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Clinical Trial Summary

This is a prospective, single center, interventional clinical study containing two cohorts the treatment cohort and control cohort. A total of 13 subjects will be enrolled. Three (3) healthy volunteers will be enrolled in the control cohort and undergo imaging only. Ten (10) subjects who have recently experienced a mild to moderate acute ischemic stroke will receive treatment using the NeuroGlove.


Clinical Trial Description

This is a prospective, single center, interventional clinical study containing two cohorts the treatment cohort and control cohort. A total of 13 subjects will be enrolled. Three (3) healthy volunteers will be enrolled in the control cohort and undergo imaging only. Ten (10) subjects who have recently experienced a mild to moderate acute ischemic stroke will receive treatment using the NeuroGlove. Up to 13 subjects enrolled and complete study procedures. There will be 2 cohorts enrolled in the study: 1. Control Cohort: 3 healthy volunteers 2. Treatment Cohort: 10 subjects who have experienced mild to moderate stroke symptoms* that did not completely resolve after acute interventions. - Mild to moderate stroke symptoms is defined as a NIHSSS score of 3 to 15. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05961293
Study type Interventional
Source NeuroGlove LLC
Contact Thomas Harold
Phone 612.255.0405
Email tharold@neuroglove.net
Status Not yet recruiting
Phase N/A
Start date December 1, 2023
Completion date November 1, 2024

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