Health Condition 1: null- ASA physical status I and II posted for nasal surgeries
Conditions
Interventions
Intervention1: Group I - Inj dexmedetomidine: Group I would receive Inj dexmedetomidine as 0.5 mcg/kg by intravenous route over 15 minutes and then 0.1mcg/kg/hr as infusion
Control Intervention1: Gr
Sponsors
Shri Sathya Sai Medical College and Research Institute
Eligibility
Inclusion criteria
Inclusion criteria: 1.Posted for nasal surgeries 2.ASA physical status I and II 3. Elective surgeries
Exclusion criteria
Exclusion criteria: 1. ASA physical status III and above 2. Heart disease and rhythm disturbances 3. psychiatric illness and anxiety disorder 4. History of post traumatic stress disorder 5. Emergency surgeries 6. Pregnancy 7. History of obstructive sleep apnea
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare incidence of emergence agitation between Inj Dexmedetomidine and Inj Midazolam group.Timepoint: At regaining consciousness, at extubation, every 5 minutes till 30 minutes are over | — |
Secondary
| Measure | Time frame |
|---|---|
| To compare perioperative vitals, sedation and recovery profileTimepoint: At baseline, at 5 minutes, at 15 minutes after starting drug infusion then every 15 minutes till end of surgery. sedation and recovery profile at return of consciousness, at extubation and then every 5 minutes for 30 minutes. | — |
Countries
India
Contacts
Public ContactDr Pranjali Kurhekar
Shri Sathya Sai Medical College and Research Institute
Outcome results
None listed