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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02349477
Other study ID # Pro00032587
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date November 2014
Est. completion date August 27, 2018

Study information

Verified date October 2019
Source Medical University of South Carolina
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This treatment study is a 16-weeks outpatient clinical trial where subjects with alcohol dependence will get medication, which might help them to reduce or stop their drinking, or a placebo ( placebo is a capsule that looks the same as the investigational drug, but has no real medication. It is a "sugar pill").


Description:

This treatment study is a 16-weeks outpatient clinical trial where subjects will get medication, which might help them to reduce or stop their drinking or a placebo ( placebo is a capsule that looks the same as the investigational drug, but has no real medication. It is a "sugar pill"). This study will recruit and randomize subjects who have expressed an interest in receiving treatment for alcohol dependence. Upon enrollment into this study there will be 11 outpatient visits. Each visit will last about 1-1.5 hours.


Recruitment information / eligibility

Status Completed
Enrollment 96
Est. completion date August 27, 2018
Est. primary completion date August 27, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

1. Meets criteria for alcohol use disorder based on DSM-5 criteria

2. Meets criteria for history of alcohol withdrawal based on DSM-5 criteria

3. Able to maintain abstinence for a minimum of 3 days prior to randomization as verified by self report, urine ETG, and breathalyzer.

Exclusion Criteria:

1. Significant psychiatric or medical illness

2. No other substance abuse

3. Taking other medications known to treat alcohol use disorder

4. Unstable living arrangements

5. Significant legal problems pending

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Gabapentin
gaba potentiating medication
Placebo
a pill that looks exactly like the active medication but does not contain medication

Locations

Country Name City State
United States Medical University of South Carolina Charleston South Carolina

Sponsors (1)

Lead Sponsor Collaborator
Medical University of South Carolina

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Number of Participants With No Drinking Days by AWS Score and Medication This analysis examines the interaction of medication group with a median split of the baseline Alcohol Withdrawal Scale (AWS) scores on the primary outcome variable (no heavy drinking days, corrected for %dCDT). Participants will report their daily alcohol use with using a daily calendar. AWS ranges from 0 to 44 where higher values correspond with more serious withdrawal (worse outcome). 4 months
Primary Percent of Subjects With no Heavy Drinking Days (PSNHDD) The primary dependent variable will be the percent of subjects with no heavy drinking days (4 or more standard drinks for women and 5 or more standard drinks for men). Participants will report their daily alcohol use with using a daily calendar. No heavy drinking days is corrected for %dCDT. 4 months
Secondary Percent of Subjects With no Drinking Days (PSNDD) The secondary dependent variable will be percent of subjects with no drinking days (total abstinence). Participants will report their daily alcohol use with using a daily calendar. Abstinence is corrected for %dCDT. 4 months
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