A scientific experiment to evaluate and compare the efficacy of intravenous Lidocaine and Dexamethasone in terms of attenuation of Propofol injection pain during induction of Anaesthesia
Phase 2
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/01/061575
- Lead Sponsor
- Department of Anaesthesiology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
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
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Verbal Numerical Rating scaleTimepoint: assessed 50 seconds after intravenous injection of Propofol
- Secondary Outcome Measures
Name Time Method Mc Crirrick & Hunter pain intensity scaleTimepoint: After 50 seconds of intravenous injection of Propofol before patient loses consciousness