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Naltrexone vs Buprenorphine-Naloxone for Opioid Dependence in Norway

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

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01717963
Acronym
NTX-SBX
Enrollment
166
Registered
2012-10-31
Start date
2012-10-31
Completion date
2018-04-30
Last updated
2018-10-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Opioid Dependence

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

DRUGNaltrexone intramuscular suspension

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

The Research Council of Norway
CollaboratorOTHER
The Royal Norwegian Ministry of Health
CollaboratorOTHER
Norwegian Institute of Public Health
CollaboratorOTHER_GOV
Oslo University Hospital
CollaboratorOTHER
University Hospital, Akershus
CollaboratorOTHER
Haukeland University Hospital
CollaboratorOTHER
Helse Stavanger HF
CollaboratorOTHER_GOV
The Hospital of Vestfold
CollaboratorOTHER
Ostfold Hospital Trust
CollaboratorOTHER
University of Oslo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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

Design outcomes

Primary

MeasureTime frame
Number of biological samples negative/positive for opioid agonistsWeek 1-12 post discharge
RetentionWeek 1-12 post discharge
Days of use or abstinence from opioidsWeek 1-12 post discharge

Secondary

MeasureTime frameDescription
Mental healthWeek 1-12 or 1-48Self-reported mental health
Psychosocial problemsWeek 1-12, Week 1-48, & Wk 49-100Psychosocial problems like recidivism, employment, family problems. Self-reported or registry-based.
Use of other substances of abuseWeek 1-48
Somatic healthWeek 1-12 or 1-48 post dischargeSelf-reported and/or assessed by study personnel

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 13, 2026