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A clinical study comparing the effects of oxytocin administered at different rates during planned caesarean surgery.

Not Applicable
Conditions
Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Registration Number
CTRI/2022/09/046096
Lead Sponsor
All India Institute of Medical Sciences Patna
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Pregnant patients undergoing elective caesarean section in spinal anaesthesia will be included in the study.

1. Uncomplicated, singleton pregnancy

2. ASA class 1 & 2

Exclusion Criteria

1. Patients with multiple pregnancies

2. Complicated pregnancies, risk factors for postpartum haemorrhage (PPH)

3. Contraindication to spinal anaesthesia and

4. Patients in active labour.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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