This study aims to compare 2 facial plane blocks using local anesthestic drug in providing pain free period in patients undergoing abdominal surgeries under general anesthesia
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/06/069573
- Lead Sponsor
- Dr Priyanka D S
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.patient willing to give informed written consent
2.American society of anesthesiologist grade 1 and 2 , 3.scheduled to undergo elective upper abdominal surgeries under general anesthesia (epigastric herniotomy, gastrectomy,open cholecystectomy, gastric perforation repair)
Exclusion Criteria
1. Patient refusal to give informed written consent 2. Allergy to local anesthetics
3. Infection at the site of injection 4.coagulopathy.5.prolonged opioid medication 6.chronic liver disease, chronic renal disease and cognitive impairment
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.Duration of post operative analgesia <br/ ><br>2.Time for requirement of first rescue analgesia <br/ ><br>3.post operative pain scores(VAS Scores) <br/ ><br>4. Total consumption of rescue analgesia in 24 hoursTimepoint: Immediate postoperative period, 2 hours, 6 hours 12 hours 24 hours
- Secondary Outcome Measures
Name Time Method Hemodynamic monitoring <br/ ><br>Timepoint: Immediate postoperative period,1,2,6,12,24 hours after tracheal extubation