Understanding Treatment Response With Naltrexone Among White Alcoholics

NCT ID: NCT00817089

Last Updated: 2019-11-21

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 24 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2007-12-31
• Study Completion Date: 2010-06-30

Brief Summary

This is a study involving treatment for alcohol dependence among males of European or Asian decent. The ultimate aim of this line of investigation is to further establish a genetic link between alcohol dependence and treatment by defining an endophenotype associated with treatment response. The study consists of two inpatient alcohol challenge sessions with treatment using random assignment to either naltrexone or placebo.

Detailed Description

Despite the well-established efficacy of naltrexone, there are significant variations in individual responses to naltrexone. A critical question remains: under what circumstances and for which patients will naltrexone be most beneficial? Recent work at our center provides evidence that the mu-opioid receptor (OPRM1) gene polymorphism A118G (Asn40Asp) imparts a significant change in treatment response. We have shown that patients with Asn40 variant (absence of heavy drinking -73.9% v/s 49% response). To further consolidate our knowledge, we wish to test the relationship between A118G polymorphism and the subjective/objective measures to alcohol among alcoholics treated with naltrexone. This work is focused on subjects of European or Asian decent as the A118G polymorphism occurs in less than 1% of those of African decent.

Up to 40 subjects will be recruited. The subjects were admitted to the UPenn Translational Research Center and receive two alcohol challenge sessions after pretreatment with naltrexone or placebo.

Conditions

Alcoholism

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Group 1 Asn40 Placebo Placebo

Each alcohol session preceded by pretreatment with placebo oral tablet

Group Type: PLACEBO_COMPARATOR

Placebo Oral Tablet

Intervention Type: DRUG

Placebo pill

Group 2 Asn40 Placebo Naltrexone

The first alcohol session preceded by pretreatment with placebo oral tablet. The second alcohol session preceded by pretreatment with naltrexone 50 mg as a single dose.

Group Type: ACTIVE_COMPARATOR

Placebo Oral Tablet

Intervention Type: DRUG

Placebo pill

Naltrexone

Intervention Type: DRUG

50 mg of naltrexone prior to challenge session

Group 3 Asp40 Placebo Placebo

Each alcohol session preceded by pretreatment with placebo oral tablet

Group Type: PLACEBO_COMPARATOR

Placebo Oral Tablet

Intervention Type: DRUG

Placebo pill

Group 4 Asp40 Placebo Naltrexone

The first alcohol session preceded by pretreatment with placebo oral tablet. The second alcohol session preceded by pretreatment with naltrexone 50 mg as a single dose.

Group Type: ACTIVE_COMPARATOR

Placebo Oral Tablet

Intervention Type: DRUG

Placebo pill

Naltrexone

Intervention Type: DRUG

50 mg of naltrexone prior to challenge session

Interventions

Placebo Oral Tablet

Placebo pill

Intervention Type: DRUG

Naltrexone

50 mg of naltrexone prior to challenge session

Intervention Type: DRUG

Other Intervention Names

Placebo

Eligibility Criteria

Inclusion Criteria

1. Males 21 years of age or older of European or Asian decent.

2. Has a current DSM IV diagnosis of alcohol dependence as determined by the Structural Clinical Interview for DSM IV (SCID-IV Mini).

3. Drank an average of 21 drinks/week in the 60 days prior to treatment and had at least 2 occasions of heavy drinking (5 or more drinks on a given day for men), as measured by the Timeline Followback (TLFB).

4. Has adequate vision, hearing, and ability to communicate to allow study participation.

5. Successfully completes detoxification as manifested by at least 48 consecutive hours of no self-reported alcohol use immediately prior to admission to the inpatient unit.

6. Has signed a witnessed informed consent

7. Scores below an 8 on the Clinical Inventory of Withdrawal for Alcohol (CIWA) prior to starting naltrexone/placebo; and 8) Can speak, print, and understand English.

Exclusion Criteria

1. Meets DSM-IV criteria for dependence on any substance other than alcohol or nicotine in the last 6 months.

2. Tests positive on the urine drug screen for opioids, cocaine, or amphetamine at the screening visit (only 1 repeat test permitted).

3. Meets current or lifetime DSM-IV criteria for bipolar affective disorder, schizophrenia, or any psychotic disorder

4. The presence of unstable or serious medical illness, including history of stroke, seizure disorder, severe liver disease (AST or ALT > 5x normal at the time of randomization), or unstable cardiac disease

5. Has taken any psychotropic medications (including disulfiram) regularly within the last seven days prior to randomization (14 days for fluoxetine) or needs immediate treatment with a psychotropic medication (with the exception of detoxification medications or benadryl used sparingly for sleep)

6. Over age 64 and has evidence of severe cognitive impairment as evidenced by a Mini-mental status exam (MMSE) score <24

7. Has suicidal or homicidal ideation necessitating inpatient hospitalization

8. Has been abstinent more than 14 days prior to Phase 1

9. Is of African Descent

10. Meets current DSM-IV criteria for for major depression (non-substance induced), PTSD, or panic disorder.

11. Has significant hematological, pulmonary, endocrine, cardiovascular, renal, or gastrointestinal disease.

• Minimum Eligible Age: 21 Years
• Maximum Eligible Age: 64 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

University of Pennsylvania

OTHER

Sponsor Role: lead

Responsible Party

David Oslin

Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

David Oslin, M.D.

Role: PRINCIPAL_INVESTIGATOR

University of Pennsylvania

Locations

University of Pennsylvania

Philadelphia, Pennsylvania, United States

Countries

United States

Other Identifiers

806019

Identifier Type: -

Identifier Source: org_study_id