None listed
Conditions
Interventions
Intervention1: Propofol induction with priming: 1-2mg/kg total dose,20% of this given as priming dose, speed of injection
30 mg over 10 seconds
Control Intervention1: Propofol induction without priming: 1-2 mg/kg total dose, speed of injection 30mg/sec
Sponsors
Nil
Eligibility
Inclusion criteria
Inclusion criteria: American Society of Anesthesiology Physical status class I [healthy patient] or class II [mild systemic disease] patients in the age group 18-55 yrs of age posted for elective surgery.
Exclusion criteria
Exclusion criteria: Pregnant and lactating women Patients allergic to study medications Patients with uncorrected hypotension Patients with valvular heart disease.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction in dose requirement as evidenced by successful anesthesia with less dose.Timepoint: Successful anesthesia is defined by the time point when there is loss of verbal response of the patient. | — |
Secondary
| Measure | Time frame |
|---|---|
| Hemodynamic stability as evidenced by proportion of subjects with blood pressure and heart rate fluctuation within 15% of mean.Timepoint: BP and heart rate,30 mins prior to surgery,just before induction of anesthesia,1 min after induction,immediately after intubation and 5 mins after induction | — |
Countries
India
Contacts
Public ContactDr Unnikrishnan P
Outcome results
None listed