Health Condition 1: null- ASA 1 and ASA 2
Conditions
Interventions
Intervention1: Propofol MCT/LCT
(medium chain triglyceride/long chain triglyceride): 30 mg (3 cc) of propofol MCT/LCT injected intravenously over 20 sec
Control Intervention1: Propofol LCT: 3o mg (3 c
Sponsors
SDM College of Medical Sciences and Hospital
Eligibility
Inclusion criteria
Inclusion criteria: 1.The subjects who are aged between 18 to 60 years belonging to ASA Physical status 1 and 2. 2. Those willing to participate.
Exclusion criteria
Exclusion criteria: 1.Patients with ischaemic heart diseases, neurological or psychiatric problems, renal or hepatic insufficiency, suspected or known airway difficulty. 2. Pregnant or lactating women. 3. Those who were taking any analgesics before surgery. 4. Those with known hypersensitivity to propofol or to any of the constituents of emulsion. 5. Those who refuse to give consent.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| pain on propofol induction and pain recall postoperatively. Verbal rating scale for injection pain and recall pain used.Timepoint: Following 3cc of propofol induction pain will be assessed after 30 secs. Full dose of propofol will be given after assessing pain. Pain recall postoperatively 30 mins after the patient is shifted to post operative ward | — |
Secondary
| Measure | Time frame |
|---|---|
| changes in Pulse rate, Non invasive Blood pressure and SaturationTimepoint: pre induction, induction, postoperatively | — |
Countries
India
Contacts
Public ContactSupreeth R Shetty
Mandya institute of medical sciences
Outcome results
None listed