Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients belonging to American society of Anaesthesiology grade I and II 2. Age between 18-60 years 3. Either sex 4. Patients posted for elective surgery under general anaesthesia of duration 1-3hrs
Exclusion criteria
Exclusion criteria: 1.Patients with obesity (BMI >55kgm-2) 2.Patients with history of allergy to test drug 3.Patients with history of hepatic and renal dysfunction 4.Patients with history of psychological disorders 5.Patients with history of alcohol and drug abuse 6.Patients with Heart rate 7.Refusal to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare and study the effectiveness of two doses of intravenous dexmedetomidine in alleviating pain on propofol injection. To note down changes in HR and MAP.Timepoint: Assessment of patients’ motor and verbal reactions, from time of propofol injection to loss of consciousness. HR and MAP will be noted : 1.Immediately before injection of study drug 2.pre-induction 3.post-induction 4.pre-intubation 5.post-intubation. | — |
Secondary
| Measure | Time frame |
|---|---|
| To note the side effects of intravenous dexmedetomidine if any.Timepoint: To note the side effects of intravenous dexmedetomidine if any during the induction and intraoperatively | — |
Countries
India
Contacts
Pt. B.D. Sharma PGIMS, Rohtak