Perioperative pain. Other specified complications of cardiac and vascular prosthetic devices, implants and grafts
Conditions
Interventions
Intervention 1: In paracetamol group 15 minutes before induction of anesthesia 1 g intravenous paracetamol in 50 cc normal saline solution was infused to the patient within 15 minutes.
Next dose of p
Prevention
In paracetamol group 15 minutes before induction of anesthesia 1 g intravenous paracetamol in 50 cc normal saline solution was infused to the patient within 15 minutes.
Next dose of paracetamol was
In the control group at all stages of paracetamol injection instead of paracetamol equal volume of normal saline was used.
Sponsors
Isfahan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
40 Years to 70 Years
Inclusion criteria
Inclusion criteria: Inclusion Criteria: Inclusion criteria for the study were: undergoing elective surgery CABG, the individual agreement to participate in the study, age 40 to 70 years, not having liver failure (Serum bilirubin greater than 1.8 mg per deciliter and aspartate and alanine aminotransfraz more than 1.5 times of the upper limit of normal), not having renal failure (serum creatinine greater than 2 mg per deciliter), not addictive to opioid drugs and psychotropic substances, and having cardiac ejection fraction greater than 30%., Exclusion criteria for the study: Excessive bleeding after surgery (more than 150 ml for the first two hours), having other surgeries in addition to coronary artery bypass surgery such as repair or replacement of heart valves, repeated surgery, and the need for aortic balloon support.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: during study. Method of measurement: VAS and FAS. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMojtaba Mansouri
Isfahan Univrsity of Medical Sciences
Outcome results
None listed