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Comparative Efficacy of Carbetocin and Oxytocin in Parturients at Risk of Atonic Postpartum Hemorrhage Undergoing Elective Cesarean Delivery

Not Applicable
Recruiting
Conditions
Post Partum Hemorrhage
Registration Number
NCT06333340
Lead Sponsor
Samuel Lunenfeld Research Institute, Mount Sinai Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
Not specified
Inclusion Criteria

Inclusion criteria - Any one or more of the risk factors for uterine atony:<br><br> - Overdistended uterus due to:<br><br> - Polyhydramnios (amniotic fluid index >24 cm)<br><br> - Fetal macrosomia reported on prenatal ultrasound >90th centile or > 4000 gm<br><br> - Multiple gestation<br><br> - History of uterine atony/PPH (documented with blood loss of >1000 ml, blood<br> transfusion, use surgical methods such as Bakri balloon, B-Lynch sutures, uterine<br> artery ligation or embolization)<br><br> - Obesity with body mass index (BMI) >40 kg/m2<br><br> - Diabetes mellitus on treatment<br><br> - Preeclampsia on treatment<br><br> - Placenta previa<br><br>Exclusion criteria:<br><br> - Valvular heart disease, arrhythmias, or heart failure<br><br> - Placenta accreta spectrum<br><br> - Bleeding disorder<br><br> - Anemia (<100 g/dl)<br><br> - Allergy or sensitivity to oxytocin or carbetocin

Exclusion Criteria

Not provided

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Proportion of parturients requiring additional uterotonic agents intraoperatively
Secondary Outcome Measures
NameTimeMethod
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