Naltrexone intramuscular suspension
DrugA standard dosage of 380 mg / month of naltrexone intramuscular suspension will be administered
Other names: Long-acting naltrexone, Extended-release naltrexone, XR-NTX, Vivitrol
NCT Number: NCT01717963
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.
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Notify Me18 year and older
All sexes
Interventional
Phase 3
Akershus University Hospital, Oslo, Akershus, Norway
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
A standard dosage of 380 mg / month of naltrexone intramuscular suspension will be administered
Other names: Long-acting naltrexone, Extended-release naltrexone, XR-NTX, Vivitrol
Buprenorphine-naloxone is administered daily and provided in accordance with existing guidelines for OMT in Norway (treatment-as-usual).
Other names: Suboxone
Time frame: Week 1-12 post discharge
Time frame: Week 1-12 post discharge
Time frame: Week 1-12 post discharge
Time frame: Week 1-48
Time frame: Week 1-12 or 1-48
Self-reported mental health
Time frame: Week 1-12 or 1-48 post discharge
Self-reported and/or assessed by study personnel
Time frame: Week 1-12, Week 1-48, & Wk 49-100
Psychosocial problems like recidivism, employment, family problems. Self-reported or registry-based.
University of Oslo
Other
Optimal Prevention of Overdose Deaths and Opioid Relapse Following Discharge: A Multi-Center RCT of Naltrexone Versus Buprenorphine in Norway
Acronym: NTX-SBX
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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