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Trial of Seroquel SR for Alcohol Dependence and Comorbid Anxiety

Primary Purpose

Alcoholism, Anxiety Disorders, Generalized Anxiety Disorder

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Seroquel XR
Sponsored by
Creighton University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Alcoholism focused on measuring Alcoholism, Anxiety, GAD, PTSD, Panic Disorder, OCD

Eligibility Criteria

19 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Diagnosis of alcohol dependence and an anxiety disorder (generalized anxiety disorder, post traumatic disorder, panic disorder, obsessive compulsive disorder, etc.) based on Mini-International Neuropsychiatric Interview (MINI) for DSM IV. Subject reports a minimum of 48 standard alcoholic drinks (or an average of 12 drinks/wk) in a consecutive 30-day period (i.e., a minimum of 40% days drinking), and has 2 or more days of heavy drinking (defined as ≥5 drinks/day in males and ≥4 drinks/day in females) in this same period as measured by the Time Line Follow Back. Male and female patients between 19-65 years of age. Ability to provide informed consent. Medically and psychiatrically stable defined as not requiring inpatient treatment. Exclusion Criteria: Inability to provide informed consent. Need for inpatient treatment Need for inpatient detoxification for substance other than alcohol Evidence of active dependence on a substance other than alcohol (with the exception of nicotine) as assessed by a urine drug screen. Medically or psychiatrically unstable patients, defined as requiring inpatient treatment. Pregnancy, nursing or refusal to use a reliable method of birth control in women. Current treatment with other antipsychotic medications, which cannot be switched to Seroquel SR. Patients with known allergy to Seroquel IR/SR or treatment failure to Seroquel IR/SR. Exclude patients (pts) with unstable diabetes. Exclude pts over 65 Exclude pts with dementia

Sites / Locations

  • Creighton University Department of Psychiatry

Arms of the Study

Arm 1

Arm Type

Placebo Comparator

Arm Label

2

Arm Description

Subjects will be randomized to receive either Seroquel SR or placebo

Outcomes

Primary Outcome Measures

Aim 1: To determine whether Seroquel SR reduces alcohol use and prolongs sobriety as measured by the Time Line Follow Back Method and breathalyzer test in individuals with alcohol dependence and co-morbid anxiety.

Secondary Outcome Measures

Aim 2: To determine whether Seroquel SR decreases craving as measured by the Pennsylvania Craving Scale, in individuals with alcohol dependence and co-morbid anxiety.
Aim 3: To determine whether Seroquel SR reduces anxiety symptoms as measured by the Hamilton Rating Scale for Anxiety (HAM-A), in individuals with alcohol dependence and co-morbid anxiety.

Full Information

First Posted
July 12, 2006
Last Updated
December 5, 2008
Sponsor
Creighton University
Collaborators
AstraZeneca
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1. Study Identification

Unique Protocol Identification Number
NCT00352469
Brief Title
Trial of Seroquel SR for Alcohol Dependence and Comorbid Anxiety
Official Title
12 Week Prospective Double Blind Placebo Controlled Randomized Trial of Seroquel SR for Alcohol Dependence and Comorbid Anxiety
Study Type
Interventional

2. Study Status

Record Verification Date
December 2008
Overall Recruitment Status
Completed
Study Start Date
February 2006 (undefined)
Primary Completion Date
November 2008 (Actual)
Study Completion Date
November 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Creighton University
Collaborators
AstraZeneca

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Alcohol use disorders (AUDs) are a major problem facing our society. Their treatment is complex, and involves multiple behavioral and pharmacotherapy interventions. There are 3 approved medications for AUDs, but their efficacy for AUDs that co-exist with anxiety disorders is unknown. This study explores the effects of the medication, sustained-release quetiapine fumarate (Seroquel SR) for the treatment of alcohol dependence and co-morbid anxiety. Primary outcome measure is the amount of alcohol used. Secondary outcome measures include craving for alcohol, length of sobriety from drinking and level of anxiety with Seroquel SR.
Detailed Description
STUDY OBJECTIVES: The objective of this proposal is to study the efficacy of the medication Seroquel SR for the treatment of alcohol dependence and co-morbid anxiety in a prospective double blind placebo-controlled randomized clinical study. Patients, meeting the DSM-IV criteria for Alcohol Dependence and an Anxiety Disorder, will be enrolled and randomized to receive placebo or Seroquel SR. All subjects will be referred to usual treatment program, where they can receive group/self help group therapy. Method: This is a 12-week prospective, double blind placebo-controlled randomized clinical trial of Seroquel SR in patients who meet the Diagnostic and Statistical Manual of Psychiatric Disorders (DSM-IV) criteria for alcohol dependence and anxiety disorders. Potential candidates will be allowed sufficient time to review the consent document and ask questions about the trial prior to signing the consent document. Consenting adults will be randomized to receive active medication, Seroquel SR or placebo for 12-weeks. The study will enroll 20 patients, 10 will be randomized to receive Seroquel SR, and 10 will receive placebo. All participants will also be referred to usual alcohol treatment, including individual, group and/or self help group therapy (Alcoholics Anonymous). Subjects will be randomized to receive either Seroquel SR or placebo. Dosing of Seroquel SR will occur on the following schedule: At the baseline visit, Seroquel SR will be started at 50 mg QHS for Day 1 and 2, and dose increase to 150 mg QHS on day 3-4, and increased further to 300 mg QHS from day 5-day 42. After day 5, the Seroquel SR dosage can be increased by up to 100 mg per week to a maximal dose of 400 mg per day. During the treatment period, dose reductions (because of physical illness or adverse event) are allowed for patients taking at least 200 mg per day.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alcoholism, Anxiety Disorders, Generalized Anxiety Disorder, Post-Traumatic Stress Disorder, Panic Disorder, Obsessive-Compulsive Disorder
Keywords
Alcoholism, Anxiety, GAD, PTSD, Panic Disorder, OCD

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
2
Arm Type
Placebo Comparator
Arm Description
Subjects will be randomized to receive either Seroquel SR or placebo
Intervention Type
Drug
Intervention Name(s)
Seroquel XR
Intervention Description
Day 1 and 2 Seroquel XR 50 mg; Day 3-4 Seroquel XR 150mg;Day 5-42 Seroquel XR 300-400mg
Primary Outcome Measure Information:
Title
Aim 1: To determine whether Seroquel SR reduces alcohol use and prolongs sobriety as measured by the Time Line Follow Back Method and breathalyzer test in individuals with alcohol dependence and co-morbid anxiety.
Time Frame
Two Years
Secondary Outcome Measure Information:
Title
Aim 2: To determine whether Seroquel SR decreases craving as measured by the Pennsylvania Craving Scale, in individuals with alcohol dependence and co-morbid anxiety.
Time Frame
Two Years
Title
Aim 3: To determine whether Seroquel SR reduces anxiety symptoms as measured by the Hamilton Rating Scale for Anxiety (HAM-A), in individuals with alcohol dependence and co-morbid anxiety.
Time Frame
Two years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
19 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of alcohol dependence and an anxiety disorder (generalized anxiety disorder, post traumatic disorder, panic disorder, obsessive compulsive disorder, etc.) based on Mini-International Neuropsychiatric Interview (MINI) for DSM IV. Subject reports a minimum of 48 standard alcoholic drinks (or an average of 12 drinks/wk) in a consecutive 30-day period (i.e., a minimum of 40% days drinking), and has 2 or more days of heavy drinking (defined as ≥5 drinks/day in males and ≥4 drinks/day in females) in this same period as measured by the Time Line Follow Back. Male and female patients between 19-65 years of age. Ability to provide informed consent. Medically and psychiatrically stable defined as not requiring inpatient treatment. Exclusion Criteria: Inability to provide informed consent. Need for inpatient treatment Need for inpatient detoxification for substance other than alcohol Evidence of active dependence on a substance other than alcohol (with the exception of nicotine) as assessed by a urine drug screen. Medically or psychiatrically unstable patients, defined as requiring inpatient treatment. Pregnancy, nursing or refusal to use a reliable method of birth control in women. Current treatment with other antipsychotic medications, which cannot be switched to Seroquel SR. Patients with known allergy to Seroquel IR/SR or treatment failure to Seroquel IR/SR. Exclude patients (pts) with unstable diabetes. Exclude pts over 65 Exclude pts with dementia
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pirzada Sattar, MD
Organizational Affiliation
Creighton University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Creighton University Department of Psychiatry
City
Omaha
State/Province
Nebraska
ZIP/Postal Code
68131
Country
United States

12. IPD Sharing Statement

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Trial of Seroquel SR for Alcohol Dependence and Comorbid Anxiety

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