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Clinical Trial Summary

Trial title: A Randomized, Double Blind Sham Controlled Clinical Trial to Evaluate the Efficacy of Electrical Vestibular Nerve Stimulation (VeNS), Compared to a Sham Control for Treatment of PTSD The aim of this study: To better evaluate the efficacy of non-invasive electrical vestibular nerve stimulation (VeNS) as a method of treating PTSD, as compared to a sham control. Allocation: Randomized to either active device or control device usage. Endpoint classification: Efficacy Study Intervention Model: Parallel Assignment in 1:1 active to control allocation Sample size: The aim is to recruit a total of up to 300 participants. The study will last 12 weeks in total for each subject.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05242367
Study type Interventional
Source Neurovalens Ltd.
Contact Joe Reel
Phone 2890991835
Email joe.reel@neurovalens.com
Status Recruiting
Phase N/A
Start date February 13, 2023
Completion date October 2024

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