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 yet recruiting
- Conditions
- Medical and Surgical,
- Registration Number
- CTRI/2021/08/035362
- Lead Sponsor
- J Sivagurunathan
- Brief Summary
Aim of the study is to reduce the incidence and severity of propofol injection pain in patients undergoing surgery under general anaesthesia
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- All
- Target Recruitment
- 50
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 anaesthesia 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 anaesthesia 30 seconds after giving study drug
Trial Locations
- Locations (1)
Chettinad Hospital and Research Institute
🇮🇳Kancheepuram, TAMIL NADU, India
Chettinad Hospital and Research Institute🇮🇳Kancheepuram, TAMIL NADU, IndiaJ SivagurunathanPrincipal investigator8248310015sivagurunathanj@gmail.com