Neuromodulation of Trauma Memories in PTSD & Alcohol Dependence

Study Results

Results available

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE2

Total Enrollment

44 participants

Study Classification

INTERVENTIONAL

Study Start Date

2010-01-31

Study Completion Date

2012-08-31

Brief Summary

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The purpose of this study is to examine the effect of propranolol versus placebo on craving, distress and cue reactivity to trauma and alcohol cues.

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Detailed Description

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Summary and Synthesis: Epidemiological studies have established the occurrence of high rates of AD in persons with PTSD. Likewise, studies of alcohol/drug abuse treatment seekers have documented high rates of trauma exposure and PTSD. The high prevalence of PTSD/AD comorbidity is the cause of enormous human suffering, most of which either goes untreated or is resistant to treatment efforts. Both theory and research concerning the interface between these two disorders suggests that PTSD is associated with the initiation of excessive alcohol use and/or the development of AD by way of an escape/avoidance behavioral mechanism wherein escalating alcohol use is reinforced by its ability to dampen the negative emotions and arousal associated with PTSD. If PTSD is often a primary cause of the initiation and maintenance of AD, then clinical interventions that primarily impact PTSD should lead to significant improvements in craving for, and use of, alcohol. The findings of two recent treatment studies offer especially compelling support for this expectation. Drawing on both basic neuroscience research and a developing body of suggestive clinical/applied research, we were led to consider if the putative memory modulating properties of the adrenergic antagonist propranolol might have therapeutic benefits for PTSD/AD comorbid individuals. Thus, the proposed study will test the hypothesis that the strategic administration of propranolol coupled with the elicitation/retrieval of trauma-related memories will dampen emotional distress, alcohol craving and cue reactivity during subsequent exposure to trauma- and alcohol-related cues. A two-week follow-up laboratory session and clinical assessment will permit us to evaluate whether treatment benefits are maintained over time and if there are any changes in alcohol use and PTSD symptomatology.

Conditions

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Alcohol Dependence PTSD

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors

Study Groups

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Propranolol

Patients will receive Propranolol in this condition.

Group Type ACTIVE_COMPARATOR

Propranolol

Intervention Type DRUG

40 mg; Single Administration.

Placebo

Patient to receive placebo in this condition.

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DRUG

40 mg; Single Dose.

Interventions

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Propranolol

40 mg; Single Administration.

Intervention Type DRUG

Placebo

40 mg; Single Dose.

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Participants must meet DSM-IV criteria for current alcohol dependence
* Participants must have experienced criminal victimization
* Use of birth control by female participants
* Live within a 50-mile radius of research site
* Consent to remain abstinent of all drugs and alcohol for 24 hours prior to patient admission and follow-up
* Consent to random assignment to propanol or placebo
* Individuals must be able to provide informed consent and function at an intellectual level sufficient to allow accurate completion of all assessment instruments.

Exclusion Criteria

* Women who are pregnant, nursing or are of childbearing potential and not using birth control.
* Evidence or history of significant hematological, endocrine, cardiovascular, pulmonary, renal, gastrointestinal or neurological disease
* Significant liver impairment
* Currently taking anti-arrhythmic agents, psychostimulants or other agents known to interfere with heart rate and skin conductance monitoring.
* Known or suspected hypersensitivity to propanol
* Individuals taking medication that could adversely interact with the study medication, including the following: albuterol, insulin or significant inhibitors of CYP2D6
* Individuals with bronchial asthma or chronic obstructive pulmonary disease
* Prospective participants will be excluded if they are currently receiving exposure-based therapy for PTSD.
* Individuals with a history of or current psychotic disorder.
* Individuals with Addison's disease, Cushing's disease or other diseases of the adrenal cortex likely to affect cortisol levels.
* Individuals receiving synthetic glucocorticoid therapy, any exogenous therapy, or treatment with other agents that interfere with HPA axis function within one month of the time of testing.
* Individuals with resting heart rates less than 55 bpm.

Minimum Eligible Age

18 Years

Maximum Eligible Age

100 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes