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Clinical Trial Summary

The purpose of this single-center, prospective, randomized, double-blind, sham controlled, parallel-group study is to collect clinical data related to the safety and efficacy of vagus nerve stimulation for the acute and preventive treatment of Post Traumatic Headache.


Clinical Trial Description

The study will enroll 60 subjects over a period of 14 weeks each. Subjects will use either a sham or active device to treat acute Post Traumatic Headache. Investigators will collect clinical data related to the use of the device. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04071743
Study type Interventional
Source University of Texas Southwestern Medical Center
Contact
Status Withdrawn
Phase N/A
Start date January 1, 2020
Completion date December 31, 2021

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