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NCT Number: NCT06306443

Buprenorphine for Individuals in Jail

This study is an open label randomized controlled trial of extended-release buprenorphine (BRIXADI, XR-B) vs. sublingual buprenorphine (SL-B) in a large metropolitan jail. An open-label design will randomly assign 240 adults with moderate-to-severe OUDs who are soon-to-be-released from jail to either XR-B (n=120) or SL-B (n=120) treatment in jail followed by 6-months of post-release buprenorphine treatment, a 7-month safety visit, and a final long-term follow-up at 12-months.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Baltimore Central Booking & Intake Center, Baltimore, Maryland, United States

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About this study

This study is an open label randomized controlled trial of extended-release buprenorphine (BRIXADI, XR-B) vs. sublingual buprenorphine (SL-B) in a large metropolitan jail. An open-label design will randomly assign 240 adults with moderate-to-severe OUDs who are soon-to-be-released from jail to either XR-B (n=120) or SL-B (n=120) treatment in jail followed by 6-months of post-release buprenorphine treatment, a 7-month safety visit, and a final long-term follow-up at 12-months.

Aim 1. Compare the effectiveness of XR-B vs. SL-B Aim 2. To calculate the cost to the state and/or jail/city health system of implementing XR-B and SL-B, and determine the relative value, including the costs associated with the interventions in the community, from a county and state-policymaker and societal perspective.

Aim 3. Explore barriers and facilitators to XR-B versus SL-B implementation in jail: (1) dose induction; (2) diversion and procedures for reducing diversion; (3) continuity of care after release or transfer to another facility; (4) staffing (both custody and medical) needs for daily versus XR-B buprenorphine dosing; and (5) patient preference for XR-B versus SL-B.

Primary Outcome. (a) illicit opioid use (i. urine toxicology; ii. self-reported days of opioid use using Timeline Followback; and iii. time to opioid relapse).

Secondary Outcomes. (b) retention in buprenorphine treatment (i. days receiving buprenorphine and ii. time to treatment dropout); (c) other illicit substance use (i. urine toxicology; ii. self-reported days of illicit substance use using Timeline Followback; (d) overdose events (non-fatal and fatal); (e) quality of life (i. physical health; ii. mental health); (f) HIV risk behaviors (i. sexual risk behavior; ii. needle use or sharing); and (g) criminal activity (i. crime days; ii. re-arrest; iii. technical violations; iv. re-incarceration).

Costs. (a) cost to the correctional system; (b) costs associated with community intervention

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Adult male or female inmates at participating jail who are eligible for release within 120 days (sentenced and/or pretrial [note: individuals who might be sentenced to state/federal prison will be excluded]); Those individuals who are pre-trial and/or sentenced who are completing their sentence in the community (probation, parole, home detention, electronic monitoring, drug or other treatment court [or equivalent]) will be eligible to participate;
  • History of opioid use disorder (meeting DSM-5 criteria of moderate or severe opioid use disorder at the time of incarceration; individuals not meeting the opioid-disorder criterion will be eligible if they were treated in an opioid agonist treatment program during the year before incarceration);
  • Suitability for XR-B and/or SL-B treatment as determined by medical evaluation;
  • Willingness to enroll in XR-B or SL-B treatment in jail and continue in the community;
  • Planning to live in Baltimore City or the Baltimore Region;

Exclusion criteria

  • Liver function test levels greater than 5 times normal (if we are unable to obtain labs, a determination by the study physician will be made to allow inclusion);
  • Active medical illness that may make participation hazardous (e.g., unstable diabetes, heart disease; moderate to severe renal impairment; adequately treated medical conditions are acceptable);
  • Conditions or medications that may predispose to QTc prolongation (personal or family history of long QT syndrome, hypokalemia, medications that prolong QTc interval, e.g., macrolide antibiotics, azole antifungal compounds, anti-arrythmics, antipsychotics and antidepressant);
  • Untreated psychiatric disorder that may make participation hazardous (e.g., untreated psychosis, bipolar disorder with mania; adequately treated psychiatric disorders and appropriate psychotropic medications will be allowed);
  • History of allergic reaction to buprenorphine;
  • Suicidal ideation (within the past 6 months);
  • Inability to pass a study enrollment quiz; and
  • Currently receiving non-buprenorphine MOUD in jail (methadone, naltrexone).

Treatment and study plan

extended-release buprenorphine (XR-B)

Drug

buprenorphine

Other names: sublingual buprenorphine (SL-B)

Primary outcomes

  1. urine toxicology

    Time frame: 12-months

    positive urine drug screen for opioids

  2. days of opioid use

    Time frame: 12-months

    Number of days since last assessment

  3. time to opioid relapse

    Time frame: 12-months

    days from release from jail to first relapse event

Secondary outcomes

  1. retention in buprenorphine treatment

    Time frame: 6-months

    days receiving buprenorphine

  2. urine toxicology for other illicit substance use

    Time frame: 12-months

    positive urine drug screen

  3. days of illicit substance use

    Time frame: 12-months

    number of days since last assessment

  4. overdose events

    Time frame: 12-months

    fatal and non-fatal overdose events

  5. PROMIS Patient-Reported Outcomes Measurement Information System - physical health

    Time frame: 12-months

    Global physical health score

  6. PROMIS Patient-Reported Outcomes Measurement Information System - mental health

    Time frame: 12-months

    Global mental health score

  7. HIV risk behaviors (Risk Assessment Battery, RAB) - sex risk score

    Time frame: 12-months

    sexual risk behavior; Scored 0-18 (higher risk)

  8. HIV risk behaviors (Risk Assessment Battery, RAB) needle use or sharing score

    Time frame: 12-months

    needle use or sharing; Scored 0-22 (higher risk)

  9. criminal activity

    Time frame: 12-months

    i. crime days; ii. re-arrest; iii. technical violations; iv. re-incarceration

Study contacts

Contact information is provided by the study sponsor or research team.

Michael Gordon, DPA

CONTACT

[email protected]

4108373977 ext. 251

Thomas R Blue, PhD

CONTACT

[email protected]

4108373977

Sponsors and collaborators

Lead sponsor

Friends Research Institute, Inc.

Other

Registry information

Official study title

A Comparative Effectiveness Trial of Sublingual Versus Extended-release Buprenorphine With Individuals Leaving a Carceral Setting

Important dates

Study start
2025
Primary completion
2029
Study completion
2029
First posted
Mar 12, 2024
Registry last updated
Jun 4, 2026

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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