Optimal Prevention of Overdose Deaths and Opioid Relapse Following Discharge: A Multi-Center RCT of Naltrexone Versus Buprenorphine in Norway
Trial Snapshot
- Phase
- Phase 3
- Status
- Completed
- Sponsor
- University of Oslo
- 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
Extended release naltrexone injections 380mg
Intervention: Naltrexone intramuscular suspension (Drug)
Buprenorphine-naloxone
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
Lars Tanum
National Coordinating Investigator (PI)
University of Oslo
