Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: Total Intravenous Anaesthesia: Propofol intravenous infusion (Target controlled Infusion for a plasma concentration of 3-5 microgram per ml)
Control Intervention1: Inhalational Anaesthe
Sponsors
Amrita Institute of Medical Sciences and Research Centre
Eligibility
Inclusion criteria
Inclusion criteria: Patients of age >18 and ASA 1 and 2 physical status Elective posterior cranial fossa (infratentorial) surgeries
Exclusion criteria
Exclusion criteria: ASA 3 and 4 physical status Emergency craniotomy Preoperative GCS Patients regularly on anti-emetics Patients extubated >2h after surgery completion
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Post-operative Nausea and vomiting as assessed by PONV Impact scaleTimepoint: 24 hours post-operatively | — |
Secondary
| Measure | Time frame |
|---|---|
| to compare the recovery characteristics of patients receiving inhalational anaesthesia versus Total Intravenous AnaesthesiaTimepoint: GCS will be assesses at 0.5 hours, 1 hour and 6 hours post-operatively | — |
Countries
India
Contacts
Public ContactDr Avanthi Subramanian
Amrita Institute of Medical Sciences and Research centre
Outcome results
None listed