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Clinical Trial Summary

In this study, our aim is to investigate the role tranexamic acid in modulating inflammation in patients with sepsis.


Clinical Trial Description

A written informed consent will be taken from the patients or their relatives.Patients will be assigned randomly to two groups (40 subjects each) with qSOFA ≥2. In (Group T) administer 1 gram of tranexamic acid (TXA) in 100 ml of 0.9% normal saline, intravenous over 10 minutes as soon as possible but no later than three hours after diagnosis, infuse a second gram of tranexamic acid (TXA) IV over 8 hours in 0.9% normal saline for the first 3 days. In (Group C) administer the same volume (100 ml normal saline)and same duration (first three days)for controlled patients. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04910464
Study type Interventional
Source Assiut University
Contact Omar Soliman
Phone 01101266040
Email omarmakram347@yahoo.com
Status Recruiting
Phase Phase 3
Start date June 5, 2021
Completion date June 30, 2024

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