๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-08-17

Radial vs. State-Of-The-Art Femoral Access for Bleeding and Access Site Complication Reduction in Cardiac Catheterization (REBIRTH) (NCT04077762)

Radial vs. State-Of-The-Art Femoral Access for Bleeding and Access SIte Complication Reduction in Cardiac Catheterization (REBIRTH)

๐ŸŸข Recruiting Observational / Diagnostic ๐Ÿฉบ Clinical Procedure Protocol Sponsor: Minneapolis Heart Institute Foundation

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

This is a phase IV, prospective, open label, randomized-controlled study that will compare radial access with state-of-the-art femoral access in patients without ST-segment elevation acute myocardial infarction undergoing cardiac catheterization. Subjects will be randomized 1:1 into 2 treatment groups: radial access and state-of-the-art femoral access. Randomization will be performed in blocks of 50 per site. Similarly, a second sub-randomization will be performed in the femoral access group into use of 18 vs 21 gauge needles, also in a 1:1 fashion.

Who can join: Review the eligibility criteria below.

Location: San Francisco VA Medical Center โ€” San Francisco, California

Age range: 18 Years

๐Ÿงช Interventions in This Study

  • Radial Access (PROCEDURE)
  • State-of-the-art femoral access with 18 gauge needle (PROCEDURE)
  • State-of-the-art femoral access with 21 gauge needle (PROCEDURE)

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 (6 Sites)

  • San Francisco VA Medical Center โ€” San Francisco, California
  • Mayo Clinic Florida โ€” Jacksonville, Florida
  • Joseph Maxwell Cleland Atlanta VA Medical Center โ€” Decatur, Georgia
  • Henry Ford Hospital โ€” Detroit, Michigan
  • Minneapolis Heart Institute Foundation โ€” Minneapolis, Minnesota
  • Oklahoma Heart Hospital โ€” Oklahoma City, Oklahoma

๐Ÿ“ž Contact the Study Coordinator

Phone: (612) 863-3852

Email: bavana.rangan@allina.com

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†—