Trauma Resuscitation With Low-Titer Group O Whole Blood or Products (NCT05638581)
๐ฉบ Plain-English Summary (8th-Grade Level)
The goal of this clinical trial is to compare the effectiveness of unseparated whole blood (referred to as Low-Titer Group O Whole Blood) and the separate components of whole blood (including red cells, plasma, platelets, and cryoprecipitate) in critically injured patients who require large-volume blood transfusions.
Who can join: Review the eligibility criteria below.
Location: University of Alabama at Birmingham, UAB Hospital โ Birmingham, Alabama
Age range: 15 Years
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 (13 Sites)
- University of Alabama at Birmingham, UAB Hospital โ Birmingham, Alabama
- Los Angeles County + University of Southern California (LAC + USC) Medical Center โ Los Angeles, California
- University Medical Center New Orleans LCMC Health โ New Orleans, Louisiana
- University of Maryland Medical Center โ Baltimore, Maryland
- Washington University School of Medicine โ St Louis, Missouri
- Atrium Health Wake Forest Baptist โ Winston-Salem, North Carolina
- University of Cincinnati Medical Center โ Cincinnati, Ohio
- Oregon Health and Sciences University Hospital โ Portland, Oregon
- Penn Presbyterian Medical Center โ Philadelphia, Pennsylvania
- University of Texas Health Science Center Houston โ Houston, Texas
- University of Texas Health San Antonio and University Health System โ San Antonio, Texas
- Harborview Medical Center โ Seattle, Washington
- Froedtert Hospital โ Milwaukee, Wisconsin
๐ Contact the Study Coordinator
Phone: (205) 934-5890
Email: swstephens@uabmc.edu
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.
More studies in Wounds and Injuries
- Use of a Compression Device for Ring Removal: A Prospective Trial โ Halifax, Nova Scotia
- Feasibility Study for Fibroblast Autologous Skin Grafts โ Baltimore, Maryland
- Acute Partial Thickness Burn Study Comparing Transforming Powder Dressing to Standard of Care Dressing โ Orange, California
- APPRAISE 2.0: Live Trial of the APPRAISE Trauma Decision Support System โ Boston, Massachusetts
- Food is Medicine Prospective Study โ Los Angeles, California
Explore by condition: All Wounds and Injuries clinical trials
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.