Health Condition 1: I00-I99- Diseases of the circulatory system Health Condition 2: null- patients undergoing cardiac surgeries under cardiopulmonary bypass
Conditions
Interventions
Intervention1: esmolol- lignocaine infusion: esmolol- lignocaine infusion in the test group @ 40 mcg/kg/min during the cross clamp time in CPB
Control Intervention1: normal saline: as a placebo agent
Sponsors
CTVS ICU Advanced Cardiac centre PGIMER
Eligibility
Inclusion criteria
Inclusion criteria: patients with cardiac disease undergoing cardiac surgery under cardio-pulmonary bypass with ejection fraction of <50% for Coronary artery bypass graft surgeries And <60% for Aortic regurgitation and Mitral regurgitation valve repair surgeries .
Exclusion criteria
Exclusion criteria: Patients not willing for the study,with asthma, existing atrial flutter or fibrillation, allergy to esmolol or lignocaine, hepatic or renal dysfunction.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the incidence of arrhythmias after CPB either by using HOLTERS monitor or saved ECG record in the ICU monitor during first 24 hours in patients receiving esmolol-lignocaine infusion on CPB with control group receiving placebo infusion.Timepoint: first 24 hours post CPB. | — |
Secondary
| Measure | Time frame |
|---|---|
| To compare pain score,analgesia requirement, inotropic requirement and mechanical ventilation duration post operatively after CPB separation for first 24 hours.Timepoint: first 24 hours post CPB | — |
Countries
India
Contacts
Public ContactDr Virendra K Arya
PGIMER
Outcome results
None listed