postpartum blood loss.
Conditions
Interventions
Intervention 1: Intervention group: Women in the study group, received one gram intravenous TA, 10 min before skin incision in 200 mL normal saline over 10 min. In this study, TA was supplied in 2 × 5
Sponsors
Ghoum University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 35 Years
Inclusion criteria
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
Exclusion criteria: During cesarean section, if placental adhesions such as placenta, increta and percorta are observed, individuals will be excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactEsmat Jafarbegloo
Ghoum University of Medical Sciences
Outcome results
None listed