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Role of oxytocin versus carbetocin in prevention of post partum haemorrhage in cesarean section

Role of oxytocin verses carbetocin in prevention of postpartum haemorrhage in cesarean section a randomised control trial. - Nil

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/10/059211
Enrollment
42
Registered
2023-10-27
Start date
Unknown
Completion date
Unknown
Last updated
2023-11-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O720- Third-stage hemorrhage

Interventions

Intervention1: Carbetocin: The study medication carbetocin 100 mcg will be diluted with 8 ml of normal saline and will be administered intravenously slowly over 2 -3 minutes after the birth of the b

Sponsors

Rajendra Institute of Medical Sciences Ranchi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.women with singleton pregnancy undergoing elective or emergency cesarean section with greater than or equal to 37 weeks of gestation . 2. Not hypersensitive to oxytocin or carbetocin

Exclusion criteria

Exclusion criteria: 1.women with multiple gestation ,morbidly adherent placenta 2. women undergoing cesarean section with general anaesthesia 3.thromboembolic disorder , coagulation defect

Design outcomes

Primary

MeasureTime frame
To find out the effectiveness of caebetocin versus oxytocin in prevention of postpartum haemorrhage in patients undergoing cesarean sectionTimepoint: Patient undergoing cesarean sections will be monitored for postpartum haemorrhage till 24 hours after the birth of baby .

Secondary

MeasureTime frame
1.To asses the need for other uterotonics drugs 2.To assess the need for blood transfusion in post partum haemorrhage. Timepoint: during cesarean section and within 24 hours of delivery.

Countries

India

Contacts

Public ContactDr shiwani kumari

Rajendra institute of medical sciences ranchi

myinbox.pooja@gmail.com7250754600

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026