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The effect of misoprostol on the amount of bleeding in cesarean sectio

Phase 2
Conditions
Cesarean section.
Registration Number
IRCT20180107038254N1
Lead Sponsor
Zahedan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
120
Inclusion Criteria

All full-term pregnant women candidate for elective cesarean section

Exclusion Criteria

Placenta previa
Diabetes mellitus
Active labor
Using anti-coagulant drugs

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Hemoglobin level. Timepoint: Before and after cesarean section. Method of measurement: Measured by laboratory.;Amount of blood loss. Timepoint: During cesarean section. Method of measurement: By measuring the amount of blood in suction set and the number of bloody guazes.
Secondary Outcome Measures
NameTimeMethod
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