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Compare Hemodynamic Parameters of Propofol and Sevoflurane During CPB Time in Undergoing CABG to Avoid Lactate Level

Hemodynamic Instability Clinical Trial

Official title:
To Compare Hemodynamic Parameters of Propofol and Sevoflurane During Cardiopulmonary Bypass Time in Patients Undergoing Coronary Artery Bypass Graft (CABG) Surgery to Avoid Lactate Level.

Clinical Trial Summary

Hemodynamic parameters and lactate level will be on CBP during CABG surgery patients.

Clinical Trial Description

Objective: To compare hemodynamic parameters of propofol and sevoflurane during cardiopulmonary bypass time in patients undergoing coronary artery bypass graft (CABG) surgery to avoid lactate level. Methods: One hundred and twenty six patients scheduled for CABG from May 2017 to May 2018 will be included in this study. Non probability consecutive sampling will be used. Patients will be divided in two groups, propofol will be given to group 1, and sevoflurane will be given to group 2. Age, clamp time, bypass time, mean arterial blood pressure on bypass machine and lactate level will be compared between two groups. SPSS version 24 will used and p value ≤ 0.05 will be considered as significant. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05004545
Study type Interventional
Source Chaudhry Pervaiz Elahi Institute of Cardiology
Contact Kaneez Ume Farwa, FCPS
Phone +923356787214
Email farwatirmizi@hotmail.com
Status Recruiting
Phase N/A
Start date June 10, 2017
Completion date December 30, 2021
View Details
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