Comparison of the effects of misoprostol and oxytocine on postpartum Hemorrhage
Phase 2
Completed
- Conditions
- Postpartum hemorrhage.Other immediate postpartum haemorrhage072.1
- Registration Number
- IRCT20100429003833N2
- Lead Sponsor
- Vice chancellor for Research,Tabriz University Of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 237
Inclusion Criteria
singleton pregnant women
elective cesarean delivery
Maximum history of once cesarean section
Exclusion Criteria
Preeclampsia
Cardiovascular diseases
Uterine myoma
A history of excessive bleeding after delivery.
Underlying disease, such as coagulopathy
Abnormal placental implantation (Placenta peria or Ecrta)
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Bleeding volume during cesarean section. Timepoint: After the placenta is removed until the uterus is repaired. Method of measurement: Number of gases and lumps of wet gases and volume of blood in suction.;Bleeding volume during the first 24 hours of cesarean section. Timepoint: Hemoglobin and hematocrit are measured 24 hours after surgery and compared with preoperative values. Method of measurement: blood test.;Duration of surgery. Timepoint: From the start of surgery to complete repair of the uterus. Method of measurement: Record start and end times.
- Secondary Outcome Measures
Name Time Method Drug side effects. Timepoint: From the time of hospitalization to the patient's discharge. Method of measurement: Control vital signs.