A Comparative study to decrease incidence of pain on injection of propofol using newer preparations of propofol emulsion.
Not Applicable
Completed
- Conditions
- Health Condition 1: null- children aged 6-12years under ASA 1 and 2 undergoing any elective surgical procedure under general anaesthesia
- Registration Number
- CTRI/2018/01/011562
- Lead Sponsor
- Vijayanagar Institute of Medical Sciences Ballari
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 100
Inclusion Criteria
ASA 1 and ASA 2 patients
Exclusion Criteria
ASA 3 and 4 patients
co existing systemic disease
contra indication to propofol
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the effect of 0.5% dilution of propofol MCT/LCT with propofol LCT for injection pain during induction of general anaesthesia (GA) in paediatric patients.Timepoint: 15 seconds, 30 seconds and 1 minute intervals.
- Secondary Outcome Measures
Name Time Method To compare the effect of 0.5 % dilution of propofol MCT/LCT with propofol LCT on haemodynamic changes during induction of GA in both the groups.Timepoint: 15 seconds, 30 seconds and further at 1 minute intervals upto 5 minutes after induction