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The effect of misoprostrol in reduction of postpartum hemorrhage

Phase 2
Conditions
reduction of postpartum haemorrhage.
Other immediate postpartum haemorrhage
Registration Number
IRCT138812223548N1
Lead Sponsor
Qazvin University Of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
300
Inclusion Criteria

pregnant women with singleton pregnancy, cephalic, spontaneous and induced delivery, term pregnancy. Exclusion criteria: instrumental delivery, TL during 24h after delivery, past history of abruption placenta, history of asthma, coagulopathy, history of postpartum hemorrhage, history of C/S.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Reduction of postpartum hemorrhage. Timepoint: in admission at labour and 24h after delivery. Method of measurement: blood sampling and CBC.
Secondary Outcome Measures
NameTimeMethod
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