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A comparison of rectal and sublingual Misoprostol on Post -Partum haemorrhage during cesarean sectio

Phase 3
Conditions
bleeding during and after cesarean section.
Registration Number
IRCT20190204042614N1
Lead Sponsor
Yazd University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
80
Inclusion Criteria

Pregnant women who were candidates of Cesarean section

Exclusion Criteria

pregnancy induced hypertension
twin pregnancy
sensitivity to prostaglandin
fetal distress

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Hemoglobin before and after surgery. Timepoint: 6 hours after surgery. Method of measurement: Cell counter machine.;Hematocrit before and after surgery. Timepoint: 6 hours after surgery. Method of measurement: Cell counter machine.
Secondary Outcome Measures
NameTimeMethod
Blood pressure. Timepoint: Every 5 minutes during surgery, every 15 minutes in recovery. Method of measurement: Device monitoring.;Heart beat. Timepoint: Every 5 minutes during surgery, every 15 minutes in recovery. Method of measurement: Device monitoring.
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