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Clinical Trial Summary

Evaluation of the efficacy and safety of Cytoflavin®, solution for intravenous administration, (OOO NTFF POLYSAN, Russia) for 10 days, patients with cerebral infarction who receive reperfusion therapy, with the start of treatment within the first 24 hours from the stroke onset, compared to treament with any other neuroprotective drug which may be used in routine clinical practice.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05297851
Study type Observational
Source POLYSAN Scientific & Technological Pharmaceutical Company
Contact
Status Completed
Phase
Start date April 10, 2022
Completion date March 1, 2023

See also
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