University of Connecticut Health Center
Farmington, Connecticut, 06030, United States
NCT Number: NCT00368550
The purpose of this study is to determine whether Sertraline, compared to placebo, is effective in the treatment of alcohol dependence as a function of the subtype of alcoholic patient being treated. This involved administering sertraline (to a maximum of 200 mg/day) or an inactive placebo for a 14-week treatment period.
Looking for future studies?
Notify Me18 year–65 year
All sexes
Interventional
Phase 4
Farmington, Connecticut, 06030, United States
In an effort to broaden the options for pharmacotherapy of alcoholism, this study will examine the effects of sertraline, a selective serotonin reuptake inhibitor (SSRI), for the treatment of alcohol dependence. The study is based on evidence that, although SSRI therapy is not appropriate for all alcoholics, there exists a substantial subgroup of alcoholics for whom SSRIs appear to exert a clinically important effect. Sertraline is among the most widely prescribed psychotropic medications in the world. Consequently, this study will examine the safety and efficacy of sertraline, the mechanism and duration of those effects and the best method for subtyping alcoholics to identify individuals for whom the medication is most likely to produce a clinically important reduction in drinking behavior.
The study employs a parallel-group, prospective design in which randomization is balanced on patient subtype (early-onset/late-onset) and other relevant pretreatment measures with an approximately equal number of subjects assigned to treatment with sertraline (to a maximum of 200 mg/day) or placebo. The study will include a 14-week treatment period; because the 2 weeks are for medication taper, efficacy will be evaluated over the first 12 treatment weeks. A total of 160 early-onset or late-onset alcoholics will be randomized. Daily process measures of positive and negative events, global perceived stress, mood, desire to drink, and drinking frequency and intensity, collected using interactive voice response technology, will provide insight into the mechanisms by which sertraline may exert its effects. Coping-skills training will be provided weekly for the first 6 weeks, then every other week for the last 8 weeks of the study. A 6-month post-treatment follow-up period will evaluate the duration of medication effects. This study will also examine the relation between genotypes at a number of relevant loci and both risk of alcohol dependence and response to sertraline treatment.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Sertraline (to a maximum of 200 mg/day) for 14-week treatment period
Other names: Zoloft
Placebo for 14-week treatment period
Time frame: 12-week treatment period
Obtained using daily interactive voice response data augmented by Timeline Followback data. Missing days were treated as drinking days.
Time frame: 12-week treatment period
Obtained using daily interactive voice response data augmented by Timeline Followback data. Missing days were treated as heavy drinking days.
Time frame: 12-week treatment period compared with baseline value
Measured using the SIP (Short Inventory of Problems), which was administered at pretreatment and at the end of treatment. The range of scores on the SIP is 0 (no alcohol-related problems) to 45 (most severe alcohol-related problems) and the time frame for reporting is the preceding 3 months. The data presented here represent a difference score of treatment minus baseline.
UConn Health
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT03449095
Alcohol Drinking, Alcohol Intoxication
Champaign, Illinois, United States
View Trial DetailsNCT04210713
Alcohol Drinking, Alcohol-Related Disorders
Catonsville, Maryland, United States
View Trial DetailsNCT02885311
Alcohol Abuse, Alcohol Drinking
Great Neck, New York, United States
View Trial DetailsNCT02511808
Alcohol Abuse, Alcohol Drinking
Great Neck, New York, United States
View Trial Details