Status:
COMPLETED
Combined Treatment for Alcohol-Dependent Individuals With PTSD
Lead Sponsor:
New York State Psychiatric Institute
Collaborating Sponsors:
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Conditions:
Stress Disorders, Post-Traumatic
Alcohol Abuse
Eligibility:
All Genders
18-65 years
Phase:
PHASE2
Brief Summary
This treatment intervention trial is designed for men and women with either alcohol misuse (e.g. hazardous or binge drinking) or alcohol use disorders (alcohol abuse or dependence) and comorbid PTSD. ...
Detailed Description
The impetus for the current study is to contribute to the development of effective treatments targeted for men and women with either alcohol misuse (e.g., hazardous or binge drinking) or alcohol use d...
Eligibility Criteria
Inclusion
- Males and females who are a minimum of 18 years and maximum of 65 years.
- Participants meet Diagnostic and Statistical Manual Diploma in Social Medicine IV (DSM-IV) criteria for current alcohol misuse, abuse or dependence.
- Participants must have current alcohol use over past 90 days defined by more than or equal to 2 heavy drinking days or more than or equal to 14 drinks over 30 consecutive days or abstinence less than or equal to 21 consecutive days.
- Participants meet criteria for full or subthreshold PTSD. Subthreshold PTSD criteria differs from full PTSD in that the individual meets cluster C (numbing) OR cluster D (hyperarousal) whereas full PTSD requires that the individual meets both cluster C and D.
- Participants demonstrate no gross organic mental syndrome.
- Participants are capable of giving informed consent and capable of complying with study procedures.
- Participants speak English.
Exclusion
- Individuals who are at significant risk for suicide based on their current mental state or history.
- Participants with other current Axis I psychiatric disorders that, in the investigators' judgment, are unstable and would be disrupted by study medications. Current diagnosis of Bipolar I and psychotic disorders are exclusionary.
- Participants who are currently severely depressed.
- Participants with a history of psychosis or mania.
- Participants with organic mental syndrome.
- Participants physiologically dependent on any substance other than alcohol (excluding nicotine or caffeine or medically stable and managed methadone).
- Participants with comorbid substance abuse disorder who require detoxification treatment.
- Participants with unstable or significant physical disorders (e.g., uncontrolled hypertension, poorly-controlled diabetes, alanine aminotransferase/aspartate aminotransaminase (AST/ALT) three times the upper limit of normal) that would increase the risk of study participation.
- Participants with a known history of seizures (not related to alcohol withdrawal).
- Participants with moderate to severe alcohol withdrawal that would require pharmacological intervention.
- Participants currently taking prescribed psychotropic medication that is contraindicated for use with sertraline (e.g. antidepressant medications except for mirtazapine or trazodone when used for the treatment of insomnia ) and/or psychotropic medications where the participant has not achieved a stabilized regimen. Participants that are stable on medications that are not contraindicated with the use of sertraline (e.g., Methadone or Adderall) will not be excluded.
- A history of an allergic reaction to sertraline.
- Women who are currently pregnant or are trying to get pregnant or are nursing or are pre-menopausal and sexually active but not using effective birth control.
- Participants refusing to be audio or videotaped.
Key Trial Info
Start Date :
May 1 2006
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 1 2013
Estimated Enrollment :
69 Patients enrolled
Trial Details
Trial ID
NCT00262223
Start Date
May 1 2006
End Date
July 1 2013
Last Update
March 3 2020
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
City College, City University of New York
New York, New York, United States, 10031