A study to evaluate the safety and efficacy of two different doses of oxytocin bolus doses in elective caesarean sections.
Not Applicable
- Registration Number
- CTRI/2022/05/042453
- Lead Sponsor
- Department of Anaesthesia
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA grade II, Elective LSCS under Spinal Anaesthesia, Singleton pregnancy
Exclusion Criteria
•Refusal of patient
•Emergency LSCS
•History of allergy to oxytocin
•Placenta previa/accreta
•Polyhydramnios
• >2 Previous Caesarean sections
•Multifetal Pregnancy
•Contra-indications for Spinal Anaesthesia
•Inadequate Spinal Anaesthesia or conversion to General Anaesthesia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method