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Comparison the effect of intravenous Tranexamic Acid and sublingual Misoprostol and Oxytocin to reducing of post- cesarean hemorrhage

Phase 2
Completed
Conditions
Postpartum haemorrhage.
Postpartum haemorrhage
Registration Number
IRCT201708308611N6
Lead Sponsor
Vice-Chancellor for Research of Qazvin University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
150
Inclusion Criteria

Inclusion criteria are singleton pregnant women with 37- 40 weeks gestational ages, first gravida and maximum second gravida; previous cesarean section with lower segment incision. Exclusion criteria: preeclampsia; abnormal placenta; previous uterine rupture.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Blood pressure. Timepoint: Every 5 minutes during the section and every 30 minutes up to an hour after cesarean. Method of measurement: Blood pressure monitor.;Pluse rate. Timepoint: Every 5 minutes during the section and every 30 minutes up to an hour after cesarean. Method of measurement: Blood pressure monitor.;Volume od bleeding. Timepoint: After removing placenta. Method of measurement: Through suction, weight of cesarean section's set and consumed gases.
Secondary Outcome Measures
NameTimeMethod
ausea. Timepoint: One hour after cesarean section. Method of measurement: Ask the patient.;Hemoglobin. Timepoint: At the time of entering the patient's in the ward and 24 hours after cesarean section. Method of measurement: Blood sample.;Fever. Timepoint: One hour after cesarean section. Method of measurement: Thermometer.;Shivering. Timepoint: One hour after cesarean section. Method of measurement: Observation.
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