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Phase 3 Completed N=60 Randomized Triple-blind Treatment

Behavioral Naltrexone Therapy for Promoting Adherence to Oral Naltrexone vs Extended Release Injectable Depot Naltrexone

Opiate Dependence · Heroin Dependence
Source: ClinicalTrials.gov NCT00577408 ↗
Enrolled (actual)
60
Serious AEs
15.0%
Results posted
Aug 2017
Primary outcomePrimary: Treatment Retention — 24; 20; 17; 14 Participants
◆ Published Evidence
Emerging
5citations · ~5 / year
Sustained-release naltrexone for opioid dependence.
The Cochrane database of systematic reviews · 2025 · Open access · Likely link

Summary

In pilot study now proposed, we plan to randomly assign 60 opioid dependent patients to the new model, Depot-BNT, or to BNT plus oral naltrexone for a 6-month trial. This will provide initial clinical experience with the new Depot-BNT treatment model, while providing a rigorous test of whether Depot-BNT produces superior treatment outcome, compared to our best behavioral platform for oral naltrexone (BNT). The following aims will be addressed: Specific Aim #1: To test whether Depot-BNT increases retention in treatment and improves drug use outcome (urine-confirmed abstinent weeks) compared to our established model of BNT with oral naltrexone (BNT-Oral), and to explore whether Depot-BNT (vs BNT-Oral) improves key secondary outcomes including dysphoria, HIV risk behavior, and social functioning. Specific Aim #2: To explore predictors of outcome on Depot-BNT, and mechanisms of attrition, in order to optimize Depot-BNT prior to further testing.

Linked Publications

  • Sustained-release naltrexone for opioid dependence.
    The Cochrane database of systematic reviews · 2025 · 5 citations · Open access · Likely link

Outcome Measures

OutcomeResultp-value
PRIMARY
Treatment Retention
24; 20; 17; 14; 16; 9

Eligibility Criteria

Inclusion Criteria

  • Age 18-60.
  • Meets DSM-IV criteria for current opiate dependence disorder of at least six months duration, supported by a positive urine for opiates and a positive naloxone challenge test if the diagnosis is unclear. If participating as an outpatient only, recent opiate dependence must be confirmed by clinical history and/or communication with former treatment provider.
  • Seeking treatment for heroin dependence.
  • Able to give informed consent.

Exclusion Criteria

  • Methadone maintenance treatment or regular use of illicit methadone (> 30 mg per week).
  • Maintenance on, or regular use of buprenorphine or other long-acting narcotic agonists.
  • Pregnancy, lactation, or failure in a sexually active woman to use adequate contraceptive methods.
  • Active medical illness which might make participation hazardous, such as untreated hypertension, hepatitis with SGOT or SGPT > 3 times normal, unstable diabetes.
  • Active psychiatric disorder which might interfere with participation or make participation hazardous, including DSM-IV schizophrenia, bipolar disorder with mania or psychosis, and depressive disorder with suicide risk or 1 or more suicide attempts within the past year.
  • Physiologically dependent on alcohol or sedative-hypnotics with impending withdrawal. Other substance use diagnoses are not exclusionary. Multiple substance use is common in this population, and such an exclusion would rule out a large proportion of the population and limit the generalizability of the study.
  • History of allergic reaction to buprenorphine, naltrexone, naloxone, clonidine, or clonazepam.
  • Chronic organic mental disorder (e.g. AIDS dementia).
  • History of accidental drug overdose in the last 3 years as defined as an episode of opioid-induced unconsciousness or incapacitation, whether or not medical treatment was sought or received.
  • Currently receiving any other investigational drug, or has used any other investigational drug within 30 days of study entry.
  • Currently prescribed or regularly taking opiates for chronic pain or medical illness or those individuals anticipating surgical procedures which will necessitate opioid medications.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00577408) and the linked publication. Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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