Portal Blocks for relief of postoperative pain in patients undergoing Cesarean sectio
Phase 2
- Conditions
- Health Condition 1: O82- Encounter for cesarean delivery without indication
- Registration Number
- CTRI/2024/02/062211
- Lead Sponsor
- Dr Ravi Kerur
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA physical status I and II.
Age between 20 to 40 years.
Weight ranging from 70-90kg
Height ranging from 155-185cm (5ft to 6ft)
Patients undergoing LSCS under spinal anesthesia
Provides Consent
Exclusion Criteria
Patient who refuse to give consent.
Patient with obstetric complications
Patient with suspected fetal compromise
Coagulopathy
Patients who do not fulfill inclusion criteria.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate efficacy of portal blocks for post-operative pain management in woman undergoing Cesarean section using NRS scores for assessment of pain.Timepoint: At Baseline before administration of block, then 20 min after block then 1hr,2hr,3hr,4hr,5hr,6hr,24hr,48hr after the block
- Secondary Outcome Measures
Name Time Method To Evaluate patient satisfaction, effects on hemodynamic parametersTimepoint: At Baseline before administration of block, then 20 min after block then 1hr,2hr,3hr,4hr,5hr,6hr,24hr,48hr after the block