Study of comparison of different modes of analgesia for upper abdominal surgery
Not Applicable
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/05/052219
- Lead Sponsor
- Swati Singh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 117
Inclusion Criteria
1 Patient posted for upper abdominal surgery
2 Patients of ASA physical status 1, 2 & 3
Exclusion Criteria
1 Patient’s refusal to participate
2 Patients of ASA physical status 4
3 Any allergy to local anaesthetics/ opioids
4 Coagulation disorders
5 Infection at the site of intervention
6 History of any underlying cardiac, renal dysfunction
7 Pregnant patient
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Quality of recovery score (QoR)-15 scoreTimepoint: 24 hour postoperative
- Secondary Outcome Measures
Name Time Method 1.Numerical Rating Scale (NRS) Score at 2,4,8,12,24 hrs post op <br/ ><br>2.Postoperative complications in either groups <br/ ><br>3.Hemodynamic parameters <br/ ><br>4.Time to first rescue analgesia and total dose in first 24 hrs <br/ ><br>Timepoint: 2,4,8,12,24 hours