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Study identifier: NCT06912646 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Clinical Efficacy of the Erchonia EVRL for Providing Temporary Relief of Idiopathic Peripheral Neuropathy Foot Pain

Condition: Neuropathy · Neuropathy;Peripheral  ·  Sponsor: Erchonia Corporation

PhaseNA
Planned participants32
Who can joinAll sexes, 22 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of this clinical study is to determine the effectiveness of the Erchonia® EVRL™, manufactured by Erchonia Corporation (the Company), in providing prescription home use application for temporary relief of idiopathic neuropathy foot pain in individuals diagnosed with idiopathic neuropathy by a suitably qualified and licensed health professional.

This description comes directly from the study's public registry record.

Talk to the study team

Travis Sammons  ·  8882420571  ·  tsammons@erchonia.com

Always discuss trial participation with your own doctor first.

Locations (1)

Franco & CoMiramar, Florida, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06912646