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Intraoperative Dexmedetomidine and Coronary Artery Bypass Graft Surgery
NOT_RECRUITINGPhase 2/3Sponsored by University of Novi Sad
No longer actively recruiting
PhasePhase 2/3
SponsorUniversity of Novi Sad
Started2024-04-03
Est. completion2024-07
Eligibility
Age18 Years+
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT06378827
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.
Eligibility
Age: 18 Years+Healthy volunteers accepted
Inclusion Criteria: * Elective coronary artery bypass graft surgery * Age over 18 years * ASA score 3 or 4 * Voluntary consent of the patient to participate in the research Exclusion Criteria: * Emergency coronary artery bypass graft surgery * Chronic renal failure with eGFR \<60 ml/min/1.73m2 * Left ventricular ejection fraction \<30% * 2nd or 3rd degree atrioventricular block * Use of nephrotoxic agents such as aminoglycoside antibiotics or contrast agents within the last 48 hours * Previous heart surgery or kidney surgery * Allergy to dexmedetomidine
Conditions2
Acute Kidney InjuryHeart Disease
Interventions1
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No longer actively recruiting
PhasePhase 2/3
SponsorUniversity of Novi Sad
Started2024-04-03
Est. completion2024-07
Eligibility
Age18 Years+
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT06378827