500
Participants
Start Date
January 1, 2024
Primary Completion Date
June 30, 2025
Study Completion Date
December 31, 2025
Cerebrolysin
Patients were randomized into two groups: CBL - patients treated with cerebrolysin at the daily dose of 50 mL, and K - control patients treated without cerebrolysin. Cerebrolysin was administrated intravenously on the day the delirium was detected and then for seven consecutive days.
Saline Solution - IV
Patients enrolled in group K received the infusion of 0.9% Saline solution at a volume of 250 mL.
First Department of Anaesthesiology and Intensive Therapy Medical University of Lublin, Lubin
Medical University of Lublin
OTHER