Health Condition 1: 4- Measurement and Monitoring
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients who have given written informed consent 2. Patients with ASA grade I & II. 3. Patients aged 18-60 years. 4. Patients with BMI 19-28 kg/m2 5. Patients scheduled for elective surgery under general anaesthesia.
Exclusion criteria
Exclusion criteria: 1. Patients not willing to give written informed consent. 2. Patients with history of allergy to dexmedetomidine.. 3. Patients with anticipated difficult mask ventilation/difficult intubation. 4. Patients with baseline heart rate 5. Patients with coronary heart disease, ischemic heart disease, heart blocks, diabetes mellitus. 6. Pregnant women/Breastfeeding mothers.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Dexmedetomidine nebulisation effectively attenuates pressor response to laryngoscopy and intubation when compared to dexmedetomidine given intravenously , efficacy parameter being hemodynamic parameters ( heart rate, systolic BP, diastolic BP, mean arterial pressures, SpO2Timepoint: Baseline Before drug After drug Before induction After induction Immediate after intubation 1 min after intubation 2 min after intubation 5 min after intubation 10 min after intubation | — |
Secondary
| Measure | Time frame |
|---|---|
| dexmedetomidine nebulisation may have lesser side effects like bradycardia, hypotension, dizziness ,post operative sedation etc.Timepoint: Intra-operative Post-operative till 2 hours | — |
Countries
India
Contacts
Bangalore Medical College and Research Institute