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Sublingual Misoprostol to Reduce Blood Loss in Cesarean Delivery

Not Applicable
Conditions
Cesarean Section.
Single delivery by cesarean section
Registration Number
IRCT2016041125648N3
Lead Sponsor
Vice Chancellor for Research of Mashhad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
90
Inclusion Criteria

Inclusion criteria are: any of post partum hemorrhage risk factors in term pregnancies like uterine over distention (macrosomia or multiple pregnancies); arrested descent labor; prolonged induction.
Exclusion criteria are: coagulopathies; anemia; adhesion bands,; organ damage during surgery (intestine; colon; Bladder; etc); allergy for prostaglandins, abnormal placenta; need for extended surgery incision and underlying diseases (diabetes mellitus; hypertension; ischemic heart disease; etc).

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Serum Hemoglobin. Timepoint: Before/ after surgery. Method of measurement: Laboratory.;Need for additional uterotonic usage. Timepoint: During surgery. Method of measurement: Clinical.
Secondary Outcome Measures
NameTimeMethod
Hospital stay duration. Timepoint: N/A. Method of measurement: Duration between admission and discharge.
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