Dexmedetomidinine in the Prevention of Postoperative Delirium in the Intensive Care Unit After Cardiac Surgery

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Novi Sad

About this trial

This is a prospective, randomized, single blinded, controlled clinical trial designed to compare the clinical effects of sedation with dexmedetomidine versus propofol in patients undergoing cardiac surgery.

Eligibility criteria

Qualifiers

patients undergoing open heart surgery with the use of cardiopulmonary bypass (including coronary artery bypass grafting, valve repair/replacement, and combined)

left ventricular ejection fraction (LVEF) >40%.

Disqualifiers

preoperative atrial fibrillation

previous history of interventionally treated arrhythmias

second and third degree atrioventricular block

bradycardia with heart rate ≤50/min

Trial design

Treatments tested in this trial

  • Dexmedetomidine
  • Propofol

Treatment groups

200 Participants
are divided into 2 treatment groups

Sponsors and collaborators