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Venlafaxine to Reduce Cocaine Dependence in Depressed Individuals

Primary Purpose

Cocaine-Related Disorders

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Venlafaxine
Placebo
Sponsored by
New York State Psychiatric Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cocaine-Related Disorders focused on measuring Cocaine Addiction, Cocaine Dependence

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Meets DSM-IV diagnosis criteria for current cocaine dependence Used cocaine at least one day in the month prior to study entry Meets DSM-IV criteria for major depression or dysthymia, with depression either primary (predates earliest life-time substance abuse), depression persistent during 6 months of cocaine abstinence in the past, or depression for at least 3 months prior to study entry If female, willing to use contraception throughout the study Exclusion Criteria: Meets DSM-IV diagnosis criteria for bipolar disorder, schizophrenia, or any psychotic disorder other than transient psychosis due to drug abuse Chronic organic mental disorder Significant risk of suicide, based on current mental state or history Untreated seizure disorder or history of substance-related seizures Unstable physical disorders that may make study participation dangerous, including hypertension, hepatitis (mildly elevated transaminase levels that are less than 4 times the upper limit or normal levels are acceptable), and diabetes Coronary vascular disease, as indicated by medical history, suspected by abnormal ECG, or history of heart symptoms Irregular heartbeat as indicated by QRS duration greater than 0.11 Current use of other prescribed psychotropic medications Currently meets DSM-IV diagnosis criteria for dependence on any drugs other than nicotine, marijuana, or alcohol History of allergic or adverse reaction to desipramine or venlafaxine Prior history of failing to respond to venlafaxine History of alcohol withdrawal syndrome in the year prior to study entry Current evidence of alcohol withdrawal, such as pulse rate greater than 115 beats per minute, blood pressure greater than 140/90 mm Hg, or visible tremors Pregnant or breastfeeding

Sites / Locations

  • New York State Psychiatric Institute

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Placebo

Venlafaxine

Arm Description

Placebo

Venlafaxine 300mg daily

Outcomes

Primary Outcome Measures

Cocaine use
Proportion of patients achieving 3 weeks of cocaine abstinence based on self report and urine toxicology
Hamilton Depression Rating Scale
Proportion of patients achieving a 50% reduction in HAM-D score at week 12 compared to baseline

Secondary Outcome Measures

Full Information

First Posted
November 3, 2005
Last Updated
July 6, 2017
Sponsor
New York State Psychiatric Institute
Collaborators
National Institute on Drug Abuse (NIDA)
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1. Study Identification

Unique Protocol Identification Number
NCT00249483
Brief Title
Venlafaxine to Reduce Cocaine Dependence in Depressed Individuals
Official Title
Placebo-Controlled Venlafaxine Treatment for Depressed Cocaine Abusers
Study Type
Interventional

2. Study Status

Record Verification Date
July 2017
Overall Recruitment Status
Completed
Study Start Date
October 1999 (undefined)
Primary Completion Date
February 2005 (Actual)
Study Completion Date
February 2005 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
New York State Psychiatric Institute
Collaborators
National Institute on Drug Abuse (NIDA)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Preliminary research has shown that venlafaxine, a medication currently used for treating depression, may also discourage cocaine use in depressed individuals. This study will evaluate the effectiveness of venlafaxine in reducing cocaine use and alleviating depression in individuals addicted to cocaine.
Detailed Description
Individuals addicted to cocaine often experience feelings of restlessness, irritability, and anxiety. They also often report feeling depressed when not using cocaine, and they tend to resume cocaine use to alleviate symptoms of depression. Venlafaxine is a medication that is currently used to treat depression and anxiety disorders. Preliminary research has shown that venlafaxine reduces depression, improves mood, and simultaneously reduces cocaine use in cocaine addicts. Further research is needed to confirm the benefits of venlafaxine for cocaine addicts. The purpose of this study is to evaluate the effectiveness of venlafaxine in reducing cocaine use, cocaine craving, and depression in individuals who are addicted to cocaine and diagnosed with depression. This study will begin with a 1-week lead-in phase, during which all participants will receive placebo medication. Participants whose depression levels decrease will not continue in the treatment phase of the study, but will be eligible for cocaine relapse therapy and medication if deemed necessary by the treating psychiatrist. Participants who remain depressed following the lead-in phase will be randomly assigned to receive either venlafaxine or placebo for 12 weeks. Participants assigned to venlafaxine will initially receive a daily dose of 37.5 mg. After 4 days, the dose will be increased to 75 mg; each week thereafter, the dose will be increased by another 75 mg, up to a maximum of 300 mg per day, dependent on side effects and positive responses. Study visits will take place twice a week. At each visit, medication side effects and depression levels will be assessed, cocaine levels will be monitored with urine tests, and self-reports will be completed. Blood will be drawn once per month for laboratory tests. Participants will also attend a therapy session once a week, and they will meet with a psychiatrist every other week for assessments. Participants who show a decrease in depression during the 12 weeks of treatment will continue for an additional 12 weeks to further monitor cocaine use and depression levels.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cocaine-Related Disorders
Keywords
Cocaine Addiction, Cocaine Dependence

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
150 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo
Arm Title
Venlafaxine
Arm Type
Experimental
Arm Description
Venlafaxine 300mg daily
Intervention Type
Drug
Intervention Name(s)
Venlafaxine
Intervention Description
Venlafaxiine 300mg/day
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
Cocaine use
Description
Proportion of patients achieving 3 weeks of cocaine abstinence based on self report and urine toxicology
Time Frame
baseline compared to 12 weeks of study or length of participation
Title
Hamilton Depression Rating Scale
Description
Proportion of patients achieving a 50% reduction in HAM-D score at week 12 compared to baseline
Time Frame
baseline compared to week 12 or last week of study participation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Meets DSM-IV diagnosis criteria for current cocaine dependence Used cocaine at least one day in the month prior to study entry Meets DSM-IV criteria for major depression or dysthymia, with depression either primary (predates earliest life-time substance abuse), depression persistent during 6 months of cocaine abstinence in the past, or depression for at least 3 months prior to study entry If female, willing to use contraception throughout the study Exclusion Criteria: Meets DSM-IV diagnosis criteria for bipolar disorder, schizophrenia, or any psychotic disorder other than transient psychosis due to drug abuse Chronic organic mental disorder Significant risk of suicide, based on current mental state or history Untreated seizure disorder or history of substance-related seizures Unstable physical disorders that may make study participation dangerous, including hypertension, hepatitis (mildly elevated transaminase levels that are less than 4 times the upper limit or normal levels are acceptable), and diabetes Coronary vascular disease, as indicated by medical history, suspected by abnormal ECG, or history of heart symptoms Irregular heartbeat as indicated by QRS duration greater than 0.11 Current use of other prescribed psychotropic medications Currently meets DSM-IV diagnosis criteria for dependence on any drugs other than nicotine, marijuana, or alcohol History of allergic or adverse reaction to desipramine or venlafaxine Prior history of failing to respond to venlafaxine History of alcohol withdrawal syndrome in the year prior to study entry Current evidence of alcohol withdrawal, such as pulse rate greater than 115 beats per minute, blood pressure greater than 140/90 mm Hg, or visible tremors Pregnant or breastfeeding
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Herbert Kleber, MD
Organizational Affiliation
New York State Psychiatric Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
New York State Psychiatric Institute
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States

12. IPD Sharing Statement

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Venlafaxine to Reduce Cocaine Dependence in Depressed Individuals

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