To compare effect of two different pain relieving blocks in patients undergoing laparoscopic inguinal hernia surgery
Phase 4
Completed
- Conditions
- Health Condition 1: K402- Bilateral inguinal hernia, withoutobstruction or gangreneHealth Condition 2: K409- Unilateral inguinal hernia, without obstruction or gangrene
- Registration Number
- CTRI/2020/02/023230
- Lead Sponsor
- Department of Anaesthesia and intensive care
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 42
Inclusion Criteria
ASA I - II
Patient scheduled for elective laparoscopic inguinal hernia surgery
Exclusion Criteria
BMI > 40kg/m2
Coagulopathy
Allergic to Ropivacaine, paracetamol and diclofenac
Pregnant and lactating women
Substance abuse
Not able to understand VAS score
Contraindication to general anaesthesia or laparoscopic surgery
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method