Comparative study of tranexamic acid
Phase 3
Recruiting
- Conditions
- Occurrence of postpartum hemorrhage.
- Registration Number
- IRCT20101130005280N44
- Lead Sponsor
- Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 214
Inclusion Criteria
For pregnant mothers between 37-40 weeks,
age between 20 to 40 years
Satisfaction to participate in the study
History of postpartum hemorrhage in previous pregnancy
Macrosomic more than 4 kg
Polyhydramnios
History of thromboembolic events
Lower limb varicose veins
aggregate more than 24 hours
Very fast labor and high parity
Chorioamnionitis and placental abruption
Exclusion Criteria
Multiple pregnancies
Placental abnormalities
Preeclampsia
Liver disorders Kidney, brain and ...
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The amount of bleeding. Timepoint: In the first 2 hours (each quarter) and 12 and 24 hours after delivery. Method of measurement: Measure the amount of blood lost.;The amount of hemoglobin drop in both groups. Timepoint: In the first 2 hours (each quarter) and 12 and 24 hours after delivery. Method of measurement: The amount of hemoglobin is checked before and after delivery.
- Secondary Outcome Measures
Name Time Method