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Clinical Trial Summary

The purpose of this study is to evaluate the effectiveness and safety of SCONE neuromodulation therapy after 12 weeks of therapy in comparison to inactive sham control in improving symptoms of Neurogenic Lower Urinary Tract Dysfunction


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05301335
Study type Interventional
Source SpineX Inc.
Contact Parag Gad
Phone 4082035061
Email info@spinex.co
Status Recruiting
Phase N/A
Start date May 25, 2022
Completion date April 1, 2024

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