MedPath

A comparative study of pain management techniques for surgeries of the backbone

Phase 4
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2024/02/062635
Lead Sponsor
Manipal Hospital Whitefield
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

American Society of Anaesthesiologists physical status 1 - 3

Exclusion Criteria

Patients who are allergic to local anaesthetics.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
24-hour postoperative pain scores using Numeric Rating Scare (NRS 0 - 10)Timepoint: Baseline (0 hour in the postoperative period); 2 hours; 4 hours; 8 hours; 12 hours, 24 hours in the postoperative period
Secondary Outcome Measures
NameTimeMethod
To compare the number of rescue analgesics needed between patients receiving and not receiving Erector spinae plane block for elective lumbar spine surgery under general anaesthesia.Timepoint: 24 hours after surgery;To compare the patients pain control satisfaction between patients receiving and not receiving Erector spinae plane block for elective lumbar spine surgery under general anaesthesia.Timepoint: 24 hours after surgery
© Copyright 2025. All Rights Reserved by MedPath