Clinical Trial

Blood Storage Related Mortality and Adverse Effects in Trauma Patients

Completed
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Summary
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
Protocol Amendment History 2 changes
critical Trial completed 2026-08-08
notable Enrollment reduced: 300 -> 101 participants 2026-08-08
Trial Details
NCT Number NCT07341139
Lead Sponsor Kocaeli City Hospital
Conditions Transfusion Adverse Reaction, Major Trauma, Blood Product Transfusion for All Conditions
Enrollment 101 participants
Start Date 2026-01-17
Primary Completion 2026-06-01 (estimated)
Study Completion 2026-06-01 (estimated)
Updated on ClinicalTrials.gov 2026-08-07