Carbetocin vs Misoprostol for Postpartum Hemorrhage Prevention

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorWestern Galilee Hospital-Nahariya

About this trial

Postpartum hemorrhage (PPH) is a leading cause of maternal morbidity and mortality worldwide, particularly among women with known risk factors. Uterotonic agents are routinely administered after vaginal delivery to prevent excessive bleeding. Carbetocin, a long-acting oxytocin analogue, and misoprostol are both used for this purpose, but comparative data in high-risk vaginal deliveries remain limited.

This prospective randomized study aims to compare the effectiveness and safety of intravenous carbetocin versus rectal misoprostol for the prevention of postpartum hemorrhage in women with risk factors undergoing vaginal delivery at Galilee Medical Center. The primary outcome is the incidence of postpartum hemorrhage. Secondary outcomes include the need for additional uterotonic agents or surgical interventions, changes in hemoglobin levels, blood transfusion requirements, and maternal adverse effects.

Eligibility criteria

Qualifiers

Women aged 18 years or older

Singleton pregnancy

Gestational age 37-42 weeks

Cephalic presentation

Disqualifiers

Multiple gestation

Known major fetal anomalies

Intrauterine fetal demise (IUFD)

Contraindication to vaginal delivery

Trial design

Treatments tested in this trial

  • Carbetocin 100 Microgram/mL Solution for Injection
  • Misoprostol

Treatment groups

146 Participants
are divided into 2 treatment groups

Locations

This trial has no locations