The Use of Anticonvulsants for Treatment of Patients With Alcohol Dependence and Post Traumatic Stress Disorder - Full Text View

Sponsor:	Yale University
Information provided by:	Yale University
ClinicalTrials.gov Identifier:	NCT00571246

Purpose

The objective of this study is to evaluate the efficacy of topiramate (250mg) or lamotrigine (250mg) versus placebo in reducing alcohol consumption and decreasing symptoms of PTSD in patients with comorbid AD and PTSD.

Condition	Intervention	Phase
Alcohol Dependence Post Traumatic Stress Disorder	Drug: lamotrigine and topiramate	Phase III

Study Type:	Interventional
Study Design:	Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator), Placebo Control, Factorial Assignment, Safety/Efficacy Study
Official Title:	The Use of Anticonvulsants for Treatment of Patients With Alcohol Dependence and Post Traumatic Stress Disorder

Resource links provided by NLM:

MedlinePlus related topics: Alcoholism Post-Traumatic Stress Disorder

Drug Information available for: Ethanol Lamotrigine Topiramate

U.S. FDA Resources

Further study details as provided by Yale University:

Primary Outcome Measures:

drinking - measured using the TLFB [ Time Frame: 16 weeks ] [ Designated as safety issue: Yes ]
craving - measured using the OCDS [ Time Frame: 16 weeks ] [ Designated as safety issue: No ]
PTSD symptoms - measured using the CAPS [ Time Frame: 16 weeks ] [ Designated as safety issue: Yes ]

Estimated Enrollment:	90
Study Start Date:	June 2009
Estimated Study Completion Date:	June 2010
Estimated Primary Completion Date:	June 2010 (Final data collection date for primary outcome measure)

Intervention Details:

lamotrigine (250 mg/day) 2 times a day, topiramate (250mg/day) 2 times a day, placebo

Detailed Description:

There is a high rate of comorbidity with alcohol dependence (AD) and post traumatic stress disorder (PTSD). The rates of PTSD among individuals with AD are at least twice as high as those in the general population. In addition, alcohol dependence is the most common comorbid condition in men with PTSD. Despite this, little is known about how to best treat individuals with comorbid AD and PTSD. The use of anticonvulsants represents a novel approach to treatment that may target symptoms of both AD and PTSD. Both Topiramate and Lamotrigine act on the GABAergic and glutamatergic systems. Topiramate has GABAergic effects by robustly increasing brain GABA, and antiglutamatergic effects by inhibiting glutamate function that might antagonize alcohol's rewarding effects in AD and could contribute to the regulating of reexperiencing and arousal symptoms in PTSD. Lamotrigine is a glutamate-inhibiting anticonvulsant that has shown efficacy in some dually diagnosed patients with alcohol dependence, and in patients with PTSD. Neither topiramate nor lamotrigine have been used to treat patients with comorbid PTSD and AD. Methods: Ninety men and women with a current diagnosis of AD and PTSD will be enrolled in a 16-week trial. They will be assigned, in a double-blind fashion, to either topiramate, lamotrigine or placebo. Significance: This project will be the first to compare anticonvulsants (topiramate and lamotrigine) to placebo as effective treatments for reducing alcohol consumption and PTSD symptoms in patients with AD and PTSD.

Eligibility

Ages Eligible for Study:	21 Years to 65 Years
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

Inclusion Criteria:

Males and females between the ages of 18-60 years old.
Current alcohol abuse or dependence
Current PTSD
Patients with current alcohol dependence, with at least one recent episode of heavy drinking (defined as 5 or more drinks per drinking episode) over the past 14 days, and during a consecutive 30-day period within the 90 days prior to baseline evaluation.
Individuals who are on a stable dose (no less than 2 weeks) of antidepressant medication.
Medically and neurologically healthy on the basis of history, physical examination, EKG, screening laboratories (CBC w/ differential, TSH, Free-T4, ASAT, ALAT, GGT, BUN, creatinine, calcium, phosphorous, magnesium, total protein, albumin, electrolytes, VDRL, urinalysis, beta-HCG)
For women, negative pregnancy test and use of acceptable method of contraception.

Exclusion Criteria:

Females who are pregnant or lactating.
Individuals with a current unstable medical condition such as neurological, cardiovascular, endocrine, renal, liver, or thyroid pathology (LFT > 3 times normal, abnormal BUN and creatinine, and unmanaged hypertension with BP > 200/120) which in the opinion of the physician would preclude the patient from fully cooperating or be of potential harm during the course of the study (includes those with a history of glaucoma, prostatic hypertrophy, urethral obstruction, cerebral arteriosclerosis, pyloric stenosis).
Patients who meet current SCID criteria for a major Axis I diagnosis (Bipolar Disorders, Schizophrenia and Schizophrenia-type Disorders).
History of substance dependence (other than alcohol, tobacco or cannabis) by DSM-IV criteria in the last 90 days.
Individuals taking mood stabilizers and antipsychotic medications.
Individuals with a history of allergies to topiramate or lamotrigine.

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00571246

Contacts

Contact: Elizabeth Ralevski, Ph.D.

203-932-5711 ext 4282

elizabeth.ralevski@yale.edu

Locations

United States, Connecticut
VA Connecticut Healthcare System
West Haven, Connecticut, United States, 06516

Sponsors and Collaborators

Yale University

Investigators

Principal Investigator:

Ismene L Petrakis, MD

VA Connecticut Healthcare System

More Information

No publications provided

Responsible Party:	Yale University ( Ismene Petrakis )
Study ID Numbers:	00030, 0705002634
Study First Received:	December 7, 2007
Last Updated:	August 28, 2008
ClinicalTrials.gov Identifier:	NCT00571246 History of Changes
Health Authority:	United States: Institutional Review Board

Keywords provided by Yale University:

treatment
Lamotrigine
Topiramate
alcohol dependence
post traumatic stress disorder

Additional relevant MeSH terms:

Molecular Mechanisms of Pharmacological Action
Physiological Effects of Drugs
Disorders of Environmental Origin
Calcium Channel Blockers
Neuroprotective Agents
Stress Disorders, Traumatic
Membrane Transport Modulators
Pathologic Processes
Mental Disorders
Therapeutic Uses
Substance-Related Disorders
Topiramate
Stress Disorders, Post-Traumatic

Alcohol-Related Disorders
Disease
Stress
Cardiovascular Agents
Protective Agents
Pharmacologic Actions
Anti-Obesity Agents
Anxiety Disorders
Alcoholism
Lamotrigine
Central Nervous System Agents
Anticonvulsants

ClinicalTrials.gov processed this record on November 09, 2009