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Completed Not applicable Interventional Results available

Dual Field PEMF Therapy in Lower Extremity Painful Diabetic Distal Symmetric Peripheral Neuropathy

ClinicalTrials.gov ID: NCT03455543

Public ClinicalTrials.gov record NCT03455543. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 6, 2026, 2:08 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multi-Center, Double-Blind, Sham-Controlled, Randomized Trial of Dual Field PEMF Therapy [Provant® Therapy System] in Lower Extremity Painful Diabetic Distal Symmetric Peripheral Neuropathy (DSPN) (The RELIEF Trial)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Part A of this trial is a multi-center, prospective, double-blinded, sham-controlled, randomized clinical trial. Part A will evaluate PEMF treatment compared to sham treatment in patients with painful diabetic distal symmetric peripheral neuropathy (DSPN) when treatment is administered 30 minutes twice daily through a 120-day period (4 months). Part B is a 8-month open-label active treatment extension period designed to collect longer-term data on pain, medication use, quality of life and safety (Part B).Part B of this trial is a an extension period upon completion of Part A.

Study identification

NCT ID
NCT03455543
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Regenesis Biomedical, Inc.
Industry
Enrollment
182 participants

Conditions and interventions

Eligibility (public fields only)

Age range
22 Years to 80 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 25, 2018
Primary completion
Nov 13, 2018
Completion
Jul 17, 2019
Last update posted
Jul 14, 2020

2018 – 2019

United States locations

U.S. sites
18
U.S. states
12
U.S. cities
18
Facility City State ZIP Site status
Physician's Research Group Mesa Arizona 85206
Valley Clinical Research Northridge California 91325
Northern California Research Sacramento California 95821
Diabetes Research Center Tustin California 92780
Mountain View Clinical Research Denver Colorado 80209
Lake Internal Medicine Associates Eustis Florida 32726
Clinical Physiology Associates Fort Myers Florida 33912
Spotlight Research Center Miami Florida 33176
Clinical Research of Central Florida Winter Haven Florida 33880
River Birch Research Alliance, LLC Blue Ridge Georgia 30514
MediSphere Medical Research Center, LLC Evansville Indiana 47714
Heartland Research Associate, LLC Wichita Kansas 67207
Healthcare Research Network Hazelwood Missouri 63042
The Center for Pharmaceutical Research, LLC Kansas City Missouri 64114
Palm Research Center Las Vegas Nevada 89128
Great Lakes Medical Resarch Westfield New York 14787
Wake Family Medicine, PC Cary North Carolina 27513
Rainier Clinical Research Renton Washington 98057

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03455543, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 14, 2020 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03455543 live on ClinicalTrials.gov.

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