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Naltrexone and Adrenergic Agents to Reduce Heroin Use in Heroin Addicts

Primary Purpose

Heroin Dependence

Status
Completed
Phase
Phase 2
Locations
Russian Federation
Study Type
Interventional
Intervention
Naltrexone
Placebo
Sponsored by
Baylor College of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Heroin Dependence focused on measuring Heroin Abuse, Heroin Addiction

Eligibility Criteria

18 Years - 40 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Current primary diagnosis of heroin dependence, for at least 1 year prior to study entry High school graduate or higher education level Abstinence from drugs and alcohol for at least 1 week prior to study entry Negative urine and breathalyzer tests for alcohol and drugs No evidence of opioid dependence following narcan challenge At least one relative willing to participate in treatment, monitor administration of medications, assist in follow-up, and provide outcome data Stable address within St. Petersburg or nearest districts of Leningrad Region Able to provide a home telephone number where the participant may be reached If female, willing to use effective contraception throughout the study Exclusion Criteria: Low blood pressure, as determined by sitting blood pressure less than 90/50 mm Hg Clinically significant cognitive impairment, schizophrenia, paranoid disorder, bipolar disorder, or seizure disorder Advanced brain, heart, kidney, or liver disease Active tuberculosis Current febrile illness AIDS-defining illness Significant laboratory abnormality, including severe anemia, unstable diabetes, or liver function tests greater than three times above normal Pending legal issues that may entail a jail stay during the study Currently participating in another treatment study Currently participating in another substance abuse program Current use of a psychotropic medication Pregnant Pulse rate less than 50 bpm

Sites / Locations

  • Saint Petersburg Pavlov State Medical University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Naltrexone

Placebo

Arm Description

Naltrexone Oral 50 mgs daily

1 to 1 comparison of Naltrexone to placebo

Outcomes

Primary Outcome Measures

Heroin relapse

Secondary Outcome Measures

HIV risk factors
Psychiatric symptoms (measured at Month 6, and the 3- and 6-month follow-up evaluations)
Adherence to medication
Heroin withdrawal symptoms

Full Information

First Posted
September 1, 2005
Last Updated
October 22, 2012
Sponsor
Baylor College of Medicine
Collaborators
National Institute on Drug Abuse (NIDA)
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1. Study Identification

Unique Protocol Identification Number
NCT00142948
Brief Title
Naltrexone and Adrenergic Agents to Reduce Heroin Use in Heroin Addicts
Official Title
Heroin Addiction Treatment: Naltrexone and Adrenergic Agents
Study Type
Interventional

2. Study Status

Record Verification Date
October 2012
Overall Recruitment Status
Completed
Study Start Date
February 2006 (undefined)
Primary Completion Date
May 2011 (Actual)
Study Completion Date
May 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Baylor College of Medicine
Collaborators
National Institute on Drug Abuse (NIDA)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Naltrexone is a medication that is currently used to treat drug and alcohol addiction. Guanfacine is a medication that is currently used to manage the withdrawal symptoms in individuals undergoing opioid detoxification. A combination of these two medications may be beneficial in reducing heroin use in individuals addicted to heroin. This study will evaluate the effectiveness of naltrexone and guanfacine, alone and in combination, at reducing heroin use in heroin addicts.
Detailed Description
Heroin addiction is a serious health problem with no available medical treatment for preventing relapse. Naltrexone is a medication that is currently used to treat substance addiction. It acts by blocking the "high" feeling produced by drugs and alcohol. Guanfacine, an antihypertensive medication, is currently used to manage the withdrawal symptoms in individuals undergoing opioid detoxification. While each of these medications is useful in the treatment of heroin addiction, a combination of the two drugs may be more effective than either medication alone. The purpose of this study is to compare the effectiveness of naltrexone, guanfacine, and a combination of naltrexone and guanfacine at reducing drug relapse in heroin addicts. This study will enroll individuals addicted to heroin who have completed a prior detoxification program at one of two addiction treatment hospitals in St. Petersburg, Russian Federation. Upon completing the detoxification program of 7-14 days, participants will have a period of inpatient rehabilitation. During this 3- to 4-week inpatient stabilization period, patients will be screened for study participation. Once stabilized, participants will begin the 6-month treatment phase of the study. During this phase, they will be randomly assigned to receive one of the following drug combinations on a daily basis: 50 mg of naltrexone and guanfacine placebo; 1.0 mg of guanfacine and naltrexone placebo; 50 mg of naltrexone and 1.0 mg of guanfacine; or naltrexone placebo and guanfacine placebo. All participants will have a designated family member who will be responsible for supervising medication compliance. Study visits will occur twice monthly. Participants will receive clinical management and medication compliance counseling at each visit; family members will also take part in the counseling sessions. Outcome measurements will include drug relapse, medication adherence, withdrawal symptoms, HIV risk factors, and psychiatric symptoms. Follow-up evaluations will occur 3 and 6 months following the end of treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heroin Dependence
Keywords
Heroin Abuse, Heroin Addiction

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
301 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Naltrexone
Arm Type
Experimental
Arm Description
Naltrexone Oral 50 mgs daily
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
1 to 1 comparison of Naltrexone to placebo
Intervention Type
Drug
Intervention Name(s)
Naltrexone
Intervention Description
naltrexone
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
placebo
Primary Outcome Measure Information:
Title
Heroin relapse
Time Frame
duration of study
Secondary Outcome Measure Information:
Title
HIV risk factors
Time Frame
baseline
Title
Psychiatric symptoms (measured at Month 6, and the 3- and 6-month follow-up evaluations)
Time Frame
months 6 and the 3- and 6-month follow-up evaluations
Title
Adherence to medication
Time Frame
duration of study
Title
Heroin withdrawal symptoms
Time Frame
Month 6, and 3- and 6-month followup

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Current primary diagnosis of heroin dependence, for at least 1 year prior to study entry High school graduate or higher education level Abstinence from drugs and alcohol for at least 1 week prior to study entry Negative urine and breathalyzer tests for alcohol and drugs No evidence of opioid dependence following narcan challenge At least one relative willing to participate in treatment, monitor administration of medications, assist in follow-up, and provide outcome data Stable address within St. Petersburg or nearest districts of Leningrad Region Able to provide a home telephone number where the participant may be reached If female, willing to use effective contraception throughout the study Exclusion Criteria: Low blood pressure, as determined by sitting blood pressure less than 90/50 mm Hg Clinically significant cognitive impairment, schizophrenia, paranoid disorder, bipolar disorder, or seizure disorder Advanced brain, heart, kidney, or liver disease Active tuberculosis Current febrile illness AIDS-defining illness Significant laboratory abnormality, including severe anemia, unstable diabetes, or liver function tests greater than three times above normal Pending legal issues that may entail a jail stay during the study Currently participating in another treatment study Currently participating in another substance abuse program Current use of a psychotropic medication Pregnant Pulse rate less than 50 bpm
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Thomas R. Kosten, MD
Organizational Affiliation
Baylor College of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Saint Petersburg Pavlov State Medical University
City
Saint Petersburg
Country
Russian Federation

12. IPD Sharing Statement

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Naltrexone and Adrenergic Agents to Reduce Heroin Use in Heroin Addicts

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