ReActiv8 Implantable Neurostimulation System for Chronic Low Back Pain
Public ClinicalTrials.gov record NCT02577354. 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.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
ReActiv8 Implantable Neurostimulation System for Chronic Low Back Pain (ReActiv8-B)
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
The purpose of this trial is to evaluate the safety and efficacy of ReActiv8 for the treatment of adults with Chronic Low Back Pain when used in conjunction with medical management.
Study identification
- NCT ID
- NCT02577354
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Not applicable
- Enrollment
- 204 participants
Conditions and interventions
Conditions
Interventions
- ReActiv8 Implantable Stimulation System (Patient Appropriate Stimulation) Device
- ReActiv8 Implantable Stimulation System (Low Stimulation) Device
Device
Eligibility (public fields only)
- Age range
- 22 Years to 75 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
- Jul 31, 2016
- Primary completion
- Oct 31, 2018
- Completion
- Dec 31, 2023
- Last update posted
- Feb 26, 2025
2016 – 2024
United States locations
- U.S. sites
- 16
- U.S. states
- 12
- U.S. cities
- 15
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| University of California, San Diego | La Jolla | California | — | — |
| The Spine Institute | Santa Monica | California | — | — |
| University of Colorado Hospital | Aurora | Colorado | — | — |
| Indiana Spine Group | Carmel | Indiana | — | — |
| OrthoIndy | Indianapolis | Indiana | — | — |
| University of Kansas Medical Center | Kansas City | Kansas | — | — |
| The Brigham and Women's Hospital | Boston | Massachusetts | — | — |
| Beaumont Health | Royal Oak | Michigan | — | — |
| Duke University Medical Center | Durham | North Carolina | — | — |
| Center for Clinical Research | Winston-Salem | North Carolina | — | — |
| Louis Stokes VA Medical Center | Cleveland | Ohio | — | — |
| University Hospitals Cleveland Medical Center | Cleveland | Ohio | — | — |
| Rhode Island Hospital | Providence | Rhode Island | — | — |
| Upstate Clinical Trials | Spartanburg | South Carolina | — | — |
| Northwest Orthopaedic Specialists | Spokane | Washington | — | — |
| Center for Pain Relief | Charleston | West Virginia | — | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
Non-U.S. locations
This page focuses on the U.S. directory. The official record also lists 10 non-U.S. sites.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT02577354, 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 Feb 26, 2025 · Synced Sep 5, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT02577354 live on ClinicalTrials.gov.