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Clinical Trial Summary

The Etude Study is a multi-center, four-arm prospective dose-adjusting study designed to assess the tolerability, safety and efficacy of non-invasive sensory stimulation for patients with cognitive impairment.


Clinical Trial Description

Subjects will be enrolled in two Cohorts (N=10 each, enrolled sequentially), and each will assess two different dose levels (randomly assigned). Based on initial outcomes in Cohort 1 at Interim Analysis, the doses for Cohort 2 will be escalated or decreased. Subjects will participate in 1 year (48 weeks) of daily therapy dose using the non-invasive, non-significant risk sensory stimulation medical device. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03661034
Study type Interventional
Source Cognito Therapeutics, Inc.
Contact
Status Active, not recruiting
Phase N/A
Start date May 31, 2018
Completion date March 1, 2022

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