Skip to content

Safe dose of oxytocin to control excessive bleeding from uterus during cesarean section in patients with body weight above normal

ED90 of Prophylactic Oxytocin Infusion During Cesarean Delivery in Non-laboring Obese vs. Non-Obese Patients: An Up-Down Sequential Allocation Dose- Response Study - None

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/05/042469
Enrollment
80
Registered
2022-05-11
Start date
Unknown
Completion date
Unknown
Last updated
2023-02-06

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 Non-laboring Obese patients: Titrated dose of intravenous oxytocin infusion: The dose of the infusion will be 13IU/h(0.22IU/min) for the first patient.Dosing interval (increase) for

Sponsors

UCMS and GTBH
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All non-laboring parturient >18 years age will be enrolled. The two arms will include obese (body mass index >=30 kg/m2) or non-obese pregnant patients (body mass index

Exclusion criteria

Exclusion criteria: Exclusion criteria shall be patient refusal, presence of labor (defined as cervical dilatation of 3 cm or more), use of oxytocin in the preoperative period, history of PPH or more than one previous uterine surgery as well as bleeding disorders, presence of abnormal placentation and uterine fibroid, contraindications to spinal block, such as hemodynamic instability, infection at the injection site, and coagulopathy (thrombocytopenia with platelet count 1.5).

Design outcomes

Primary

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

Secondary

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

Countries

India

Contacts

Public ContactDr Asha Tyagi

University College of Medical Sciences and GTB Hospital

drashatyagi@gmail.com

Outcome results

None listed

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