coronary artery bypass.
Conditions
Interventions
Intervention 1: Control group: General anesthesia is administered intravenously with midazolam 2 mg, fentanyl 3 µg/kg, lidocaine (20%) 1.5 mg/kg, thiopental sodium 3 mg/kg and atracurium 0.6 mg/kg. In
Sponsors
Ahvaz University of Medical Sciences
Eligibility
Sex/Gender
Male
Age
40 Years to 65 Years
Inclusion criteria
Inclusion criteria: Male patients who are candidates for coronary artery bypass surgery Age group 40 to 65 years
Exclusion criteria
Exclusion criteria: History of cardiac surgery History of coagulopathy Antiplatelet consumption before surgery Severe lumbar deformity or BMI greater than 35 Contraindication of neuro-axial block Systemic or local infection
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Tidal Volume (TV). Timepoint: 1, 2, 4, 6 and 12 hours after extubation. Method of measurement: Spirometry.;Vital Capacity (VC). Timepoint: 1, 2, 4, 6 and 12 hours after extubation. Method of measurement: The sum of Tidal Volume (TV) and Inspiratory Reserve Volume (I.R.V) and Expiratory Reserve Volume (E.R.V) (Using spirometry).;The partial pressure of carbon dioxide (PaCO2). Timepoint: 1, 2, 4, 6 and 12 hours after extubation. Method of measurement: Blood test.;The partial pressure of oxygen (PaO2). Timepoint: 1, 2, 4, 6 and 12 hours after extubation. Method of measurement: Blood test.;Blood PH. Timepoint: 1, 2, 4, 6 and 12 hours after extubation. Method of measurement: Blood test. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSina Dehdashtiha
Ahvaz University of Medical Sciences
Outcome results
None listed