Cytoflavin in Combination With Reperfusion in Stroke Patients

Status Completed

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

Clinical Trial Details

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

View Details

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