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RECRUITING
NCT04427241
PHASE4

Efficacy and Safety of Cerebrolysin on Prolonged Disorders of Consciousness

Sponsor: Konkuk University Medical Center

View on ClinicalTrials.gov

Summary

Object: To determine the effect of cerebrolysin on prolonged disorders of consciousness caused by hemorrhagic stroke. Participants: patients with prolonged disorders of consciousness due to severe traumatic brain injury Intervention: 30 ml cerebrolysin + 70 ml normal saline, days 4-17, once/day, intravenously or 100 ml normal saline, days 4-17, once/day, IV Comparison: cerebrolysin group versus control group Outcome: Coma Recovery Scale-revised, FDG-PET signal

Official title: Efficacy and Safety of Cerebrolysin on Prolonged Disorders of Consciousness in Patients With Hemorrhagic Stroke: A Pilot Study

Key Details

Gender

All

Age Range

19 Years - 120 Years

Study Type

INTERVENTIONAL

Enrollment

12

Start Date

2023-06-01

Completion Date

2026-12-31

Last Updated

2026-05-11

Healthy Volunteers

No

Interventions

DRUG

Cerebrolysin

30 ml cerebrolysin + 70 ml normal saline, days 4-17, once/day, intravenously

DRUG

Control

100 ml normal saline, days 4-17, once/day, IV

Locations (1)

Konkuk University Medical Center Research Coordinating Center

Seoul, South Korea