Coronary artery bypass graft.
Conditions
Interventions
Intervention 1: Intervention group: Intervention group: Paracetamol 10mg / kg diluted in 100 ml of normal saline for 30 minutes every 6 hours up to 24 hours. Intervention 2: Intervention group: and in
Sponsors
Ahvaz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
30 Years to 70 Years
Inclusion criteria
Inclusion criteria: Age between 30 and 70 years Candidate for coronary artery bypass graft
Exclusion criteria
Exclusion criteria: Gastrointestinal Disease Kidney disease Liver disease EF<30% Off pump surgery
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative pain control. Timepoint: 0, 6, 12 and 24 hours after extubation. Method of measurement: VAS.;Arterial oxygen saturation drop. Timepoint: 0, 6, 12 and 24 hours after extubation. Method of measurement: Yes or no.;Blood pressure changes. Timepoint: 0, 6, 12 and 24 hours after extubation. Method of measurement: Three groups: mild to moderate.;Chest tube discharge. Timepoint: 0, 6, 12 and 24 hours after extubation. Method of measurement: The volume of discharge. | — |
Secondary
| Measure | Time frame |
|---|---|
| Arrhythmia. Timepoint: 0, 6, 12 and 24 hours after exteubation. Method of measurement: monitoring.;Duration of ventilator dependence. Timepoint: 0, 6, 12 and 24 hours after exteubation. Method of measurement: Duration of respiratory support. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFatemeh Javaherforoosh zadeh
Ahvaz University of Medical Sciences
Outcome results
None listed