This study is being conducted to compare two methods of pain relief for cesarean section one of which involves giving an injection in the back and the other over sides of abdome
Not Applicable
- Conditions
- Health Condition 1: O998- Other specified diseases and conditions complicating pregnancy, childbirth and the puerperium
- Registration Number
- CTRI/2019/03/018103
- Lead Sponsor
- Kasturba Medical College student research fund
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All ASA II pregnant women in the age group of 18 to 40 years undergoing elective lower segment caesarean deliveries under subarachnoid block are included in the study
Exclusion Criteria
Patient refusal
Coagulation disorders
Local infection at the site of block
Allergy to study medications
BMI >35 kg/m2
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method a)Duration of analgesia (by noting down the demand for first analgesia) <br/ ><br>b)24 hour opioid (tramadol) consumption <br/ ><br>Timepoint: Every hour for the first 10 hours and 24 hrs postoperatively
- Secondary Outcome Measures
Name Time Method Patient satisfaction score from 1 to 10Timepoint: 24hours after the surgery