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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00435435
Other study ID # KTL-175-1
Secondary ID
Status Completed
Phase Phase 4
First received February 14, 2007
Last updated February 15, 2007
Start date September 2000
Est. completion date April 2005

Study information

Verified date February 2000
Source National Institute for Health and Welfare, Finland
Contact n/a
Is FDA regulated No
Health authority Finland: Finnish Medicines Agency
Study type Interventional

Clinical Trial Summary

The aim of this study was to compare the effect of manual based cognitive therapy in adjunct of three different pharmacotherapy.


Description:

Context Alcoholism is common clinical problem and its treatment has no standard and is controversy. Different pharmacotherapy’s, acamporsate, nalterxone and disulfiram have shown to improve the drinking outcomes, but there is no randomized comparative studies on the effects of these three medications.

Objectives The aim of this study was to compare the effect of manual based cognitive therapy in adjunct of three different pharmacotherapy.

Design and setting Randomized, open label, multicentre naturalistic study, 12 week continuous medication followed by targeted medication up to 52weeks and 67 week follow up on voluntary treatment seeking alcohol dependent outpatients.

Participants 243 alcohol dependent adults. Intervention Subjects were randomized 1:1:1 to receive naltrexone, acamprosate or disulfiram, 50 mg, 1998 mg or 200 mg correspondingly per day. The patients were met weekly in first month, then after 3, 6 and 12 months.


Recruitment information / eligibility

Status Completed
Enrollment 243
Est. completion date April 2005
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 25 Years to 65 Years
Eligibility Inclusion Criteria:

- Alcohol dependence (ICD-10)

Exclusion Criteria:

- Clinically significant symptoms of alcohol withdrawal

- Significant recently diagnosed psychiatric disease (psychosis, personality disorder or suicidal tendency that appeared during the initial interview)

- Current psychiatric disease demanding special treatment or medication including DSM-IV determined drug dependence other than alcohol or nicotine dependence

- Current use of any opioids within four weeks before screening

- Significant brain, thyroid, kidney, uncompensated heart disease, or clinically significant liver disease (cirrhosis, aqlcoholic hepatitis or ALAT > 200)

- Pregnancy, nursing, or women refused to use a reliable method for birth control

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Disulfiram

Acamprosate

Naltexone


Locations

Country Name City State
Finland National Public Health Institute, Department of Mental Health and Alcohol Research Helsinki

Sponsors (1)

Lead Sponsor Collaborator
National Institute for Health and Welfare, Finland

Country where clinical trial is conducted

Finland, 

References & Publications (1)

Morley KC, Teesson M, Reid SC, Sannibale C, Thomson C, Phung N, Weltman M, Bell JR, Richardson K, Haber PS. Naltrexone versus acamprosate in the treatment of alcohol dependence: A multi-centre, randomized, double-blind, placebo-controlled trial. Addiction. 2006 Oct;101(10):1451-62. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Time(days) to first heavy drinking (HDD)day after medication started
Secondary Time (days) to first drinking after medication started
Secondary Abstinence days (0 drinks/ day) by group
Secondary Average alcohol intake (weekly by group)
Secondary ALAT
Secondary GGT
Secondary SADD
Secondary AUDIT
Secondary EQ-5
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