Health Condition 1: K20-K31- Diseases of esophagus, stomach and duodenum Health Condition 2: H65-H75- Diseases of middle ear and mastoid
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. American Society of Anesthesiologists (ASA) physical status I and II 2. Patients undergoing any elective surgeries under General Anesthesia 3. Patients giving informed valid written consent
Exclusion criteria
Exclusion criteria: 1. Patients refusing to give consent 2. Patients posted for emergency surgeries 3. Patients with anticipated or actual difficult airway 4. Patients with cardiac, renal, hepatic, cerebral diseases 5. Patients allergic to Propofol and / or fentanyl 6. Patients with BMI 30kg/m2 7. Patients with alcohol intake and drug (enzyme inducer) use
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To measure the total dose of Propofol required for induction of anesthesia following administration of Fentanyl at varying time intervals.Timepoint: Dose of Propofol required will be measured at the end of 1min, 3min and 5min. | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate the effect of varying time intervals between administration of Fentanyl and Propofol on hemodynamic variables such as hear rate, Systolic BP, Diastolic BP and Mean Arterial Pressure.Timepoint: HR, SBP, DBP, MAP, spo2 measured every minute upto 10 minutes. | — |
Countries
India
Contacts
Karnataka Institute of Medical Sciences