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NCT06499220 · ClinicalTrials.gov registry record · NA

Electrically Evoked Compound Action Potentials Human Observation Medtronic System Study (ECHO-MDT)

A NA study of Chronic Pain, sponsored by MedtronicNeuro.

Completed
Registry status
NA
Development phase
201
Enrollment target
10
Study locations

NCT06499220 is a NA study of Chronic Pain that has completed, run by MedtronicNeuro. The registered enrollment target is 201 participants, below the 772-participant average among 301 other Chronic Pain trials with a reported enrollment target (74% lower). The trial reports 10 study locations across 6 states.

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The verdict

NCT06499220, a NA study of Chronic Pain, has completed, sponsored by MedtronicNeuro.

COMPLETED
Registry status
NA
Development phase
201 participants
Enrollment target
10
Study locations

Study Summary

This is a prospective, multi-center, non-significant risk IDE study of evoked waveforms resulting from stimulation of the dorsal column using a closed-loop system. comprised of Medtronic hardware or off the shelf hardware, which uses recorded waveforms to adjust stimulation amplitude.

Conditions Studied

Interventions

  • DEVICE Spinal Cord Stimulator

Study Locations (10)

Minnesota

  • Nura Research Institute - Edina
  • Twin Cities Pain Clinic - Edina
  • iSpine Pain Physicians - Maple Grove

Ohio

  • The Ohio State University Wexner Medical Center - Columbus
  • Kettering Health - Kettering
  • Premier Pain Treatment Institute - Mount Orab

California

  • Coastal Pain and Spinal Diagnostics - Carlsbad

Iowa

  • MercyOne Des Moines Medical Center - Des Moines

Pennsylvania

  • Center for Interventional Pain and Spine - Lancaster

West Virginia

  • Rockefeller Neuroscience Institute West Virginia University - Morgantown

Trial Details

FieldValue
Enrollment Target 201 participants
Start Date 2019-10-30
Est. Completion 2023-10-16
Phase NA

Sponsor

MedtronicNeuro

51 total trials

What the Registry Record Tells You About NCT06499220

The ClinicalTrials.gov registry entry for NCT06499220 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 201 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 772-participant average among 301 other Chronic Pain trials with a reported enrollment target (74% lower). The listed sponsor is MedtronicNeuro, which has 51 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Chronic Pain appearing as the primary indexed condition, and to 1 intervention - of which Spinal Cord Stimulator is the first listed.

NCT06499220 reports 10 study locations spanning 6 distinct geographic areas - top geographies include Minnesota, Ohio, California.

Frequently Asked Questions

What is clinical trial NCT06499220 about?

NCT06499220 is a clinical study titled "Electrically Evoked Compound Action Potentials Human Observation Medtronic System Study (ECHO-MDT)". This is a prospective, multi-center, non-significant risk IDE study of evoked waveforms resulting from stimulation of the dorsal column using a closed-loop system. comprised of Medtronic hardware or off the shelf hardware, which uses recorded waveforms to adjust stimulation amplitude.

What is the current status of trial NCT06499220?

This trial is currently completed. It is a NA study. The enrollment target is 201 participants. The study started on 2019-10-30. Estimated completion is 2023-10-16.

What conditions does trial NCT06499220 study?

This clinical trial studies the following conditions: Chronic Pain.

What interventions are being tested in trial NCT06499220?

The interventions under investigation include: Spinal Cord Stimulator (DEVICE).

Who is sponsoring clinical trial NCT06499220?

This trial is sponsored by MedtronicNeuro, which has 51 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06499220 being conducted?

This trial has 10 study locations across California, Iowa, Minnesota, Ohio, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.