Study comparing injection at two separate points for pain relief after after cesarean delivery
Not Applicable
- Conditions
- Health Condition 1: O82- Encounter for cesarean delivery without indication
- Registration Number
- CTRI/2020/11/029353
- Lead Sponsor
- Medica Superspecialty Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA 2 females
Age between 18-40 yrs
Normal singleton pregnancy with gestational age of
37 weeks
Scheduled for elective cesarean section by
Pfannensteil incision
Exclusion Criteria
Emergency surgery
Patients not willing to participate in the study
Conversion to general anesthesia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 24 hrs opioid consumptionTimepoint: 24 hrs opioid consumption
- Secondary Outcome Measures
Name Time Method VAS score at rest,on movement,extent of sensory block, level of nausea, vomiting, sedationTimepoint: 1,4,6,12 and 24hrs