Early iv oxytocin during emergency caeserean section in decreasing blood loss

A Randomised control trial of Efficacy of early IV oxytocin infusion at the time of Abdominal skin incision in decreasing blood loss in emergency primary caesarean section - NIL

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/04/065764

Enrollment

300

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: O721- Other immediate postpartum hemorrhage

Interventions

Intervention1: Oxytocin infusion: oxytocin 10 Units in 200ml of Ringer lactate intravenous infusion over 15 mins 250drops Control Intervention1: Oxytocin injection: oxytocin 10units intramuscular on

Eligibility

Inclusion criteria

Inclusion criteria: 1.Primi Singleton Pregnancy with 37 completed weeks of gestation taken up for Emergency primary caeserean section 2.Multiparous women with previous normal vaginal delivery / previous instrumental deliveries with 37 completed weeks of gestation who are taken up for Emergency Primary caesarean section

Exclusion criteria

Exclusion criteria: Obesity ,Heart disease, Gestational Hypertension, Gestational Diabetes mellitus on Insulin, Previous LSCS ,Previous Myomectomy ,Previous Laparotomy

Design outcomes

Primary

Measure	Time frame
Evaluate The Efficacy Of Early Iv Oxytocin Infusion In Primary Caeserean Section In Reduction Of Intraoperative And Post Operative Blood Loss And In Reduction Of Usage Additional Uterotonics Timepoint: 5 months	—

Secondary

Measure	Time frame
In This Study Intraoperative And Post Operative Haemorrhage Can Be Reduced And Hence Maternal Mortality Due To Pph Can Be ReducedTimepoint: 2 years	—

Countries

India

Contacts

Public ContactBHACKIYA

Government Thanjavur Medical college and hospital

rajidr_2003@yahoo.co.in9894616469

Outcome results

None listed

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