Buprenorphine Implementation at Syringe Service Programs to Reduce Overdoses
Montefiore Medical Center · with National Institute on Drug Abuse (NIDA), New York University · NCT07631598
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 512
- US sites recruiting
- 8
- Study start
- August 17, 2026
- Record last updated
- October 1, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
This study is testing whether offering buprenorphine treatment directly at syringe service programs (SSPs) helps more people start and stay in treatment for opioid use disorder (OUD) than referring them to community buprenorphine treatment providers. Buprenorphine is a medication that helps reduce opioid cravings and withdrawal symptoms.
The study compares two ways of connecting people to treatment:
Referral to a community treatment provider (usual care before the new program begins).
Onsite, low-threshold buprenorphine treatment at the SSP, which allows participants to start medication quickly and without having to establish care at another provider.
Participants will be adults who have opioid use disorder and are SSP clients. Each SSP will begin offering the new onsite buprenorphine program at different times during the study. Researchers will collect information before and after the new program begins to see how it affects treatment engagement and health outcomes.
The study will also examine how easy or difficult it is for SSPs to start and run the new program, how acceptable it is to staff and participants, and whether it is cost-effective.
The overall goal is to find better ways to expand access to life-saving opioid treatment in community-based settings.
Being studied: Standard of Care Referral; Low Threshold Buprenorphine
Conditions: Opioid Use Disorder; Opioid Use Disorder, Severe; Opioid Use Disorder, Moderate
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- ≥ 18 years old;
- Meet DSM-5 criteria for moderate or severe OUD;
- Interest in receiving buprenorphine treatment;
- Speaks English or Spanish;
- Currently an SSP client at the time of enrollment;
- Ability to provide informed consent.
Exclusion Criteria
- Current use of prescribed opioid agonist treatment, as assessed by self-report, at the time of enrollment;
- Unstable mental health or medical condition that requires an immediate clinical evaluation or higher level of care;
- Allergy to buprenorphine;
- Currently detained in jail, prison, residential substance use treatment facility, or other overnight facility as required by court of law. or have pending legal action that could prevent participation on study activities.
Recruiting US locations
Community Health Project Los Angeles (CHPLA)
Los Angeles, CA 90029
Site contact: Site PI · 323-380-5469 · info@chpla.org
HIPS
Washington D.C., DC 20002
Site contact: Phyllis Bijole · 202-834-3289 · phyllis@hips.org
CARPBR/Be Safe Syringe Program
Baton Rouge, LA 70806
Site contact: Site PI · 225-775-7988 · gjvar.carpbr@gmail.com
Harm Reduction Sisters
Duluth, MN 55805
Site contact: Jack Research Coordinator · 218-206-6482 · jack@harmreductionsisters.org
Alianza of New Mexico
Roswell, NM 88203
Site contact: Ryan Nix Site PI · 575-623-1995 · ryan.nix@alianzanm.org
HIV Alliance
Grants Pass, OR 97526
Site contact: Harmony Beckett · 541-342-5088 · hbeckett@allianceor.org
Challenges, Inc/Prisma Health
Greenville, SC 29605
Site contact: Liam Diaz, MPH · 864-915-2528 · Liam.Diaz@prismahealth.org
Vivent Health
Milwaukee, WI 53212
Site contact: Site PI · 800-359-9272 · ctgov.research@viventhealth.org
Study contacts (from the official record)
- Megan M Ghiroli · 12036068136 · mghiroli@montefiore.org
- Aaron D Fox, MD, MS · adfox@montefiore.org
Similar studies in California
All healthy volunteers studies in California →- RecruitingHealthy volunteersPhase 1Overnight stay mentioned
A Study to Investigate the Relative Bioavailability and Safety of Different Oral Formulations of Elecoglipron in Healthy Participants
AstraZeneca
- Location
- Glendale, CA + 1 other US site
- Eligibility basics
- Ages 18–55
- RecruitingHealthy volunteersPhase 1Overnight stay mentioned
A Phase I Study to Investigate the Pharmacokinetics and Safety of Capivasertib in Participants With Moderate Hepatic Impairment
AstraZeneca
- Location
- Rialto, CA + 1 other US site
- Eligibility basics
- Ages 18–80
- RecruitingHealthy volunteersPhase 1Overnight stay mentioned
A Study to Learn How the Body Processes the Study Medicine PF-07328948 in People With Reduced Kidney Function
Pfizer
- Location
- Lake Forest, CA + 3 other US sites
- Eligibility basics
- Ages 18–80
- RecruitingHealthy volunteersPhase 1Overnight stay mentioned
Phase 1 Study of SBS-147 in Healthy Adults
Sparian Biosciences, Inc
- Location
- Cypress, CA
- Eligibility basics
- Ages 18–55