Coronary artery bypass grafting. Presence of aortocoronary bypass graft
Conditions
Interventions
Intervention 1: Intervention group: inflation of the blood pressure cuff for 5 minutes and deflation for 5 minutes with 4 repeats. Intervention 2: Control group: no intervention.
Sponsors
Tehran University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Candidate for coronary artery bypass grafting with cardiopulmonary bypass Normal upper limb examinations Not having surgical operations in the past three months Not having acute medical conditions during the last three months
Exclusion criteria
Exclusion criteria: Known inflammatory disorders Diabetes Liver disease Kidney disease Receiving vitamins C and/or E and/or other antioxidants
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Total antioxidant capacity. Timepoint: After anesthesia induction, after cardiopulmonary bypass, 24 hours after intensive care unit admission. Method of measurement: With turbidimetry analysis.;Glutathione peroxidase activity assay. Timepoint: After anesthesia induction, after cardiopulmonary bypass, 24 hours after intensive care unit admission. Method of measurement: With turbidimetry analysis. | — |
Secondary
| Measure | Time frame |
|---|---|
| Troponin level. Timepoint: After anesthesia induction, after cardiopulmonary bypass, 24 hours after intensive care unit admission. Method of measurement: ELISA.;Ejection fraction. Timepoint: Every 8 hours after intensive care unit admission. Method of measurement: Echocardiography. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFarhad Gorjipour
Shahid Beheshti University of Medical Sciences
Outcome results
None listed