Comparison between misoprostol pushed rectally and given below tongue before cesarean section to control blood loss during and after the surgery.
Phase 3
- Conditions
- Health Condition 1: O721- Other immediate postpartum hemorrhageHealth Condition 2: O720- Third-stage hemorrhage
- Registration Number
- CTRI/2020/11/029043
- Lead Sponsor
- IPGMER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Term pregnancy, singleton pregnancy, scheduled for elective lower segment caesarean section under spinal anaesthesia.
Exclusion Criteria
Hb% < 10 gm%, multifetal gestation, antepartum haemorrhage, polyhydramnios, two or more previous caesarean section, hypertension in pregnancy, history of heart, liver and renal disorder, active thromboembolic disease or previous history of thromboembolism, hypersensitivity to prostaglandins.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Blood loss within 2hours of birth: The suction bottle is changed following delivery of baby and blood loss is measured from the amount of blood collected in suction bottle plus weight of wet mops and drapings- weight of dry mops and drapings (assuming density 1gm /cc)plus blood loss every 15 minutes within 2hours after delivery from the weight of wet sanitary pads - weight of dry sanitary pads (assuming density 1gm /cc) <br/ ><br>Timepoint: 2 hours
- Secondary Outcome Measures
Name Time Method 1.Blood loss within 24hrs of birth at every moment the women discard sanitary pads (weight of wet sanitary pad minus weight of dry sanitary pad),2. Hemoglobulin and hematocrit before delivery and 24 hours after delivery, 3.Maternal death, maternal critical care unit admission, major surgical or invasive procedure, blood transfusion.Timepoint: 24 hours