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Completed

NCT Number: NCT01717963

Naltrexone vs Buprenorphine-Naloxone for Opioid Dependence in Norway

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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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Akershus University Hospital, Oslo, Akershus, Norway

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Naltrexone intramuscular suspension

Drug

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

Drug

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

Other names: Suboxone

Primary outcomes

  1. Number of biological samples negative/positive for opioid agonists

    Time frame: Week 1-12 post discharge

  2. Retention

    Time frame: Week 1-12 post discharge

  3. Days of use or abstinence from opioids

    Time frame: Week 1-12 post discharge

Secondary outcomes

  1. Use of other substances of abuse

    Time frame: Week 1-48

  2. Mental health

    Time frame: Week 1-12 or 1-48

    Self-reported mental health

  3. Somatic health

    Time frame: Week 1-12 or 1-48 post discharge

    Self-reported and/or assessed by study personnel

  4. Psychosocial problems

    Time frame: Week 1-12, Week 1-48, & Wk 49-100

    Psychosocial problems like recidivism, employment, family problems. Self-reported or registry-based.

Sponsors and collaborators

Lead sponsor

University of Oslo

Other

Collaborators

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

Registry information

Official study title

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

Acronym: NTX-SBX

Important dates

Study start
2012
Primary completion
2016
Study completion
2018
First posted
Oct 31, 2012
Registry last updated
Oct 11, 2018

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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