Methods of pain control for patients undergoing caesarean delivery
Phase 3
Completed
- Conditions
- Health Condition 1: null- pregnant women
- Registration Number
- CTRI/2018/05/014048
- Lead Sponsor
- maulana azad medical college and lok nayak hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
1.Pregnant patients undergoing elective / emergency caesarean section.
2.Patient height 150 â?? 170 cms.
3.Caesarean section with pfannenstiel incision
Exclusion Criteria
1.Any contraindication to sub arachnoid block.
2.Any obvious spine deformity.
3.ASA grade III/IV
4.Known h/o hypersensitivity to bupivacaine.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time to the first rescue analgesia in TAP block is higher than the wound site infiltrationTimepoint: The mean time to first rescue analgesia in Group T was 13.40±4.51 hours and in Group I was 6.20±4.25 hours which was statistically highly significant (p-0.001)
- Secondary Outcome Measures
Name Time Method 1.Patient pain will be evaluated by NPS at2,4,6,12,24hr after the block <br/ ><br>2.Total no. of doses of first rescue analgesics over 24 hr <br/ ><br>3.Total number of patients requiring second rescue analgesic. <br/ ><br>4.ComplicationTimepoint: The mean NPS score in group T was less as compared with group I <br/ ><br>2. Total number of doses of first rescue analgesic required over 24 hours was less in group T (0.967±0.18) as compared to group I (1.567±0.56 ) <br/ ><br>3. In our study only five patients in group I needed second rescue analgesic for pain control while none of the patients required second rescue analgesic in group T. <br/ ><br>4. none of the patients in our study had any complications.