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Intraoperative Dexmedetomidine and Coronary Artery Bypass Graft Surgery
Sponsor: University of Novi Sad
Summary
This is a prospective randomized clinical trial designed to determine the effect of intraoperative dexmedetomidine administration on renal function after coronary artery bypass graft surgery.
Official title: The Effect of Intraoperative Dexmedetomidine on Renal Function After Coronary Artery Bypass Graft Surgery
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
100
Start Date
2024-04-03
Completion Date
2024-10
Last Updated
2024-04-23
Healthy Volunteers
No
Conditions
Interventions
Dexmedetomidine
Dexmedetomidine solution will be prepared by diluting one ampoule of dexmedetomidine (200µg/2ml) with 48 ml of saline solution to obtain a dexmedetomidine solution of 4µg/ml. Patients from the experimental group will receive a continuous infusion of dexmedetomidine at a dose of 0.5 µg/kg/h, until the end of the operation.
Locations (1)
University of Novi Sad, Faculty of Medicine
Novi Sad, Serbia