CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 166 enrolled
Drug / intervention
Naltrexone intramuscular suspension +1 moredrug
Likely dose
Naltrexone intramuscular suspension 380 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01717963
NCT01717963Phase 3Completed

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

University of Oslo·interventional·Posted Oct 31, 2012·Updated Oct 11, 2018

In Brief

A Phase 3 clinical trial evaluating Naltrexone intramuscular suspension and Buprenorphine-naloxone for Opioid Dependence. Completed, enrolled 166 participants across 5 sites.

Detailed 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 Details

Timeline

Phase 3CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedOct 31, 2012
Enrollment StartOct 1, 2012
Primary CompletionAug 31, 2016
Study CompletionApr 30, 2018
TodayJul 2, 2026
Enrollment to primary: 3.9 yearsPosted 13.7 years ago

Interventions

Naltrexone intramuscular suspensiondrug

A standard dosage of 380 mg / month of naltrexone intramuscular suspension will be administered

Buprenorphine-naloxonedrug

Buprenorphine-naloxone is administered daily and provided in accordance with existing guidelines for OMT in Norway (treatment-as-usual).