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 Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
166
A standard dosage of 380 mg / month of naltrexone intramuscular suspension will be administered
Buprenorphine-naloxone is administered daily and provided in accordance with existing guidelines for OMT in Norway (treatment-as-usual).
Akershus University Hospital
Oslo, Akershus, Norway
Haukeland University Hospital
Bergen, Hordaland, Norway
Stavanger University Hospital
Stavanger, Rogaland, Norway
Vestfold Hospital Trust
Tønsberg, Vestfold, Norway
Oslo University Hospital, Avdeling for Rus og Avhengighet
Oslo, Norway
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
Use of other substances of abuse
Time frame: Week 1-48
Mental health
Self-reported mental health
Time frame: Week 1-12 or 1-48
Somatic health
Self-reported and/or assessed by study personnel
Time frame: Week 1-12 or 1-48 post discharge
Psychosocial problems
Psychosocial problems like recidivism, employment, family problems. Self-reported or registry-based.
Time frame: Week 1-12, Week 1-48, & Wk 49-100
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