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Comparing injection carbetocin and oxytocin in prevention of bleeding during cesarean delivery

Carbetocin and oxytocin in elective cesarean delivery in patients with high risk of postpartum hemorrhage under spinal anesthesia a comparative double blind randomized control study - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/04/065748
Enrollment
120
Registered
2024-04-16
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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: injection of uterotonic agents: intravenous injection carbetocin 100mcg bolus over 1 minute and oxytocin 20IU in 1000ml Normal saline(0.9%) at 150ml/hr given after delivery of anterior

Sponsors

Tezpur medical college and hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Parturients of the ASA grade 1 and 2 with gestation of 37 weeks or more, who had an elective cesarean delivery under spinal anesthesia with risk factors of postpartum haemorrhage such as multiple pregnancy,two or more previous cesarean section,presence of uterine fibroids,previous myomectomy,past history of postpartum haemprrhage,prolonged labor,fetal macrosomia,BMI 35 and more and fetal malformations with polyhydramnios

Exclusion criteria

Exclusion criteria: ASA garde 2, allergy to study drugs,patients contraindicated for spinal anesthesia,Declined to participate,premature rupture of memebrane,pregnancy induced hypertension,antepartum haemorrhage,patients in active labor,inadequate block after apinal anaesthesia,history of epilepsy,diabetes mellitus,ischemic heart disease,cerebrovascular disease,hepatic and renal disease

Design outcomes

Primary

MeasureTime frame
To assess the efficacy of Oxytocin and carbetocin in terms of adequate uterine contractility and prevention of intraoperative blood lossTimepoint: To assess the efficacy of Oxytocin and carbetocin in terms of adequate uterine contractility and prevention of intraoperative blood loss in first 24 hrs of delivery

Secondary

MeasureTime frame
compare the heamodynamic effects of carbetocin and oxytocin(HR,MAP,ECG) to asses the need for additional uterotonics in cesarean section at high risk of PPH adverse effects of Oxytocin and carbetocinTimepoint: heamodynamic stability in each group for 24 hrs

Countries

India

Contacts

Public ContactDilip kumar saloi

Tezpur medical college and hospital

dilipkumarsaloi@gmail.com9101291318

Outcome results

None listed

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