MedPath

Real-time ultrasonography guided Erector Spinae Block for Laparoscopic Live Donor kidney transplant - A Randomised Controlled Trial

Not Applicable
Registration Number
CTRI/2021/09/036208
Lead Sponsor
Postgraduate Institute of Medical Education and Research Chandigarh
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

ASA I-II patients, scheduled to undergo laparoscopic live donor nephrectomy under general anaesthesia will be enrolled in this study

Exclusion Criteria

Exclusion criteria include Local infection at the site of block, Patient denial, Psychiatric illness, Allergy to local anaesthetics.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
cumulative opioid consumption in the first 24 hours after surgery.Timepoint: cumulative opioid consumption in the first 24 hours after surgery.
Secondary Outcome Measures
NameTimeMethod
1.VNRS scores for pain at 0 h (extubation), 3 h, 6 h, 12 h, 24 h. <br/ ><br>2.Time to first rescue therapy. <br/ ><br>3.Incidence and severity of postoperative nausea and vomiting, local anesthetic toxicity. <br/ ><br>4.Duration of hospital stay. <br/ ><br>5.Patient satisfaction score. <br/ ><br>6.Complications related to the procedure <br/ ><br>7.Dynamic VNRS scores ( pain score during cough) at 3, 6, 12, 24 hours <br/ ><br>8.Time to ambulation <br/ ><br>Timepoint: 0 to 24 hours
© Copyright 2025. All Rights Reserved by MedPath