comparing the analgesic effect between a local anaesthetic and a drug used for induction in alleviating the pain caused while administering a lipid emulsion drug during induction of general anaesthesia.
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2021/08/035362
- Lead Sponsor
- J Sivagurunathan
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA PS 1 and 2 patients undergoing surgeries under general anaesthesia
Exclusion Criteria
Patient refusal study
Known allergy for study drug
Pregnant females
Cardiovascular diseases, renal and hepatic dysfunctions
ASA PS 3 and 4
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To reduce the incidence of propofol injection pain in patients undergoing surgery under general anaesthesiaTimepoint: 30 seconds after giving study drug
- Secondary Outcome Measures
Name Time Method To reduce the severity of propofol injection pain in patients undergoing surgery under general anaesthesiaTimepoint: 30 seconds after giving study drug