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Exploring the Efficacy and Biobehavioural Basis of Baclofen in the Treatment of Alcoholic Liver Disease
To explore the effectiveness and biobehavioural basis of baclofen in improving treatment outcomes for alcohol dependence in people with or without alcoholic cirrhosis in a double-blind randomised placebo-controlled trial.
This is a double-blind randomised placebo-controlled study investigating the efficacy of baclofen for the treatment of alcohol dependence in patients with alcoholic liver disease. Medications will be given for 12 weeks, with a further 6 months follow-up. Both male and female participants will be recruited to this study. Trial patients will be randomised to one of three treatment groups: (1) baclofen 30mg/day (10 mg t.i.d), (2) baclofen 75mg/day (25 mg t.i.d) or (3) Placebo (3 matched tabs/day). This study will also include a second, parallel group of patients with alcohol dependence (non alcoholic-liver disease patients) that will undergo the trial protocol as described above. These patients will be randomised according to a separate list into one of three treatment groups: (1) baclofen 30mg/day (10 mg t.i.d), (2) baclofen 75mg/day (25 mg t.i.d) or (3) Placebo (3 matched tabs/day).
Age
18 - 75 years
Sex
ALL
Healthy Volunteers
No
Drug Health Services, Royal Prince Alfred Hospital
Sydney, New South Wales, Australia
Start Date
March 1, 2013
Primary Completion Date
June 1, 2017
Completion Date
June 1, 2017
Last Updated
August 8, 2017
104
ACTUAL participants
Baclofen 30mg/day
DRUG
Baclofen 75mg/day
DRUG
Placebo
DRUG
Lead Sponsor
South West Sydney Local Health District
Collaborators
NCT06939088
NCT06265506
Data Source & Attribution
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