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Clinical Trial Summary

This study aims to determine safety and feasibility of non-invasive transcutaneous cervical Vagus nerve stimulation (nVNS) when delivered promptly after clinical diagnosis of acute stroke. Vagus nerve stimulation will be performed via GammaCore® device. A total of 60 patients will be randomized to each of 3 different groups; 'standard dose' vagal stimulation, 'high dose' vagal stimulation, and 'sham stimulation' (1:1:1 ratio). Adverse device events, serious adverse device events, and feasibility of vagal nerve stimulation at the setting of acute stroke will be evaluated. The study will be performed in a multi-center fashion among stroke centers within TurkStrokeNet Network.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03733431
Study type Interventional
Source Turkish Stroke Research and Clinical Trials Network
Contact
Status Completed
Phase N/A
Start date May 10, 2019
Completion date April 1, 2021

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