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Clinical Trials/NCT01717963
NCT01717963CompletedPhase 3

Optimal Prevention of Overdose Deaths and Opioid Relapse Following Discharge: A Multi-Center RCT of Naltrexone Versus Buprenorphine in Norway

University of Oslo5 sites in 1 country166 target enrollmentStarted: October 2012Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Phase 3
Status
Completed
Enrollment
166
Locations
5
Primary Endpoint
Number of biological samples negative/positive for opioid agonists

Study Overview

Brief Summary

Persons dependent on opioids like heroin, morphine, or codeine have a high risk of relapse, overdose and overdose death. This risk is elevated even further following discharge from treatment or correctional institutions where patients have been detoxified. At the moment, state-of-the-art treatment is based on maintaining the dependence on opioids by daily intake of opioid medications like methadone or buprenorphine. Recently, a medication containing the blocking agent naltrexone was approved in the US; this does not maintain dependence but instead blocks heroin and other opioids for 28 days after intramuscular administration. This study will conduct a 12-week randomized comparison of naltrexone intramuscular suspension (XL-NTX) with daily buprenorphine-naloxone in OMT. Medication will start preceding discharge from a treatment or correctional facility to participating catchment regions in Norway. The main hypotheses are that XL-NTX will do equally well as - or better than - OMT on the proportion of biological samples negative for opioids, retention, self-reported use of alcohol and illicit drugs. Following the 12-week randomized period, there will be a 36-week period where participants can receive the study medication of their choice. After the end of the study, data from national registry databases can be collected for a further 12 months on outcomes such as recidivism, mortality and morbidity.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Opioid dependence (DSM-IV TR)
  • Age 18 or above
  • Applied & Approved for Norway's national OMT program
  • Discharge within 30 days of inclusion from a controlled environment; e.g. inpatient treatment or correctional (prison) facility
  • Voluntarily seeking treatment for opioid dependence

Exclusion Criteria

  • Pregnant or breast-feeding
  • Acute or recurring severe psychiatric disorder, e.g. psychosis, suicidality
  • Serious debilitation of liver or renal function (e.g. Child-Pugh level C)
  • Use of excluded medication
  • Known intolerance to study drugs or their ingredients
  • Employment in firm manufacturing one of the study drugs or close relation to such person

Arms & Interventions

Naltrexone intramuscular suspension

Experimental

Extended release naltrexone injections 380mg

Intervention: Naltrexone intramuscular suspension (Drug)

Buprenorphine-naloxone

Active Comparator

Flexible oral dose 4-24 mg daily

Intervention: Buprenorphine-naloxone (Drug)

Outcomes

Primary Outcomes

Number of biological samples negative/positive for opioid agonists

Time Frame: Week 1-12 post discharge

Retention

Time Frame: Week 1-12 post discharge

Days of use or abstinence from opioids

Time Frame: Week 1-12 post discharge

Secondary Outcomes

  • Mental health(Week 1-12 or 1-48)
  • Somatic health(Week 1-12 or 1-48 post discharge)
  • Use of other substances of abuse(Week 1-48)
  • Psychosocial problems(Week 1-12, Week 1-48, & Wk 49-100)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Lars Tanum

National Coordinating Investigator (PI)

University of Oslo

Study Sites (5)

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