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Study identifier: NCT07575984 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Mexidol® Safety and Efficacy in Treatment of Hyperacute and Acute Ischemic Stroke

Condition: Ischemic Stroke  ·  Sponsor: Pharmasoft

PhasePhase 4
Planned participants120
Who can joinAll sexes, 18 Years to 90 Years
Healthy volunteersYes

About this study

The primary objective of this study is to further define the mechanisms of action of Mexidol® (solution for intravenous and intramuscular injection, 50 mg/ml) and Mexidol® FORTE 250 (film-coated tablets, 250 mg) in the hyperacute and acute periods of ischemic stroke, and to evaluate their impact on clinical and neuroimaging outcomes of the disease.

This description comes directly from the study's public registry record.

Talk to the study team

Yuriy E. Meshcherskiy, Medical Director, LLC "RPC "PHARMASOFT", Medical Director  ·  007 (495) 626-47-55  ·  pharmasoft@pharmasoft.ru

Always discuss trial participation with your own doctor first.

Locations (9)

First City Clinical Hospital named after E.E. VolosevichArkhangelsk, RussiaRecruiting
Ivanovo Regional Clinical HospitalIvanovo, RussiaRecruiting
Regional Clinical HospitalRyazan, RussiaRecruiting
Hospital for War VeteransSaint Petersburg, RussiaRecruiting
City Hospital № 40 of Kurortny DistrictSaint Petersburg, RussiaRecruiting
Smolensk Regional Clinical HospitalSmolensk, RussiaRecruiting
Regional Clinical HospitalTver', RussiaRecruiting
Regional Clinical HospitalYaroslavl, RussiaRecruiting
Zhukovskiy Regional Clinical Hospital,Zhukovskiy, RussiaRecruiting

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Source record: clinicaltrials.gov/study/NCT07575984