respiratory and cerebral outcomes. Respiratory failure, unspecified with hypercapnia, Sedative, hypnotic or anxiolytic use, unspecified with sedative, hypnotic or anxiolytic-induced sleep disorder
Conditions
Interventions
Intervention 1: Intervention Group: After induction of anesthesia and endotracheal intubation, surgery will begin and after isolation of the patient from cardiopulmonary pump, modafinil (the drug is p
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: patients with coronary artery bypass graft surgery patients with a cardiac ejection fraction of more than 40%
Exclusion criteria
Exclusion criteria: Patients with hepatic function failure Patients with renal function failure Patients with irregular cardiac primary rhythms Patients with cardiomegaly patients who have drug addiction patients who have alcoholism patients who are using psychiatric drugs
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The time to reach full consciousness. Timepoint: Every hour until you reach full consciousness. Method of measurement: Richmond-Agitation Scale.;Duration of mechanical ventilation in the intensive care unit. Timepoint: Every hour until you reach full consciousness. Method of measurement: In minutes using time meter.;Length of stay in Intensive Care Unit. Timepoint: Every day until discharge from Intensive Care Unit. Method of measurement: By day using Count days.;Carbon dioxide arterial pressure. Timepoint: Every one hour. Method of measurement: Arterial blood samples based on mercury mm. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Mojtaba Mansouri
Esfahan University of Medical Sciences
Outcome results
None listed