Bedside clotting study (Thromboelastography) for critical decision making in patients requiring massive blood transfusion at trauma centre.
Not Applicable
- Conditions
- Health Condition 1: R00-R99- Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified
- Registration Number
- CTRI/2022/04/042334
- Lead Sponsor
- ICMR
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
The study will include patients who meet the criteria for MTP activation and present within 8 hours of injury/trauma.
Exclusion Criteria
1.Patients in cardiac arrest
2.Patients referred from other hospital and have received blood products.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method