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Carbetocin versus Oxytocin for prevention of postpartum hemorrhage at cesarean sectio

Phase 3
Conditions
postpartum hemorrhage.
Postpartum care and examination
Registration Number
IRCT2015050919644N1
Lead Sponsor
Vice Chancellor for research, Zahedan University of Medical Science
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
90
Inclusion Criteria

Pregnant women with single pregnancy one previous cesarean section or primary cesarean and candidate for cesarean delivery & application of spinal anesthesia.
5-Exclusion criteria: Other reason of PPH except atonia; Presence of preeclampsia; hypotension; heart disease and asthma; Presence of risk factor of PPH such as uterine fibroid? previous myomectomy? placenta previa? past history of PPH? chorioamnionitis; fetal macrosomia and fetal malformations associated with polyhydramnios

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Hemoglobin level. Timepoint: Before and 6 and 12hours after cesarean delivery. Method of measurement: Hemoglobine assessment.
Secondary Outcome Measures
NameTimeMethod
terine tone. Timepoint: 2 and 12 and 24 hours after cesarean delivery. Method of measurement: Assessment of uterine tone.;Need to adminestration of utertonic drug. Timepoint: During 24 hours after cesarean delivery. Method of measurement: Dosage and amount of drug.;Adverse effects. Timepoint: During 24 hours after cesarean delivery. Method of measurement: Observation of adverse effects.
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