Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: ASA grade I - II Patients undergoing FESS , rhinoplasty and septoplasty
Exclusion criteria
Exclusion criteria: patient refusal patient expected to require postoperative ventilation allergy to study drugs clinically significant cardiac arrhythmias pregnancy, breastfeeding significant renal/hepatic dysfunction psychiatric instability
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the effects of IV Remifentanil and IV Fentanyl on postoperative sedation and respiratory depression in Functional Endoscopic Sinus Surgery (FESS) surgery ,Rhinoplasty and SeptoplastyTimepoint: Post extubation of endotracheal tube the Modified Aldrete Score at 1,5,15 minutes will be recorded to measure postoperative respiratory depression and sedation Time taken from the administration of reversal agent till time of extubation will be recorded . | — |
Secondary
| Measure | Time frame |
|---|---|
| To compare surgical field satisfaction score & pain score when using IV Remifentanil & IV Fentanyl in Functional Endoscopic Sinus surgery ,Rhinoplasty & SetoplastyTimepoint: Pain score using visual analogue scale at 15,30 minutes will be recorded Post closure surgical field satisfaction by surgeon using likert score on scale of 1-5 | — |
Countries
India
Contacts
P D Hinduja Hospital and Medical Research Centre Mahim