Antabuse in Severe Alcoholism: an Open Controlled Study

NCT ID: NCT00431262

Last Updated: 2007-03-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

PHASE4

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2007-02-28

Study Completion Date

2009-06-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Alcoholism

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

antabuse (disulfiram)

Intervention Type DRUG

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Alcoholism
* Living in the departments catchment area

Exclusion Criteria

* Pregnancy
* Schizophrenia
* Bipolar disorder
* Other substance abuse
* Dementia
* Anorexia
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Psykiatrisk Center Gentofte

OTHER

Sponsor Role lead

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Jakob Ulrichsen, MD, ph.d.

Role: PRINCIPAL_INVESTIGATOR

Psykiatrisk Center Gentofte

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Psykiatrisk Center Gentofte

Hellerup, , Denmark

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Denmark

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Jakob Ulrichsen, MD, ph.d.

Role: primary

(45) 3977 3650

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

EudraCT no. 2006-004921-27

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

PT150 Drug for Use in Alcohol Use Disorder
NCT06712602 RECRUITING PHASE1
ABT-436 for Alcohol Dependence
NCT01613014 COMPLETED PHASE2
Study of DCR-AUD in Healthy Volunteers
NCT05021640 COMPLETED PHASE1
Varenicline for Alcohol Dependence
NCT01146613 COMPLETED PHASE2