A study to measure the efficacy of tranexamic acid to reduce post partum haemorrhage volume
Not Applicable
Completed
- Conditions
- Post-partum haemorrhagePregnancy and Childbirth
- Registration Number
- ISRCTN09968140
- Lead Sponsor
- niversity Hospital Research Delegation of Lille (France)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 144
Inclusion Criteria
Patients were included in the study when PPH was more than 800 mL
Exclusion Criteria
1. Age < 18 years
2. Asence of informed consent
3. Caesarean section
4. Presence of known haemostatic abnormalities before pregnancy
5. History of previous thrombosis or epilepsy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The volume of blood loss between enrollment and 6 hours later
- Secondary Outcome Measures
Name Time Method