None listed
Conditions
Brief summary
The primary purpose of this study is to compare the analgesic effect of lidocaine in reducing intensity of pain in patient undergoing cardiac surgery, for coronary artery bypass graft . The comparison was done with two other analgesics, acetaminophen and morphine , as a control treatment for reducing intensity of pain in patient undergoing cardiac surgery, for coronary artery bypass graft . Intravenous administration of lidocaine provides a more satisfactory postoperative analgesia compared to the application of morphine and acetaminophen in the postoperative period
Interventions
Post operative pain management after cardiac surgery.
The goal of the intervention is to reduce the intensity of pain.
Two groups are included in the study as control treatment, each group has 20 patients
Group 1(A) has received acetaminophen intravenous 1gr every 4 hour, for 48 hours post operative, starting immediately upon termination of anesthesia
Group 2 (M) received morphine intravenous 5mg every 6 hours, for 48 hours post operative, starting immediately upon termination of anesthesia
Sponsors
University Clinical Center of Kosovo
Study design
Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
All the patient planed for elective cardiopulmonary bypass surgery, ASA classification (American Society of Anesthesiologists ) II-IV
Exclusion criteria
patient rejection, unconscious patients, patients taking chronically opioids patient with renal insufficiency gr III-IV, hepatic insufficiency gr III-IV, psychiatric patients, patients allergy in acetaminophen, morphine or lidocaine respectively
Outcome results
None listed