MedPath

Post operative pain relief in comparison with block with spinal

Phase 2
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2023/08/056122
Lead Sponsor
Vijayanagara Institute Of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1. ASA Physical status I and II

2. Patients posted for elective PCNL surgeries

3. Patients who can understand and rate their pain on NRS Scale

Exclusion Criteria

1. Refusal by patients for the procedure

2. History of significant systemic disorder

3. Infection at block site or spinal injection site

4. Thorasic wall and chest wall deformities

5. Allergy to test drugs

6. Patients on chronic use of analgesics

7. Patients on morbid obesity

8. Bleeding disorders

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Duration of post operative analgesiaTimepoint: After surgery 5min, 10min, 20min, 30min, 60min, 120min
Secondary Outcome Measures
NameTimeMethod
1.To asses the cumulative consumption of analgesia for 24 hours in post operative period <br/ ><br>2.Dermatomal sensory levels and grading of motor blockade before General Anaesthesia and postoperatively following extubation. <br/ ><br>3.To evaluate pain at rest at serial intervals post operatively using Numerical Rating Scale (NRS) <br/ ><br>4.Comparison of haemodynamic parameters (Heart rate, systolic and diastolic blood pressure, mean arterial blood pressure) in intra operative period. <br/ ><br>5.Incidence of postoperative nausea and vomiting upto 24 hours <br/ ><br>6.Patient satisfaction score <br/ ><br>7.Adverse effects, if any <br/ ><br> <br/ ><br>Timepoint: 24hours
© Copyright 2025. All Rights Reserved by MedPath