search
Back to results

Extended-Release Naltrexone for Opioid Relapse Prevention Following Release From Jail

Primary Purpose

Opiate Dependence

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Extended-Release Naltrexone
Motivational Enhancement Counseling
Sponsored by
NYU Langone Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Opiate Dependence focused on measuring Extended-release naltrexone, Prisoners, Opioid addiction prevention, Medication Treatment Alternatives, Prevention of Relapse to Opioid Addiction

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adults incarcerated in NYC jails with known release date
  • DSM-IV criteria for current opioid dependence
  • No current agonist (methadone, buprenorphine) treatment
  • Currently opioid free by history ('detoxed') and with a negative urine for all opioids
  • General good health as determined by complete medical interview and physical examination
  • Age 18-60 years.

Exclusion Criteria:

  • History of liver failure, cirrhosis, or recent liver function test levels greater than three times normal
  • Pregnancy, lactation, or planning conception
  • Active medical illness that might make participation hazardous
  • Untreated psychiatric disorder
  • History of allergic reaction to naltrexone, PLG (polylactide co-glycolide), carboxymethylcellulose, or any other components of the diluent.
  • Current chronic pain condition treated with opioids.

Sites / Locations

  • New York University School of Medicine
  • New York City Department of Correction

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Extended-release naltrexone (XR-NTX)

Motivational Enhancement Counseling Only

Arm Description

A single 380mg IM depot injection of XR-NTX in the week prior to release from jail. A second 380mg IM injection is offered to persons in the XR-NTX arm post-release and 4 weeks after the initial injection.

The randomized control arm receives no medication treatment and is offered brief, two-session Motivational Enhancement counseling prior to release from jail.

Outcomes

Primary Outcome Measures

Post-Release Opioid Relapse
Post-release opioid relapse at week 4, measured by self-report (Time Line Follow Back) and urine toxicologies, and defined as ≥10 of 28 days of self-reported opioid misuse following jail release or two or three positive of the three urine samples during weeks 2, 3 and 4. A single positive or missing urine result counted as 7 opioid misuse days.

Secondary Outcome Measures

Participation in Community Drug Treatment Post-release
This secondary outcome tracks community drug treatment initiation four weeks post-release from jail. Measured by self-report community drug treatment initiation at week 4 study visit.
Any Opioid Use Post-release
Counts of any opioid use, defined as self-reported ≥ 1 day of heroin or other opioid use as measured by the Timeline Follow-Back assessment during the first 4 weeks post-release.
Injection Drug Use Post-release
This secondary outcome tracks any injection drug use and frequency of injection drug use in the four weeks following release from jail.
Accidental Drug Overdose
Accidental drug overdose is defined as patient self-report of any event consistent with over-sedation or respiratory suppression following ingestion of alcohol, prescription, or illicit drugs.
Adverse Events and Serious Adverse Events
AEs and SAEs per standard definitions will be measured by self-report.

Full Information

First Posted
August 10, 2010
Last Updated
March 8, 2016
Sponsor
NYU Langone Health
Collaborators
Alkermes, Inc., New York City Department of Health and Mental Hygiene
search

1. Study Identification

Unique Protocol Identification Number
NCT01180647
Brief Title
Extended-Release Naltrexone for Opioid Relapse Prevention Following Release From Jail
Official Title
Extended-Release Naltrexone for Opioid Relapse Prevention Following Release From Jail
Study Type
Interventional

2. Study Status

Record Verification Date
March 2016
Overall Recruitment Status
Completed
Study Start Date
May 2010 (undefined)
Primary Completion Date
July 2013 (Actual)
Study Completion Date
July 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
NYU Langone Health
Collaborators
Alkermes, Inc., New York City Department of Health and Mental Hygiene

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This pilot study's primary aim is to compare rates of sustained opioid relapse, defined as self-reported opioid use >50% (>15 of 30) of days during the first 30 days following release from jail, among persons treated with XR-NTX pre-release vs. controls not receiving XR-NTX.
Detailed Description
This protocol randomizes persons soon-to-be-released from a large urban jail to treatment with extended-release naltrexone (XR-NTX), a full opioid antagonist that prevents the activity of heroin and other opioids. Investigators at NYUSOM and NYC DOHMH will recruit heroin dependent persons from NYC jails who are soon-to-be-released, not accessing opioid agonist pharmacotherapy, with lowered tolerance due to incarceration, and extremely likely to relapse and risk accidental overdose at release. All N=40 participants receive a two-session, individual psychosocial intervention, Motivational Interviewing. Half (n=20) will be randomized to pre-release treatment with XR-NTX. Immediately and one month following release, participants will be offered continued psychosocial and medication-assisted treatment (naltrexone, buprenorphine, or methadone) at Bellevue Hospital, including a second XR-NTX dose among XR-NTX arm participants. The primary outcome is relapse to sustained opioid use during the first 30 days post-release. We hypothesize an XR-NTX arm will report significantly lower rates of sustained opioid relapse following release.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Opiate Dependence
Keywords
Extended-release naltrexone, Prisoners, Opioid addiction prevention, Medication Treatment Alternatives, Prevention of Relapse to Opioid Addiction

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
48 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Extended-release naltrexone (XR-NTX)
Arm Type
Active Comparator
Arm Description
A single 380mg IM depot injection of XR-NTX in the week prior to release from jail. A second 380mg IM injection is offered to persons in the XR-NTX arm post-release and 4 weeks after the initial injection.
Arm Title
Motivational Enhancement Counseling Only
Arm Type
Placebo Comparator
Arm Description
The randomized control arm receives no medication treatment and is offered brief, two-session Motivational Enhancement counseling prior to release from jail.
Intervention Type
Drug
Intervention Name(s)
Extended-Release Naltrexone
Other Intervention Name(s)
Vivitrol
Intervention Description
380mg IM XR-NTX injection one week prior to release from jail; a second XR-NTX 380mg IM injection is offered 4 weeks later (monthly).
Intervention Type
Behavioral
Intervention Name(s)
Motivational Enhancement Counseling
Intervention Description
The randomized control arm receives no medication treatment and is offered brief, two-session Motivational Enhancement counseling prior to release from jail.
Primary Outcome Measure Information:
Title
Post-Release Opioid Relapse
Description
Post-release opioid relapse at week 4, measured by self-report (Time Line Follow Back) and urine toxicologies, and defined as ≥10 of 28 days of self-reported opioid misuse following jail release or two or three positive of the three urine samples during weeks 2, 3 and 4. A single positive or missing urine result counted as 7 opioid misuse days.
Time Frame
Four weeks post-release
Secondary Outcome Measure Information:
Title
Participation in Community Drug Treatment Post-release
Description
This secondary outcome tracks community drug treatment initiation four weeks post-release from jail. Measured by self-report community drug treatment initiation at week 4 study visit.
Time Frame
Four weeks post-release
Title
Any Opioid Use Post-release
Description
Counts of any opioid use, defined as self-reported ≥ 1 day of heroin or other opioid use as measured by the Timeline Follow-Back assessment during the first 4 weeks post-release.
Time Frame
Four weeks post-release
Title
Injection Drug Use Post-release
Description
This secondary outcome tracks any injection drug use and frequency of injection drug use in the four weeks following release from jail.
Time Frame
Four weeks post-release
Title
Accidental Drug Overdose
Description
Accidental drug overdose is defined as patient self-report of any event consistent with over-sedation or respiratory suppression following ingestion of alcohol, prescription, or illicit drugs.
Time Frame
Four weeks post-release
Title
Adverse Events and Serious Adverse Events
Description
AEs and SAEs per standard definitions will be measured by self-report.
Time Frame
Eight weeks post-release

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adults incarcerated in NYC jails with known release date DSM-IV criteria for current opioid dependence No current agonist (methadone, buprenorphine) treatment Currently opioid free by history ('detoxed') and with a negative urine for all opioids General good health as determined by complete medical interview and physical examination Age 18-60 years. Exclusion Criteria: History of liver failure, cirrhosis, or recent liver function test levels greater than three times normal Pregnancy, lactation, or planning conception Active medical illness that might make participation hazardous Untreated psychiatric disorder History of allergic reaction to naltrexone, PLG (polylactide co-glycolide), carboxymethylcellulose, or any other components of the diluent. Current chronic pain condition treated with opioids.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joshua D Lee, MD MSc
Organizational Affiliation
NYU School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
New York University School of Medicine
City
New York
State/Province
New York
ZIP/Postal Code
10016
Country
United States
Facility Name
New York City Department of Correction
City
New York
State/Province
New York
ZIP/Postal Code
11370
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
25703440
Citation
Lee JD, McDonald R, Grossman E, McNeely J, Laska E, Rotrosen J, Gourevitch MN. Opioid treatment at release from jail using extended-release naltrexone: a pilot proof-of-concept randomized effectiveness trial. Addiction. 2015 Jun;110(6):1008-14. doi: 10.1111/add.12894. Epub 2015 Apr 5.
Results Reference
derived

Learn more about this trial

Extended-Release Naltrexone for Opioid Relapse Prevention Following Release From Jail

We'll reach out to this number within 24 hrs