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Completed

NCT Number: NCT01843023

Extended Release Naltrexone for Opioid-Dependent Youth

The purpose of this study is to compare 6-month treatment outcomes for 15-21 year old opioid-dependent youth receiving extended release naltrexone (XR-NTX) v. Treatment as Usual (TAU).

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Key information

Age range

15 year–21 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Friends Research Institute, Baltimore, Maryland, United States

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About this study

This proposed study is a 6-month, two-group randomized clinical trial of XR-NTX v. TAU for 340 opioid-dependent youth ages 15-21. The study will be conducted at Mountain Manor Treatment Center, a community drug treatment program in Baltimore. TAU will consist of buprenorphine treatment of opioid withdrawal followed by counseling with or without continued buprenorphine.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Meets Diagnostic and Statistical Manual-IV criteria for opioid dependence, physiologic subtype;
  • Within 3 days of admission to MMTC;
  • Age between 15 and 21, inclusive;
  • Able and willing to provide informed consent to be randomly assigned to XR- NTX or TAU; and for participants under 18 years of age, parental or guardian consent and participant assent.

Exclusion criteria

  • Liver function test levels (Alanine Transaminase, Aspartate Transaminase) four times greater than normal;
  • Unstable medical or psychiatric illness (e.g., schizophrenia) that might make participation hazardous;
  • History of serious suicide attempt in the past 6 months;
  • History of allergic reaction to naloxone, and/or naltrexone;
  • Current chronic pain condition for which opioids are deemed necessary for ongoing care;
  • blood coagulation disorder (e.g., hemophilia);
  • Body Mass Index > 40;
  • If female, pregnant, lactating, unwilling or unable (due to parental objection) to use FDA-approved contraceptive methods;
  • meeting DSM-IV criteria for benzodiazepine dependence

Treatment and study plan

Extended release naltrexone

Drug

naltrexone for extended release injectable suspension

Other names: Vivitrol

Psychosocial treatment

Behavioral

Psychosocial treatment will consist of group and individual drug abuse counseling at MMTC and in the community.

buprenorphine

Drug

Participants assigned to TAU will receive buprenorphine for opioid withdrawal and will either be tapered off the medication or will remain on it for individualized lengths of time during the six month study.

Other names: Suboxone, Subutex

Primary outcomes

  1. Opioid Use at 6 Month Follow-up

    Time frame: 6 months

    To determine the relative effectiveness of XR-NTX compared to TAU for opioid-dependent youth in terms of opioid use at 6-months post-treatment entry.

Secondary outcomes

  1. Treatment Retention

    Time frame: 6 months

    To determine the relative effectiveness of XR-NTX compared to TAU for opioid-dependent youth in terms of days in treatment. Treatment defined as medications for OUD received in past 30 days at 6-month follow-up.

  2. Monetized Healthcare Utilization

    Time frame: 6 months

    The cost-effectiveness will be assessed using the Economic Form 90 to collect data on economic outcomes of health utilization at 6 months.

  3. HIV Sex Risk Behaviors

    Time frame: 6 months

    To examine the impact of XR-NTX on HIV sex-risk behaviors at 6 months. Past 90 days self-reported HIV sex risk behaviors on the Risk Assessment Battery (RAB). Minimum value 0; maximum value 24. Higher scores reflect endorsement of more risk behaviors (worse outcome).

Sponsors and collaborators

Lead sponsor

Friends Research Institute, Inc.

Other

Collaborators

  • National Institute on Drug Abuse (NIDA)

Registry information

Official study title

Health Services Research: Extended Release Naltrexone for Opioid-Dependent Youth

Important dates

Study start
2013
Primary completion
2018
Study completion
2019
First posted
Apr 30, 2013
Registry last updated
Nov 10, 2021

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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