None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.age between 18-65 years 2.ASAPS I, II III 30. Patients scheduled for surgeries under general anaesthesia. 3. Minimum duration of surgery lasting more than 180 minutes.
Exclusion criteria
Exclusion criteria: 1. Patients unwilling to participate in the study. 2. Patients who are unable to give informed consent. 3. Patients with known history of psychiatric illness, chronic drug or alcohol abuse. 4. Patients with known hypersensitivity to drugs used. 5. Pregnant and lactating women. 6. BMI>30kg/m 2 . 7. Patients on concurrent sedative medications. 8. Patients who are unable to attempt or perform the DSST test.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| to compare the psychomotor recovery profile of patients receiving either IV dexmedetomidine bolus (Group D) or subanaesthetic ketamine bolus (Group K) by Digit Symbol Substitution Test (DSST) postoperatively at 15,30,60,90,120 minutes post extubationTimepoint: to compare the psychomotor recovery profile of patients receiving either IV dexmedetomidine bolus (Group D) or subanaesthetic ketamine bolus (Group K) by Digit Symbol Substitution Test (DSST) postoperatively at 15,30,60,90,120 minutes post extubation | — |
Secondary
| Measure | Time frame |
|---|---|
| additional boluses of fentanyl givenTimepoint: intraoperatively;propofol boluses givenTimepoint: intraoperatively;to Compare Postoperative sedationTimepoint: 15,30,60,90,120 minutes postoperatively;time to first request of analgesiaTimepoint: postoperatively;hemodynamic changesTimepoint: post induction immediately | — |
Countries
India
Contacts
Sri venkateswara institute of medical sciences