None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patient should be of age 18-60 yrs. Patient to get fit under ASA PS I and II Patient should undergo Elective non cardiac surgery under General Anesthesia
Exclusion criteria
Exclusion criteria: Patient who refused to give consent for study. Patient with known hypersensitivity to these study drugs. Baseline Heart rate less than 60 Baseline systolic Bp less than 100. Those with ECG abnormalities. Patients with history of chest pain/palpitations/syncope, Patients with history of any visual disturbances, with Sick sinus syndrome. Patients already on calcium channel blockers, azole antifungals, antiretroviral drugs and macrolide antibiotics, with hepatic impairment or renal dysfunction, pregnant and breastfeeding females and 9. Patients in whom intubation is thought to be difficult (time taken to intubate >
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To the best of literature . There is no study evaluating the hemodynamic attenuation of laryngoscope and endotracheal intubation comparing oral ivabradine & oral clonidine & with the previous studies & previous records .however studies have done between clonidine vs gabapentin & ivabradine alone. Timepoint: Laryngoscopic response till 5 minutes | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. To the study the effect of these drugs on hemodynamic during intra operative & post operative Period . 2. To study about the side effects & complications such as visual disturbances , arrhythmias, etc , if any due to the study drugs. Timepoint: At baseline ,1 hr , 2hrs , 3hrs , one week | — |
Countries
India
Contacts
Sri Manakula Vinayagar Medical College and Hospital