๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-01-09

A Study Comparing Oral Buprenorphine and Injectable Buprenorphine for the Treatment of Opioid Use Disorder (NCT04375033)

CSP #2014 - Comparative Effectiveness of Two Formulations of Buprenorphine for Treating Opioid Use Disorder in Veterans (VA-BRAVE)

๐ŸŸข Recruiting Phase4 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: VA Office of Research and Development

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

VA-BRAVE will determine whether a 28-day long-acting injectable sub-cutaneous formulation of buprenorphine at a target dose of 300mg is superior in retaining Veterans in opioid treatment and in sustaining opioid abstinence compared to the daily sublingual (under the tongue) buprenorphine formulation at a target dose of 4-32 mg (standard of care). This is an open-label, randomized, controlled trial including 952 Veterans with opioid use disorder (OUD) recruited over 7 years and followed actively for 52 weeks. There are a number of secondary objectives that will be studied as well and include: comorbid substance use, both non-fatal and fatal opioid overdose, HIV and Hepatitis B (HBV) and C (HCV) testing results and risk behaviors, incarceration, quality of life, psychiatric symptoms of depression and posttraumatic stress disorder, housing status, dental health and utilization, and cost-effectiveness.

Who can join: Review the eligibility criteria below.

Location: Tuscaloosa VA Medical Center, Tuscaloosa, AL โ€” Tuscaloosa, Alabama

Age range: 18 Years

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (25 Sites)

  • Tuscaloosa VA Medical Center, Tuscaloosa, AL โ€” Tuscaloosa, Alabama
  • Phoenix VA Health Care System, Phoenix, AZ โ€” Phoenix, Arizona
  • VA Long Beach Healthcare System, Long Beach, CA โ€” Long Beach, California
  • VA Palo Alto Health Care System, Palo Alto, CA โ€” Palo Alto, California
  • San Francisco VA Medical Center, San Francisco, CA โ€” San Francisco, California
  • CERC (VISN1, West Haven, CT) โ€” West Haven, Connecticut
  • VA Connecticut Healthcare System West Haven Campus, West Haven, CT โ€” West Haven, Connecticut
  • Wilmington VA Medical Center, Wilmington, DE โ€” Wilmington, Delaware
  • Bay Pines VA Healthcare System, Pay Pines, FL โ€” Bay Pines, Florida
  • North Florida/South Georgia Veterans Health System, Gainesville, FL โ€” Gainesville, Florida
  • VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA โ€” Boston, Massachusetts
  • Minneapolis VA Health Care System, Minneapolis, MN โ€” Minneapolis, Minnesota
  • Louis Stokes VA Medical Center, Cleveland, OH โ€” Cleveland, Ohio
  • Dayton VA Medical Center, Dayton, OH โ€” Dayton, Ohio
  • Philadelphia MultiService Center, Philadelphia, PA โ€” Philadelphia, Pennsylvania
  • VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PA โ€” Pittsburgh, Pennsylvania
  • Providence VA Medical Center, Providence, RI โ€” Providence, Rhode Island
  • VA North Texas Health Care System Dallas VA Medical Center, Dallas, TX โ€” Dallas, Texas
  • VA Salt Lake City Health Care System, Salt Lake City, UT โ€” Salt Lake City, Utah
  • White River Junction VA Medical Center, White River Junction, VT โ€” White River Junction, Vermont
  • Hampton VA Medical Center, Hampton, VA โ€” Hampton, Virginia
  • Salem VA Medical Center, Salem, VA โ€” Salem, Virginia
  • VA Puget Sound Health Care System Seattle Division, Seattle, WA โ€” Seattle, Washington
  • Huntington VA Medical Center, Huntington, WV โ€” Huntington, West Virginia
  • Clement J. Zablocki VA Medical Center, Milwaukee, WI โ€” Milwaukee, Wisconsin

๐Ÿ“ž Contact the Study Coordinator

Phone: (857) 364-2888

Email: avron.spiro@va.gov

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—