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1 for Alcoholism (SAFADIE Trial)

Phase 4
Waitlist Available
Led By Florian Birkmayer, M.D.
Research Sponsored by University of New Mexico
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up patients will receive acamprosate for 12 weeks.the schedule of visits will include screening, baseline and and three monthly follow-up visits at days 30, 60 and 90. we will recruit 25 subjects in the total study period of 12 month.
Awards & highlights

SAFADIE Trial Summary

Alcohol abuse and dependence are very prevalent and result in significant morbidity, mortality and cost to society (Harwood 2000). Pharmacotherapies to assist with alcohol dependence consist of disulfiram, naltrexone and acamprosate. Of these, acamprosate is unique in that it is not metabolized by the liver, but rather completely excreted renally. In contrast, naltrexone is metabolized by the CYP450 system of the liver and less than 2% is excreted unchanged and can cause liver damage (PDR 2005). Multiple cases of hepatitis, including both cholestatic and fulminant hepatitis, as well as hepatic failure resulting in transplantation or death, have been reported with administration of disulfiram (PDR 2005). The incidence of liver disease among alcoholics is high and increases with age and years of drinking and this may preclude the use of antabuse or naltrexone to help alcohol dependent patients with liver disease or that are elderly . Thus acamprosate has a unique safety profile that would make it ideally suited for treating alcohol dependence in the elderly, even in the presence of hepatic impairment. The current study is to evaluate the safety profile of acamprosate in elderly patients with alcohol dependence. Acamprosate, calcium acetyl homotaurinate, has been approved in most European countries and the U.S. for the maintenance of abstinence in recently detoxified alcoholics. The mechanism of action involves primarily the restoration of a normal N-methyl- D -aspartate (NMDA) receptor tone in glutamatergic systems (Rammes et al 2001). Several trials of acamprosate confirm its efficacy in the maintenance of abstinence in alcohol dependence (Lesch et al. 2001; Slattery et al. 2003; Mann et al. 2004; Verheul et al. 2004). It also reduces the severity of relapse in alcoholics in abstinence based treatment programs (Chick et al. 2003). There is limited data on the safety of acamprosate in the elderly (PDR 2005). For the purposes of this study, elderly will be defined as 60 years or older. STUDY OBJECTIVE: To determine the short-term safety of Acamprosate in the treatment of alcohol dependence in the elderly.

Eligible Conditions
  • Alcoholism

SAFADIE Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~patients will receive acamprosate for 12 weeks.the schedule of visits will include screening, baseline and and three monthly follow-up visits at days 30, 60 and 90. we will recruit 25 subjects in the total study period of 12 month.
This trial's timeline: 3 weeks for screening, Varies for treatment, and patients will receive acamprosate for 12 weeks.the schedule of visits will include screening, baseline and and three monthly follow-up visits at days 30, 60 and 90. we will recruit 25 subjects in the total study period of 12 month. for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
The will be safety.
Secondary outcome measures
Changes in the quantity of alcohol consumed as determined by Time Line Follow Back assessment by patient and parallel historian will be determined.

SAFADIE Trial Design

1Treatment groups
Experimental Treatment
Group I: 1Experimental Treatment2 Interventions
Acamprosate(Campral)
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Acamprosate
FDA approved
Acamprosate
FDA approved

Find a Location

Who is running the clinical trial?

University of New MexicoLead Sponsor
372 Previous Clinical Trials
3,528,789 Total Patients Enrolled
15 Trials studying Alcoholism
2,756 Patients Enrolled for Alcoholism
Florian Birkmayer, M.D.Principal InvestigatorUniversity of New Mexico, Department of Psychiatry

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~0 spots leftby Apr 2025