A clinical trial to study the comparison of two different nerve blocks for pain relief in patients undergoing upper abdominal surgery
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/02/050011
- Lead Sponsor
- All India Institute of Medical Sciences, Patna
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA I â??II patients scheduled to undergo elective supra-umbilical surgeries with unilateral
incision under GA
Exclusion Criteria
1.BMI < 20
2.Allergy to local anesthetics
3.Infection at the site of injection
4.Chronic pain syndromes
5. Patients on chronic analgesic therapy
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 Time to first rescue analgesic administrationTimepoint: Time to first rescue analgesic administration
- Secondary Outcome Measures
Name Time Method Time of block performance (TBP) <br/ ><br> Intraoperative fentanyl consumption <br/ ><br> Amount of postoperative Fentanyl consumption in first 24 hours <br/ ><br>Postoperative pain score evaluated by NRS at 0,1,2,4, 6, 12 and 24 hrs. <br/ ><br>Complications <br/ ><br>Timepoint: 0,1,2,4, 6, 12 and 24 hrs.