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Clinical Trial 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


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04427241
Study type Interventional
Source Konkuk University Medical Center
Contact
Status Not yet recruiting
Phase Phase 4
Start date June 1, 2023
Completion date December 31, 2025

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