drugset / Trial / NCT05047952

Vortioxetine for Post-COVID-19 Condition

NCT05047952

Phase 2 Completed 149 enrolled Brain and Cognition Discovery Foundation
RandomizedParallel-groupQuadruple-blindTreatment

Summary

A randomized, double-blinded, placebo-controlled trial will be conducted to evaluate vortioxetine, an antidepressant with established pro-cognitive properties, for the treatment of cognitive deficits which develop during or after an infection consistent with COVID-19, continue for 2+ months, and are not explained by an alternative diagnosis (i.e., post-COVID-19 condition). Participants (aged 18-64 years) will receive vortioxetine (10-20 mg) or placebo for 8 weeks. Participants 65+ years will receive vortioxetine (5-10 mg) or placebo for 8 weeks. Changes in cognitive functioning from baseline to endpoint (week 8) will be assessed via the Digit Symbol Substitution Test (DSST). Study visits may be conducted remotely (e.g. via Zoom, by telephone), and/or in-person.

Timeline

Start
2021-09-16
Primary completion
2023-02-22
Completion
2023-02-22

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Vortioxetine Unknown 10 mg
Subject Vortioxetine Unknown 20 mg