimated Study Completion Date: June 2009

Ages Eligible for Study:   18 Years to 70 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Alcoholism
  • Living in the departments catchment area

Exclusion Criteria:

  • Pregnancy
  • Schizophrenia
  • Bipolar disorder
  • Other substance abuse
  • Dementia
  • Anorexia
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT00431262

Psykiatrisk Center Gentofte Recruiting
Hellerup, Denmark, 2900
Contact: Jakob Ulrichsen, MD, ph.d.    (45) 3977 3650   
Principal Investigator: Jakob Ulrichsen, MD, ph.d.         
Sponsors and Collaborators
Psykiatrisk Center Gentofte
Principal Investigator: Jakob Ulrichsen, MD, ph.d. Psykiatrisk Center Gentofte
  More Information Identifier: NCT00431262     History of Changes
Other Study ID Numbers: EudraCT no. 2006-004921-27
Study First Received: February 1, 2007
Last Updated: March 2, 2007

Keywords provided by Psykiatrisk Center Gentofte:
cognitive behavioural therapy

Additional relevant MeSH terms:
Alcohol-Related Disorders
Substance-Related Disorders
Chemically-Induced Disorders
Mental Disorders
Alcohol Deterrents
Acetaldehyde Dehydrogenase Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action processed this record on August 21, 2017