Effect of TAP block to manage pain after caesarean sectio
Phase 4
- Conditions
- Health Condition 1: - Health Condition 2: 1- ObstetricsHealth Condition 3: 1- Obstetrics
- Registration Number
- CTRI/2024/02/063070
- Lead Sponsor
- Siddaganga medical college and research institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All women admitted for caesarean section under spinal anaesthesia
With age 21-40
Body mass index 19-30kg/m2
Haemoglobin level more than 9gm/dl
Exclusion Criteria
Women who fail to give consent
Women with comorbidities -epilepsy, heart disease, psychological disease
Women with intra-op complications- postpartum haemorrhage
Women with postoperative complications
Women with known allergy to any drugs
Women on analgesics
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess whether TAP block results in a clinically significant reduction in postoperative pain after caesarean delivery during first 24 hoursTimepoint: To assess whether TAP block results in a clinically significant reduction in postoperative pain after caesarean delivery at 2 hours, 4 hours, 6 hours, 8 hours, 12 hours, 18 hours, 24 hours
- Secondary Outcome Measures
Name Time Method 1. First rescue dose of analgesiaTimepoint: Less than 4 hours or after 4 hours;Number of extra doses of analgesia requiredTimepoint: Till 24 hours post delivert;Side effects of TAP reportedTimepoint: Till 24 hours;Time of first ambulationTimepoint: Less than 6 hours or more than 6 hours