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NCT00200122 · ClinicalTrials.gov registry record · Phase 4
Restore Claims Characterization Study
A Phase 4 study of Chronic Refractory Pain Associated With Failed Back Surgery Syndrome, Epidural Fibrosis, Peripheral Causalgia, Complex Regional Pain Syndrome, sponsored by MedtronicNeuro.
- Completed
- Registry status
- Phase 4
- Development phase
- 100
- Enrollment target
- 8
- Study locations
NCT00200122 is a Phase 4 study of Chronic Refractory Pain Associated With Failed Back Surgery Syndrome, Epidural Fibrosis, Peripheral Causalgia, Complex Regional Pain Syndrome that has completed, run by MedtronicNeuro. The registered enrollment target is 100 participants. The trial reports 8 study locations across 7 states.
The verdict
NCT00200122, a Phase 4 study of Chronic Refractory Pain Associated With Failed Back Surgery Syndrome, Epidural Fibrosis, Peripheral Causalgia, Complex Regional Pain Syndrome, has completed, sponsored by MedtronicNeuro.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 100 participants
- Enrollment target
- 8
- Study locations
Study Summary
The purpose of this study is to characterize the pain coverage capability of the RESTORE spinal cord stimulation (SCS) and assess health outcomes.
Conditions Studied
Interventions
- DEVICE Spinal Cord Stimulation
Study Locations (8)
Texas
- Contact Medtronic for Exact Location - Dallas
- Contact Medtronic for Exact Location - San Antonio
Illinois
- Contact Medtronic for Exact Location - Chicago
Indiana
- Contact Medtronic for Exact Location - Indianapolis
Missouri
- Contact Medtronic for Exact Location - Kansas City
New York
- Contact Medtronic for Exact Location - Syosset
Oregon
- Contact Medtronic for Exact Location - Eugene
West Virginia
- Contact Medtronic for Exact Location - Huntington
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2005-01 |
| Est. Completion | 2007-08 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00200122
The ClinicalTrials.gov registry entry for NCT00200122 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is MedtronicNeuro, which has 51 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Chronic Refractory Pain Associated With Failed Back Surgery Syndrome, Epidural Fibrosis, Peripheral Causalgia, Complex Regional Pain Syndrome appearing as the primary indexed condition, and to 1 intervention - of which Spinal Cord Stimulation is the first listed.
NCT00200122 reports 8 study locations spanning 7 distinct geographic areas - top geographies include Texas, Illinois, Indiana.
Frequently Asked Questions
What is clinical trial NCT00200122 about?
NCT00200122 is a clinical study titled "Restore Claims Characterization Study". The purpose of this study is to characterize the pain coverage capability of the RESTORE spinal cord stimulation (SCS) and assess health outcomes.
What is the current status of trial NCT00200122?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 100 participants. The study started on 2005-01. Estimated completion is 2007-08.
What conditions does trial NCT00200122 study?
This clinical trial studies the following conditions: Chronic Refractory Pain Associated With Failed Back Surgery Syndrome, Epidural Fibrosis, Peripheral Causalgia, Complex Regional Pain Syndrome.
What interventions are being tested in trial NCT00200122?
The interventions under investigation include: Spinal Cord Stimulation (DEVICE).
Who is sponsoring clinical trial NCT00200122?
This trial is sponsored by MedtronicNeuro, which has 51 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00200122 being conducted?
This trial has 8 study locations across Illinois, Indiana, Missouri, New York, Oregon. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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