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 Surgicelโข Original (Oxidized Regenerated Cellulose) as an Adjunct to Control Mild to Moderate Soft Tissue Bleeding During Surgery.
๐ฉบ 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
๐งช Interventions in This Study
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ 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
๐ 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.
๐ฐ 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.
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๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.