Health Condition 1: - Health Condition 2: O- Medical and Surgical
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Adult patients between 18-65 years of age 2.Patients undergoing elective surgery under general anesthesia with controlled ventilation. 3.Patients of ASA status 1 and 2.
Exclusion criteria
Exclusion criteria: 1.Patients not giving consent 2.Obesity (BMI > 30Kg/m2) 3.Patients receiving any medications likely to affect Propofol requirement or hemodynamic parameters. 4.History of allergy to eggs and Study drugs 5.Anticipated difficult intubation. 6.Pregnant and lactating women
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| SECONDARY OUTCOME : PAIN ON PROPOFOL INJECTIONTimepoint: AT 0, 3 AND 5 MINUTES | — |
Primary
| Measure | Time frame |
|---|---|
| PRIMARY OUTCOME : 1.DOSE REQUIREMENT OF PROPOFOL. 2.HEMODYNAMIC PARAMETERS - HEART RATE , BLOOD PRESSURE . Timepoint: 1.DOSE OF PROPOFOL AT LOSS OF VERBAL RESPONSE . 2.HEART RATE AND BLOOD PRESSURE AT BASELINE , IMMEDIATELY AFTER FENTANYL INJECTION ,IMMEDIATELY AFTER PROPOFOL INDUCTION AND AFTER INTUBATION AND THEREAFTER EVERY 3 MINUTES FOR NEXT 15 MINUTES. | — |
Countries
India
Contacts
PUSHPAGIRI INSTITUTE OF MEDICAL SCIENCES AND RESEARCH CENTRE