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Study identifier: NCT06321341 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Efficacy and Safety of Vespireit, Prolonged-release Tablets, in Patients With Autonomic Dysfunction Syndrome Accompanied by Functional Vertigo

Condition: Vertigo · Autonomic Dysfunction  ·  Sponsor: Valenta Pharm JSC

PhasePhase 4
Planned participants160
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

This study aims to evaluate the efficacy and safety of Vespireit, prolonged-release tablets, 15 mg (Valenta Pharm JSC, Russia) in comparison with Arlevert, tablets, 40 mg + 20 mg (Menarini International Operations Luxembourg S.A., Luxembourg) in patients with autonomic dysfunction syndrome accompanied by functional vertigo.

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

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Contact details are listed per location below or on the registry record.

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Locations (4)

Central Clinic LLCBryansk, RussiaRecruiting
Federal State Budgetary Educational Institution of Higher Education "Kirov State Medical University" of the Ministry of Healthcare of the Russian FederationKirov, RussiaRecruiting
State Budgetary Institution of Healthcare of the City of Moscow "V.P. Demikhov City Clinical Hospital of the Department of Healthcare of the City of Moscow"Moscow, RussiaRecruiting
Private Healthcare Institution "Clinical Hospital "RZD-Medicine" of the city of Smolensk"Smolensk, RussiaRecruiting

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Source record: clinicaltrials.gov/study/NCT06321341