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Study identifier: NCT07341139 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Blood Storage Related Mortality and Adverse Effects in Trauma Patients

Condition: Transfusion Adverse Reaction · Major Trauma · Blood Product Transfusion for All Conditions  ·  Sponsor: Kocaeli City Hospital

PhaseN/A
Planned participants300
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

The purpose of this retrospective study is to examine the following factors related to blood storage time in severely injured trauma patients who received large blood transfusions: 1. The effect of blood storage time on the patient's 28-day mortality rate. 2. The relationship between storage time and other health problems that the patient may develop (such as heart disease, vascular occlusion, respiratory failure, infection, and organ failure). For this purpose, patients aged 18-75 who were admitted directly from the scene of injury and received large transfusions at Jacksonville Shands Hospital between January 1, 2023, and October 1, 2025, will be included. Data will be obtained from hospital information systems and anesthesia records

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

Talk to the study team

ayten saracoglu, prof dr  ·  +1 (904) 5245932  ·  anesthesiayten@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

UF Health Jacksonville (Shands Hospital)Jacksonville, Florida, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07341139