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Reduction of pain on propofol injection after 6% Hydroxyethyl starch

Phase 3
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2024/01/061670
Lead Sponsor
JLN medical College
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

Patients undergoing elective surgery under general anaesthesia

ASA class 1 and 2

Exclusion Criteria

Patients undergoing emergency surgery

Patients in whom hand or forearm veins are not accessible

Patients with comorbidites

Patient refusal

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain during propofol injection <br/ ><br>Post operative pain recallTimepoint: Assessment of pain during propofol injection by Mc Crimick and hunter scale degree of pain during 2,5,10,20 seconds
Secondary Outcome Measures
NameTimeMethod
Haemodynamic changes <br/ ><br>To compare the severity of propofol injection painTimepoint: Baseline, 5minutes, 10 minutes, 20 minutes
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