comparison of changes in blood pressure following supplementation of either of the two drugs named oxytocin and carbetocin in surgeries done in pregnant mothers following the delivery of the baby.

A prospective randomized study comparing the mean arterial pressure variations following administration of oxytocin and carbetocin in elective cesarean section under subarachnoid blockade - Nil

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/05/067030

Enrollment

Registered

2024-05-08

Start date

Unknown

Completion date

Unknown

Last updated

2024-05-27

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

Conditions

Health Condition 1: O80- Encounter for full-term uncomplicated delivery

Interventions

Intervention1: Oxytocin: Comparing the mean arterial pressure variations in elective LSCS Control Intervention1: Carbetocin: To intervene the changes in the blood pressure during caeserean surgeries

Eligibility

Inclusion criteria

Inclusion criteria: 1.Parturient acceptance 2.ASA status 2 and 3 3.Age between 20-30 yrs. 4.Parturient of term gestation undergoing elective lower segment cesarean section under spinal anesthesia

Exclusion criteria

Exclusion criteria: 1.Absolute contraindications for spinal anesthesia 2.Combined spinal epidural anesthesia 3.Short stature 40 4.Conditions associated with increased level of PPH risk (placenta previa, placentalabruption, multiple gestation)

Design outcomes

Primary

Measure	Time frame
The primary objective of this study is to compare the mean arterial blood pressure variation following administration of oxytocin and carbetocin in lower segment cesarean section.Timepoint: Baseline, 1,3,5,10 minutes and every 2nd minute following delivery of baby till 20 minutes	—

Secondary

Measure	Time frame
The secondary objective focusses on 1.Heart rate variations occurring between oxytocin and carbetocin 2.Requirement of vasopressor - phenylephrine 3.Clinical estimation of blood loss 4.Side effects and complications of oxytocin and carbetocin Timepoint: Baseline, 1,3,5,10 minutes and every 2nd minute following delivery of baby till 20 minutes	—

Countries

India

Contacts

Public ContactArun Kumar R

PSG Institute of Medical Sciences and Research

shivaaniarun76@gmail.com9944113440

Outcome results

None listed

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