TO MEASURE THE EFFECT OF REDUCTION IN PAIN ON PROPOFOL INJECTION AFTER ADMINISTRATION OF 6% HYDROXYETHYL STARCH VS 2% LIDOCAINE.
Phase 3
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/07/055719
- Lead Sponsor
- Dr Merlyn Varghese
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.adult patient with ASA 1 and 2 class
2.patients between the age group 18-55 years old, of either gender
3.patients undergoing elective surgery under general anaesthesia
Exclusion Criteria
1.All emergency surgeries
2.ASA class 3 and 4
3.Paediatric population
4.pregnant individuals
5.known history of allergy to propofol or HES
6.presence of severe left ventricular dysfucntion
7.hand or forearm veins not accessible
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method