Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients aged between 18-60 years of either gender, giving valid informed and written consent. Patients belonging to American Society of Anesthesiology(ASA) grade I, and II.
Exclusion criteria
Exclusion criteria: Participants with a history of allergy to any of the study drugs. Hemodynamically unstable participants. Patients taking analgesics before surgery Participants with difficult venous cannulation with 18G IV cannula satisfactorily in any large peripheral vein of the hand. Pregnant women
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate pain on injection of fentanyl and lignocaine pre-treatment for pain caused by propofol injection using 4 point pain scoreTimepoint: After 10 seconds | — |
Secondary
| Measure | Time frame |
|---|---|
| To study pain, edema, wheal and flare of patients who received fentanyl and lignocaine pre-treatment for pain caused by propofol injection.Timepoint: After one hour of induction.;To study patient satisfaction score of patients who received fentanyl and lignocaine pre-treatment for pain caused by propofol injection.Timepoint: After extubation | — |
Countries
India
Contacts
Guru Gobind Singh Medical College Hospital