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Clinical Trials/CTRI/2024/01/061575
CTRI/2024/01/061575
Not yet recruiting
Phase 2/3

A Prospective Randomized Comparative study of the effect of intravenous Lidocaine versus Dexamethasone on Propofol injection pain

Department of Anaesthesiology1 site in 1 country66 target enrollmentStarted: January 28, 2024Last updated:

Overview

Phase
Phase 2/3
Status
Not yet recruiting
Sponsor
Department of Anaesthesiology
Enrollment
66
Locations
1
Primary Endpoint
Verbal Numerical Rating scale

Overview

Brief Summary

This study is a prospective randomized double blind control study to compare the effect of intravenous Lidocaine 40mg or intravenous Dexamethasone 8mg in reducing the pain on injection of Propofol in patients undergoing elective surgeries under General Anaesthesia in KR Hospital

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Participant and Investigator Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • ALL ASA Grade I AND II patients undergoing elective Surgeries under General Anaesthesia.

Exclusion Criteria

  • All ASA grade III and IV patients Cardiovascular, respiratory and neurological disorders Patients allergic to Propofol and study drugs(soya bean oil,MCT,glycerol,egg lecithin and sodium oleate) Patients in whom hand or forearm veins not accessible Patients having problems in communication.

Outcomes

Primary Outcomes

Verbal Numerical Rating scale

Time Frame: assessed 50 seconds after intravenous injection of Propofol

Secondary Outcomes

  • Mc Crirrick & Hunter pain intensity scale(After 50 seconds of intravenous injection of Propofol before patient loses consciousness)

Investigators

Sponsor
Department of Anaesthesiology
Sponsor Class
Government medical college
Responsible Party
Principal Investigator
Principal Investigator

Aparna P

Mysore Medical College and Research Institute

Study Sites (1)

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