Clinical Trials Directory

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UnknownNCT05004545

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

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.

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
126 (estimated)
Sponsor
Chaudhry Pervaiz Elahi Institute of Cardiology · Other Government
Sex
All
Age
20 Years – 60 Years
Healthy volunteers
Not accepted

Summary

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

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGPropofolPropofol infusion according to body weight will be compared with sevoflurane acording to MAC % to see the lactate level and hemodynamic parameters of CABG patients

Timeline

Start date
2017-06-10
Primary completion
2021-09-20
Completion
2021-12-30
First posted
2021-08-13
Last updated
2021-08-13

Locations

1 site across 1 country: Pakistan

Source: ClinicalTrials.gov record NCT05004545. Inclusion in this directory is not an endorsement.