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Addition of 400 microgram misoprotol to routine management of third stage of labour in women at risk for bleeding after delivery.

Not Applicable
Recruiting
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
Inclusion Criteria

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%)

Exclusion Criteria

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
NameTimeMethod
Blood loss after delivery and incidence of Post partum HaemorrhageTimepoint: From delivery of the newborn to 1 hour after delivery
Secondary Outcome Measures
NameTimeMethod
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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