Safety & Efficacy of Baclofen for Alcohol Withdrawal in Chronic Liver Disease With Active Alcohol Consumption
Condition(s) studied
Investigational drug(s) / intervention(s)
Baclofen: Safety and effectiveness of baclofen as a treatment for alcohol withdrawal in patients with chronic liver disease. The investigators will administer baclofen in increasing doses up to a maximum dose of 10 mg every 8 hours, evaluating the drug's tolerance and its effectiveness in achieving alcohol abstinence. Baclofen will be administered during the patient's hospitalization for decompensation of their liver disease, in patients followed up as outpatients in hepatology clinics, and in those managed as outpatients by psychiatrists specializing in addiction
Study summary
This study examines the safety and effectiveness of baclofen as a treatment for alcohol withdrawal in patients with chronic liver disease who continue drinking. It aims to evaluate baclofen's ability to promote alcohol abstinence or reduction while monitoring adverse effects. Secondary outcomes include liver function changes, hospital readmissions, and complications of cirrhosis.
Alcohol consumption worsens liver disease prognosis, yet alcohol use disorder (AUD) often goes untreated. Baclofen, which is safe for patients with liver impairment, is recommended as a first-line treatment for AUD in chronic liver disease. This prospective study collects data from patients treated with baclofen at Parc Taulí Hospital, analyzing outcomes at three and six months to assess abstinence, alcohol reduction, and adverse effects.
Eligibility
Primary outcome measure(s)
- Rate of patients who achieve abstinence — During 6 months
The investigators will report, through clinical interviews, the percentage of patients who have stopped drinking - Rate of patients who reduce alcohol consumption — During 6 months
The investigators will report, through clinical interviews, the percentage of patients who have reduced alcohol consumption
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Consorci Corporació Sanitària Parc Taulí | Sabadell | Barcelona |
More Corporacion Parc Tauli trials in Spain
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06840652 on ClinicalTrials.gov ↗ ← All trials in Spain