Health Condition 1: R688- Other general symptoms and signs
Conditions
Interventions
Intervention1: Fentanyl with propofol: 3 groups- A,B and C
Will receive propofol 3 minutes,5 minutes and 7 minutes after fentanyl administration
Control Intervention1: Additional propofol requirement
Sponsors
Government medical college Amritsar
Eligibility
Inclusion criteria
Inclusion criteria: 1.Patients age group between 18-65 years of either sex undergoing elective surgery under general anesthesia 2.American society of anesthesiology grade 1 and 2 3.Duration of Surgery under 2 hours
Exclusion criteria
Exclusion criteria: 1.patient refusal for written consent 2.Allergy to propofol and fentanyl 3.Undergoing emergency surgery 4.presence of cardiovascular, respiratory, hyperthyroidism, hypothyroidism, cerebrovascular disease or renal disease(including hypertension) 5.Anticipated difficult airway 6.History of alcohol and drug abuse
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the effect of varying time interval between fentanyl and propofol administration on propofol requirement for induction of anesthesiaTimepoint: Randomized group allocation Group A- patients will receive propofol 3 minutes after fentanyl administration Group B - patients will receive propofol 5 minutes after fentanyl administration Group C - patients will receive propofol 7 minutes after fentanyl administration | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.Hemodynamics responses in different groups 2.Additional propofol requirement 3.Adverse effect such as hypotension, bradycardiaTimepoint: Total dose of propofol requirement for induction after 3 minutes,5 minutes, 7 minutes & there heart rate,blood pressure changes noted post induction | — |
Countries
India
Contacts
Public ContactDr Anu Sharma
Government medical college Amritsar
Outcome results
None listed