Clinical randomization of an Antifibrinolytic agent in Significant Haemorrhage
Not Applicable
- Conditions
- Haemorrhage following trauma
- Registration Number
- SLCTR/2007/008
- Lead Sponsor
- ondon School of Hygiene and Tropical Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow up complete
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
All patients whose age is 16 yrs old or above with significant haemorrhage following trauma.( systolic blood pressure 90 mm hg and / or heart rate is more than 110/ min.) within 8 hours of injury
Exclusion Criteria
Patient who requires tranexamic acid as a treatment or its use is contraindicated
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Death in hospital within 4 weeks of injury [Within 4 weeks of injury]<br>
- Secondary Outcome Measures
Name Time Method Receipt of a blood products transfusion, the number of units of blood products transfused, surgical intervention & the occurrence of thrombo- embolic episodes []<br>