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Clinical trialNCT05972889CompletedInterventional

Randomized Blinded Evaluation of the Effects of TENS and IFC Compared to a Sham Device and SOC in Patients With Non-Specific CLBP

SponsorZynex Medical, Inc.Enrollment334Non-Specific Chronic Lower Back Pain
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

This is a prospective, sham-controlled, randomized, single-blinded, multi-center study comparing two different modes of the NexWave device, transcutaneous electrical nerve stimulation (TENS) and interferential current (IFC), with an identical non-functioning NexWave sham device or self-defined standard of care for improvement of pain intensity of non-specific CLBP.
clinicaltrials.gov ↗

Investigators

The overall officials registered on this study. Names that resolve to a FindMyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

8 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Dbps Research

    Greenwood Village, Colorado, United States

  • Mcgreevy Neurohealth

    Saint Augustine, Florida, United States

  • Peachtree Orthopedics

    Atlanta, Georgia, United States

  • Horizon Clinical Research

    Jasper, Georgia, United States

  • Applied Pain Institute, Llc

    Bloomington, Illinois, United States

  • One Oak Medical

    Congers, New York, United States

  • the Center for Clinical Research, Llc

    Winston-Salem, North Carolina, United States

  • Summit Brain, Spine and Orthopedics

    Lehi, Utah, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
2 Nov 2023
Primary completion
21 Oct 2025
Completion
21 Oct 2025
Last update posted
28 Oct 2025
Registered enrollment
334
Registry id
NCT05972889
clinicaltrials.gov ↗

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 4 Nov 2026. Registry facts are shown as registered by the study sponsor; FindMyKOL does not interpret them.