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A study to do comparison between two drugs bupivacaine 0.5% ( Heavy ) with clonidine and ropivacaine 0.75% ( Heavy ) with clonidine in surgeries involving lower parts of the body by giving spinal anaesthesia

Phase 3
Conditions
Health Condition 1: 3- Administration
Registration Number
CTRI/2024/03/063415
Lead Sponsor
Bharti
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Any patients belongs to ASA grade I and II scheduled to undergo any major surgeries involving lower limbs and lower abdomen

Exclusion Criteria

ASA grade III and IV

BMI more and equal to 30

General contraindications to spinal anaesthesia

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Severity of Pain assessment using VAS pain scoreTimepoint: Intra-operatively every 30 minutes till the duration of surgery <br/ ><br>Post-operatively at 2, 4, 6, 8 and 12 hours
Secondary Outcome Measures
NameTimeMethod
1. Total requirement of Injection Tramadol <br/ ><br>2. Hemodynamic changes <br/ ><br>3. Post operative complications ( nausea, vomiting, hypotension, sedation ) <br/ ><br>4. Patient Satisfaction ScoreTimepoint: First 12 hours postoperatively
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