Addition of 400 microgram misoprotol to routine management of third stage of labour in women at risk for bleeding after delivery.
- Conditions
- Health Condition 1: null- Pregant women with known High risk factors for post partum hemorrhage.
- Registration Number
- CTRI/2014/03/004491
- Lead Sponsor
- RS MEDICAL COLLEGE KOLKATA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 200
Women with one or more of the high risk factors as
multiple pregnancy
•polyhydramnios
•prolonged labour
•labor augmented by oxytocin.
•H/O PPH in previous pregnancy.
•Post caesarean section (for vaginal delivery)
•Obese patient (BMJ >30)
•Grand multipara
•APH
•Severe preeclampsia/eclampsia.
•Anaemia(hb <10gm%)
Any contraindications for the use of misoprostol and oxytocin such as known hypersensitivity, asthma, epilepsy etc.
Cardiovascular, hepatic, haematological disorders.
Temperature >38ï?°C
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Blood loss after delivery and incidence of Post partum HaemorrhageTimepoint: From delivery of the newborn to 1 hour after delivery
- Secondary Outcome Measures
Name Time Method 1.Post parum drop of Haemoglobin concentration <br/ ><br>2. need for additional oxytocic and blood transfusion <br/ ><br>3. complications and side effectsTimepoint: 1. 24 hours after delivery <br/ ><br>2. 24 hours after delivery <br/ ><br>3. 24 hours after delivery
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