Effect of prophylactic intravenous tranexamic acid on blood loss after cesarean delivery

Phase 1

• Conditions: postpartum blood loss.

• Registration Number: IRCT20091010002558N7
• Lead Sponsor: Ghoum University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 5 January 2021

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 44

Inclusion Criteria

Inclusion criteria included age 18-35 years, single pregnancy, cesarean delivery, blood pressure less than 140 over 90, no history of thromboembolism and coagulation disease, no uterine myoma, no IUFD fetus, no decolonization and no history or Active heart, liver and kidney diseases

Exclusion Criteria

During cesarean section, if placental adhesions such as placenta, increta and percorta are observed, individuals will be excluded.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Blood loss after cesarean. Timepoint: The lost blood will be controlled in two times: A: The time of placenta departure until the end of cesarean section B: From the end of cesarean section to 2 hours after delivery. Method of measurement: In practice, the volume of blood in the suction and the weight of the gases and blood-stained tampons will be used to check for postpartum hemorrhage. A digital scale (with an error rate of 10 grams) will be used to weigh gases and guns. To collect the blood lost after the cesarean section, immediately after the end of the cesarean section, a disposable plastic cover with a certain weight is spread under the cesarean section woman and she will be weighed 2 hours after the cesarean section.;Hemoglobin and hematocrit levels. Timepoint: Hemoglobin and hematocrit levels will be monitored before and 12-24 hours after delivery. Method of measurement: hemoglobin and hematocrit are measured by blood test.