Guanfacine to Reduce Stress-Induced Cocaine/Alcohol Craving and Relapse
Status: | Recruiting |
---|---|
Healthy: | No |
Age Range: | 18 - 50 |
Updated: | 4/21/2016 |
Start Date: | April 2006 |
End Date: | June 2016 |
Contact: | Rachel L Hart, MA |
Email: | rachel.hart@yale.edu |
Phone: | 203-737-1176 |
This study aims to test the preliminary efficacy of 3.0 mg of guanfacine (GFC) daily versus
placebo in cocaine and/or alcohol dependent individuals. This proposal is a laboratory and
treatment outcome study to examine the effects of guanfacine on brief exposure to stress,
drug cues and neutral situations on cocaine/alcohol craving, mood and neurobiological
reactivity in a sample of cocaine and/or alcohol dependent individuals. Guanfacine will be
beneficial for reduction in stress and drug cue induced craving and related arousal. In a
sample of 60 cocaine and/or alcohol dependent men and women, we propose to examine (a)
differences in measures of cocaine craving, emotion state, hypothalamic-pituitary-adrenal
(HPA) activation, physiological arousal and plasma catecholamine response to stress imagery
and to drug cue imagery as compared to neutral imagery; (b) reduction in cocaine/alcohol
abstinence symptoms; and (c) improvement in cocaine and alcohol treatment outcomes as
measured by increasing abstinence, reduction in cocaine/alcohol use and increased treatment
attendance. Hypothesis 1: Guanfacine will decrease stress-induced cocaine craving, negative
emotions and related arousal in the laboratory as compared to placebo. Hypothesis 2a: As
compared to the PLA group, the GFC group will show significant reductions in protracted
withdrawal symptoms as measured by the CSSA/CIWA during the 9-week treatment period.
Hypothesis 2b: As compared to the PLA group, a higher percentage of the GFC patients will
remain abstinent during the 9-week treatment period with a higher percent of negative
cocaine urines and alcohol-free days.
Hypothesis 2c: The GFC group will show greater adherence to treatment as measured by the
days in treatment as compared to the Pla group.
placebo in cocaine and/or alcohol dependent individuals. This proposal is a laboratory and
treatment outcome study to examine the effects of guanfacine on brief exposure to stress,
drug cues and neutral situations on cocaine/alcohol craving, mood and neurobiological
reactivity in a sample of cocaine and/or alcohol dependent individuals. Guanfacine will be
beneficial for reduction in stress and drug cue induced craving and related arousal. In a
sample of 60 cocaine and/or alcohol dependent men and women, we propose to examine (a)
differences in measures of cocaine craving, emotion state, hypothalamic-pituitary-adrenal
(HPA) activation, physiological arousal and plasma catecholamine response to stress imagery
and to drug cue imagery as compared to neutral imagery; (b) reduction in cocaine/alcohol
abstinence symptoms; and (c) improvement in cocaine and alcohol treatment outcomes as
measured by increasing abstinence, reduction in cocaine/alcohol use and increased treatment
attendance. Hypothesis 1: Guanfacine will decrease stress-induced cocaine craving, negative
emotions and related arousal in the laboratory as compared to placebo. Hypothesis 2a: As
compared to the PLA group, the GFC group will show significant reductions in protracted
withdrawal symptoms as measured by the CSSA/CIWA during the 9-week treatment period.
Hypothesis 2b: As compared to the PLA group, a higher percentage of the GFC patients will
remain abstinent during the 9-week treatment period with a higher percent of negative
cocaine urines and alcohol-free days.
Hypothesis 2c: The GFC group will show greater adherence to treatment as measured by the
days in treatment as compared to the Pla group.
Inclusion Criteria:
- Male or female individuals, ages 18 and above, meeting current DSM-IV criteria for
cocaine and/or alcohol dependence.
- COCAINE SAMPLE: meet current DSM-IV criteria for cocaine dependence; documented
positive urine toxicology screen for cocaine at intake
- ALCOHOLIC SAMPLE: meet current DSM-IV criteria for alcohol dependence
- Subject has voluntarily given informed consent and signed the informed consent
document.
- Able to read English and complete study evaluations.
Exclusion Criteria:
- Meet current criteria for dependence on another psychoactive substance, excluding
nicotine and caffeine;
- Any current use of opiates or past history of opiate abuse/dependence;
- Current use of any psychoactive drugs, including anxiolytics, antidepressants,
naltrexone or antabuse;
- Any psychotic disorder or current Axis I psychiatric symptoms requiring specific
attention, including need for psychiatric medications for current major depression
and anxiety disorders
- Significant underlying medical conditions such as cerebral, renal, thyroid or cardiac
pathology which in the opinion of study physician would preclude patient from fully
cooperating or be of potential harm during the course of the study;
- Abstinent from cocaine for more than two weeks prior to admission.
- Hypotensive individuals with sitting blood pressure below 90/50 mmHG.
We found this trial at
1
site
New Haven, Connecticut 06519
Phone: 203-737-1176
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