๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-06-26

A Study to Compare the Efficacy and Safety of TachoSil and Surgicel Original as an Adjunct to Control Mild to Moderate Soft Tissue Bleeding During Surgery (NCT06664775)

An Open Label, Prospective, Randomized, Parallel Groups, Multicenter Study to Compare the Efficacy and Safety of TachoSilยฎ Versus Surgicelโ„ข Original (Oxidized Regenerated Cellulose) as an Adjunct to Control Mild to Moderate Soft Tissue Bleeding During Surgery.

๐ŸŸข Recruiting Phase3 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: Corza Medical GmbH

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

The purpose of this clinical study is to assess the efficacy and safety of TachoSil compared to the widely known and used for \> 60 years local hemostatic product Surgicel Original as an adjunct to control mild to moderate soft tissue bleeding during surgery.

Who can join: Review the eligibility criteria below.

Location: Torrance Memorial โ€” Torrance, California

Age range: 1 Month

๐Ÿงช Interventions in This Study

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 (9 Sites)

  • Torrance Memorial โ€” Torrance, California
  • St. Anthony Hospital โ€” Lakewood, Colorado
  • Georgetown University โ€” Washington D.C., District of Columbia
  • University Of Chicago โ€” Chicago, Illinois
  • Indiana University โ€” Indianapolis, Indiana
  • University of Louisville โ€” Louisville, Kentucky
  • Washington University โ€” St Louis, Missouri
  • Atrium Health Carolinas Medical Center โ€” Charlotte, North Carolina
  • The Ohio State University Medical Center โ€” Columbus, Ohio

๐Ÿ“ž Contact the Study Coordinator

Phone: (416) 578-9058

Email: Jeff.wilson@corza.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.

Explore by condition: All Hemorrhage clinical trials

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†—