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Observational Study on Patients With Baclofen Treatment for Alcohol-dependence in France

Observational Study on Patients With Baclofen Treatment for Alcohol-dependence in French Gastro and Hepatology Departments

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02835365
Acronym
OBADE
Enrollment
218
Registered
2016-07-18
Start date
2015-01-01
Completion date
2018-09-30
Last updated
2023-01-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alcohol Drinking, Alcohol Withdrawal, Cirrhosis

Keywords

baclofen, alcohol, withdrawal

Brief summary

Baclofen is an agonist of the amino-butyricum B (GABA-B) receptor used for a long time in neurology to treat spastic contracture. Several clinical studies have suggested its efficacy in the treatment of alcohol-dependence in low, even in case of cirrhosis and high dose. French drug authority has authorized its use in 2012 whereas the l'European Association for the Study of the Liver recommends to perform additional studies on this indication. The goal of this observational study is to evaluate the use of baclofen for alcohol-dependence in real life care as well its efficacy.

Detailed description

Numerous centers of the French research group of the national association of the hepatologists and gastroenterologists from general hospitals (ANGH) will be part of this study. Patients treated with baclofen for alcohol -dependence will be enroll prospectively from 2014 and retrospectively if they were treated between 2012 and 2014. The reported alcohol consumption, biological markers of excessive alcohol, initial and usual baclofen dosage, blood balofen dosage as well as clinical data will be collected.

Interventions

None listed

Sponsors

Centre Hospitalier Intercommunal Creteil
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patients older than 18 years old * patient treated with baclofen therapy after 2012 for alcoholo-dependance

Exclusion criteria

* Baclofen therapy before 2012 * patient who refuse to participate

Design outcomes

Primary

MeasureTime frameDescription
Target populationat inclusionDemographic and clinical characteristics of patients who take baclofen for alcohol addiction: mean age, alcohol consumption, child pugh score, etc.

Secondary

MeasureTime frameDescription
baclofen posologyat inclusion, at 3, 6 and 12 months of follow-upused baclofen posology will be recorded to determine the posology scheme to treat patients with or without cirrhosis
Alcohol consumptionat inclusion, at 3, 6 and 12 months of follow-upEvolution of the alcohol consumption in patients under baclofen therapy
Biological markers of alcohol consumptionat inclusion, at 3, 6 and 12 months of follow-upEvolution of the biological markers of alcohol consumption in patients under baclofen therapy
baclofen toleranceat 3, 6 and 12 months of follow-upDescription of the side effects under baclofen therapy
Baclofen dosageat 3, 6 and 12 months of follow-upBlood baclofen dosage under baclofen treatment, if available

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026