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Clinical Trial Summary

This double blind randomized controlled study will enroll 20 subjects and will be conducted remotely. The study will be randomized for an 8-week period with a 1:1 active to sham device allocation. Primary endpoint analysis will be performed at 4 weeks.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04780893
Study type Interventional
Source Neurovalens Ltd.
Contact
Status Withdrawn
Phase N/A
Start date February 1, 2022
Completion date April 2022

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