Opioid Dependence
Conditions
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.
Interventions
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).
Sponsors
Study design
Eligibility
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Number of biological samples negative/positive for opioid agonists | Week 1-12 post discharge |
| Retention | Week 1-12 post discharge |
| Days of use or abstinence from opioids | Week 1-12 post discharge |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Mental health | Week 1-12 or 1-48 | Self-reported mental health |
| Psychosocial problems | Week 1-12, Week 1-48, & Wk 49-100 | Psychosocial problems like recidivism, employment, family problems. Self-reported or registry-based. |
| Use of other substances of abuse | Week 1-48 | — |
| Somatic health | Week 1-12 or 1-48 post discharge | Self-reported and/or assessed by study personnel |
Countries
Norway