A Clinical Trial To Study Postoperative Pain By Comparing Block Versus Infiltration Technique In Laparoscopic Cholecystectomy Patients.
Phase 4
- Conditions
- Health Condition 1: K802- Calculus of gallbladder without cholecystitis
- Registration Number
- CTRI/2024/01/061302
- Lead Sponsor
- Sri Narayani Hospital And Research Centre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
American Society Of Anaesthesiology 1 and 2
Exclusion Criteria
Patient Refusal American Society Of Anaesthesiologists Morethan 3
Allergic To Amide Local Anesthetics Or Medications Included In Study
Infection At The Needle Insertion Site
Pregnant Women
Body Mass Index Morethan 35
Drug Abusers
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The Assessment of Duration of Post Operative AnalgesiaTimepoint: 24 hours
- Secondary Outcome Measures
Name Time Method Total Analgesic Required in 24 hours Intraoperative and Postoperative Opioid ConsumptionTimepoint: 24 hours