None listed
Conditions
Interventions
Control Intervention1: Desflurane: Group A participants will be given Desflurane inhalational anesthesia to maintain an adequate depth of anesthesia BIS 40 to 60 administered throughout the surgery as
Sponsors
Regional Institute of Medical Sciences
Eligibility
Inclusion criteria
Inclusion criteria: American Society of Anaesthesiologists ASA grade I and II scheduled for elective Lap cholecystectomy and is willing to participate in the study and has signed the informed consent form
Exclusion criteria
Exclusion criteria: Patient refusal , Pregnancy or lactation, history of malignant hyperthermia, severe cardio pulmonary disease, endocrine or renal disorders, obesity, neurological conditions and patients who have a history of severe allergic reactions to inhalational agents or other components of anesthesia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the time to emergence from Anesthesia between Desflurane and SevofluraneTimepoint: Time from cessation of anesthesia to patient first sign of consciousness starting from baseline to every 5 minutes post extubation till 30 minutes | — |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate hemodynamic stability during induction maintenance & emergency phases of anesthesiaTimepoint: Blood pressure pulse & oxygen saturation will be measured from baseline to first 1 hour in a 5 minute interval | — |
Countries
India
Contacts
Public ContactDr Y ARUNKUMAR SINGH
Regional Institute of Medical Sciences
Outcome results
None listed