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Pre-operative or post-operative misoprostol in ceasrean delivery:Dose it differ?

Phase 4
Conditions
Finished
Registration Number
JPRN-UMIN000025363
Lead Sponsor
Tanta University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
Female
Target Recruitment
180
Inclusion Criteria

Not provided

Exclusion Criteria

conditions prolonging surgical time or causing atony as: general anesthesia , antepartum hemorrahge coagulation disorders Previous 2 or more cesarean sections previous rupture uterus muliple pregnancies, polyhydramios or macrosomia

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
amount of blood loss intraoperative and postoperative
Secondary Outcome Measures
NameTimeMethod
Drop in hematocrite level 24 hours after cesarean section and any drug related complications
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