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Safest effective dose of oxytocin to avoid bleeding from uterus during cesarean section.

ED90 of Prophylactic Oxytocin Infusion During Cesarean Delivery in Laboring Preeclamptics receiving Magnesium Sulfate Therapy versus Normotensives: An Up-Down Sequential Allocation Dose-Response Study - None

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/05/019267
Enrollment
80
Registered
2019-05-22
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: O754- Other complications of obstetric surgery and procedures

Interventions

Intervention1: In Preeclamptic pregnant patients with magnesium sulfate therapy: Titrated dose of intravenous oxytocin infusion: The dose of the infusion will be 18 IU/h (i.e., 0.29 IU/min) for the fi

Sponsors

UCMS and GTBH
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All laboring parturients >18 years age who have received oxytocin for labor induction and/or augmentation, whether preeclamptics who are receiving magnesium sulfate therapy (posted for cesarean section under spinal block/general anaesthesia) or normotensives without magnesium sulfate therapy( posted for cesarean section under spinal block) will be enrolled.

Exclusion criteria

Exclusion criteria: Exclusion criteria will include patient refusa, history of PPH or more than one previous uterine surgery as well as bleeding disorders, and presence of abnormal placentation, uterine fibroid. Those with any contraindication to spinal block such as hemodynamic instability, infection at site of injection, coagulopathy (thrombocytopenia with platelet count <100,000/mm3) etc. will also be excluded

Design outcomes

Primary

MeasureTime frame
The calculated ED90 of prophylactic oxytocin infusion in both cohorts.Timepoint: The status of uterine tone assessed by the operating obstetrician (satisfactory or unsatisfactory) at 4-minute post-oxytocin initiation.

Secondary

MeasureTime frame
The requirement of additional uterotonic drugs.Timepoint: From cord clamping to end of surgery.

Countries

India

Contacts

Public ContactDr Asha Tyagi

Department of Anaesthesiology and Critical Care

drashatyagi@gmail.com

Outcome results

None listed

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