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Study identifier: NCT06699901 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Antibiotic Concentrations After MassivE Transfusion Study

Condition: Adverse Effects in the Therapeutic Use of Other and Unspecified Agents Affecting Blood Constituents  ·  Sponsor: Brooke Army Medical Center

PhaseN/A
Planned participants417
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Combat and civilian trauma frequently result in open wounds that are at risk for infection. Data from the Department of Defense Trauma Registry demonstrate that 74% of combat trauma casualties have an open wound. The Committee on Tactical Combat Casualty Care, the Prolonged Field Care Working Group, and the Joint Trauma System clinical practice guidelines recommend antibiotic prophylaxis for open wounds after trauma. The civilian setting has similar risks of open wound infection after trauma. In parallel, current practice guidelines recommend the aggressive use of balanced blood products during resuscitation. It remains unclear how the replacement of blood after hemorrhage through transfusion may affect antibiotic concentrations. Data is necessary to better understand this relationship to enhance wound prophylaxis antibiotic dosing, particularly in severely wounded casualties who receive blood products during massive transfusions. It remains unclear how these resuscitation methods may alter pharmacokinetics. The investigators hypothesize that drug concentrations decrease in direct relation to the amount of blood transfused during low-volume, massive, and supermassive transfusion after trauma compared to patients who receive no blood products. The investigators seek to understand the relationship between drug concentrations and blood product administration using a non-compartmentalized model in the setting of hemorrhage. Specifically, they will (1) obtain drug concentrations a…

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

Talk to the study team

Steven G Schauer, DO  ·  2109160808  ·  steven.g.schauer.mil@army.mil

Jessica Mendez, MS  ·  jessica.mendez32.ctr@health.mil

Always discuss trial participation with your own doctor first.

Locations (2)

University of Colorado HospitalAurora, Colorado, United StatesRecruiting
Brooke Army Medical CenterFort Sam Houston, Texas, United StatesNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT06699901