ClinicalTrials.gov record
Terminated Not applicable Interventional Results available

Subcutaneous Nerve Stimulation for Failed Back Surgery Syndrome (FBSS) Patients

ClinicalTrials.gov ID: NCT01818297

Public ClinicalTrials.gov record NCT01818297. 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 May 17, 2026, 4:41 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

SubQStim Pivotal Study: A Prospective, Randomized, Controlled Study to Evaluate the Safety and Efficacy of Subcutaneous Nerve Stimulation. Protocol 1666

Study identification

NCT ID
NCT01818297
Recruitment status
Terminated
Study type
Interventional
Phase
Not applicable
Lead sponsor
MedtronicNeuro
Industry
Enrollment
137 participants

Conditions and interventions

Interventions

  • PrimeAdvanced® neurostimulator system Device

Device

Eligibility (public fields only)

Age range
22 Years and older
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 31, 2013
Primary completion
Feb 29, 2016
Completion
Feb 29, 2016
Last update posted
Sep 20, 2017

2013 – 2016

United States locations

U.S. sites
27
U.S. states
16
U.S. cities
25
Facility City State ZIP Site status
Valley Pain Consultants Phoenix Arizona 85001
HOPE Research Institute Phoenix Arizona 85018
Coastal Pain Research Carlsbad California 92009
Pain Medicine Associates Fountain Valley California 92708
Florida Pain Institute Merritt Island Florida 32953
Advanced Medicine and Pain Management Research Miami Florida 33145
Compass Research, LLC Orlando Florida 32806
Emory University School of Medicine Atlanta Georgia 30322
Rush University Medical Center Chicago Illinois 60612
University of Illinois at Chicago Chicago Illinois 60612
University of Kansas Medical Center Kansas City Kansas 66160
Willis Knighton River Cities Clinical Research Center Shreveport Louisiana 71105
Comprehensive Pain and Rehabilitation Pascagoula Mississippi 39581
Columbia Interventional Pain Center, LLP Columbia Missouri 65201
Mercy Medical Research Institute Springfield Missouri 65804
NYU Langone Medical Center New York New York 10016
Mayfield Clinic Cincinnati Ohio 45219
University Hospitals Case Medical Center Cleveland Ohio 44106
Ohio State University Columbus Ohio 43210
Summa Western Reserve Hospital Cuyahoga Falls Ohio 44223
DNA Advanced Pain Treatment Center Greensburg Pennsylvania 15601
Thomas Jefferson University Philadelphia Pennsylvania 19107
Southern Spine Institute Mt. Pleasant South Carolina 29464
Austin Pain Associates Cedar Park Texas 78613
Space City Pain Specialists Webster Texas 77598
Lifetree Clinical Research Salt Lake City Utah 84106
Wisconsin Health Center Surgery Center Greenfield Wisconsin 53220

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 NCT01818297, 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 Sep 20, 2017 · Synced May 17, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01818297 live on ClinicalTrials.gov.

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