A study to compare the efficacy of erector spinae block and quadratus lumborum block for pain management in kidney transplant donors after sugery.
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/04/041599
- Lead Sponsor
- Sishir Siwakoti
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Laparoscopic donor nephrectomy patients
ASA class I and II
Exclusion Criteria
Patient unacceptance.
Local infection of the skin where block is to be given.
History of allergy to the local anesthetic agents used in this study.
Patients with history of coagulation disorder or if patient is under any anticoagulant drugs.
End-stage organ and system failure, severe pulmonary and/or cardiovascular problem.
Substance addiction or known psychiatric or mental problems.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome of this trial is cumulative morphine consumption over 24 hours <br/ ><br>Timepoint: 1, 3, 6, 12 and 24 hours after surgery
- Secondary Outcome Measures
Name Time Method Evaluation of pain: NRS score for pain in the first postoperative 24h. <br/ ><br>Timepoint: 1, 3, 6, 12 and 24 hours after surgery. <br/ ><br>;Hemodynamic profile of the patient, namely heart rate and Mean Arterial pressureTimepoint: 1, 3, 6, 12 and 24 hours after surgery. <br/ ><br>;Intervention-related complications including hematoma, organ injuries, and lower extremity weakness, vascular puncture, kidney injury in the interventional group. <br/ ><br>Timepoint: 1, 3, 6, 12 and 24 hours after surgery. <br/ ><br>