Comparison between two different nerve blocks for post operative pain relief.
Phase 2
- Conditions
- Health Condition 1: O998- Other specified diseases and conditions complicating pregnancy, childbirth and the puerperium
- Registration Number
- CTRI/2022/05/042383
- Lead Sponsor
- Dr Anil Salesh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Pregnant patients coming for elective or emergency LSCS
2. American Society of Anaesthesiologists (ASA) physical status classes II
3. Age :18â??40 years
Exclusion Criteria
BMI > 35 kg/m2
Weight less than 50kg
Known allergy to local anaesthetics
Coagulopathies
Raised intracranial pressure
Local infection at site of injection
History of heart block, dysrhythmias, neurological diseases
Patient refusal
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the duration of analgesic effect between the blocks, measured as time from administration of block to request of first rescue analgesic or first VAS score more than 4. <br/ ><br>Timepoint: To compare the duration of analgesic effect between the blocks, measured as time from administration of block to request of first rescue analgesic or first VAS score more than 4. <br/ ><br>
- Secondary Outcome Measures
Name Time Method To compare total analgesic requirement in doses postoperatively in first 24hrs <br/ ><br>To compare VAS score at time points (0,30mins,1hr,2nd hr,4th hr,6th hr, 8th hr,12th hr,24hrs) <br/ ><br>Timepoint: 0,30mins,1hr,2nd hr,4th hr,6th hr, 8th hr,12th hr,24hrs