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Study identifier: NCT05756426 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Consortium for Optimized Integration of Bio-Artificial Blood Components for Adaptive Resuscitation Therapy

Condition: Hemorrhage · Hemodynamic Instability  ·  Sponsor: University of Maryland, Baltimore

PhaseN/A
Planned participants250
Who can joinAll sexes, 18 Years to 88 Years
Healthy volunteersYes

About this study

There is need for a whole blood analog for use when banked blood is unavailable or undesirable. In civilian trauma, hemorrhage accounts for \~ 35% of pre-hospital deaths; moreover, \~ 20% of military casualties are in hemorrhagic shock on arrival to field hospitals and an additional 5% require urgent transfusion. A recent review concluded that hemorrhage accounted for \~ 90% of potentially survivable battlefield deaths - lives that could be saved with better hemorrhage control capabilities and improved, field-ready blood, blood components, or blood substitutes. While study of ideal composition for resuscitative fluids is ongoing, it is evident that for those in hemorrhagic shock, volume replenishment alone (without O2 carrying capacity) is insufficient. Alternatively, with massive blood loss or with ongoing bleeding from non-compressible injuries, resuscitation with an O2 carrier alone may be complicated by acquired coagulopathy (either dilutional or trauma-induced). Development of a balanced resuscitation fluid that treats both shock and coagulopathy (comprising a field-deployable O2 carrier with lyophilized humoral hemostatic components and platelets) is essential to allow on-scene treatment during the critical 'golden-hours' after injury. As such, the whole blood analog described herein could be this product, thus transforming care in both civilian and military settings.The scientific purpose of this study is to develop a combined whole blood substitute from individual a…

This description comes directly from the study's public registry record.

Talk to the study team

Stephen Rogers, PhD  ·  410-706-7094  ·  stephen.rogers@som.umaryland.edu

Tobi Rowden, RN  ·  410-706-7094  ·  trowden@som.umaryland.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of Maryland Baltimore (UMB)Baltimore, Maryland, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05756426