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

Recruiting N/A Interventional Study
Neuropathy Neuropathy;Peripheral
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
22 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
32 (estimated)
Sponsor
Erchonia Corporation · Industry
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About This Trial

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.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Previously diagnosed with idiopathic peripheral neuropathy by a suitably qualified and licensed health professional within the past 6 months. * Over the age of 22 years of age * Able to read and write English * Constant feet pain on-going over at least the past 3 months * Subj…
Contacts

Travis Sammons

8882420571

tsammons@erchonia.com

CONTACT