Cerebrolysin in Critically Ill Patients With Delirium

NAEnrolling by invitationINTERVENTIONAL
Enrollment

500

Participants

Timeline

Start Date

January 1, 2024

Primary Completion Date

June 30, 2025

Study Completion Date

December 31, 2025

Conditions
Cognitive Impairment
Interventions
DRUG

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.

OTHER

Saline Solution - IV

Patients enrolled in group K received the infusion of 0.9% Saline solution at a volume of 250 mL.

Trial Locations (1)

20-090

First Department of Anaesthesiology and Intensive Therapy Medical University of Lublin, Lubin

All Listed Sponsors
lead

Medical University of Lublin

OTHER