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Study identifier: NCT06736860 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Tranexamic Acid in Patients With Traumatic Bleeding Based on Dynamic Monitoring of Thromboelastography

Condition: Trauma Coagulopathy  ·  Sponsor: Nanfang Hospital, Southern Medical University

PhasePhase 4
Planned participants580
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

Trauma is an important global public health problem and is the leading cause of death in people under 40 years old. Studies have shown that early prehospital administration of TXA 1 g intravenously followed by a continuous infusion of 1 g tranexamic acid (TXA) over 8 hours ( 1+1 regimen) is effective in reducing mortality in trauma patients, but there is a residual risk of death. This clinical study utilized real-time dynamic monitoring of coagulation fibrinolytic status in trauma patients using thromboelastography (TEG) to assess the need for a second or even multiple administrations of TXA (1+X regimen) in addition to the administration of 1 g of TXA intravenously and to compare the two mortality rates, thus guiding the early and precise use of TXA in trauma patients to potentially reduce mortality in trauma patients while decreasing thromboembolic risk. The present study is an optimization and addition to the TXA 1+1 regimen. Currently, no relevant studies have been reported. This study has important clinical significance for standardizing the early and precise use of TXA in trauma patients and improving the effectiveness and safety of TXA.

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

Talk to the study team

Xu Li, doctor  ·  +86 18680248866  ·  mylx99@smu.edu.cn

Always discuss trial participation with your own doctor first.

Locations (1)

Nanfang Hospital, Southern Medical UniversityGuangzhou, Guangdong, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06736860