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Study of Posterior Cervical Stabilization System (PCSS) as Part of Circumferential Fusion to Treat Multilevel DDD
NCT04229017 · View on ClinicalTrials.gov ↗
Study Summary
This study will evaluate the safety and effectiveness of a device called "Posterior Cervical Stabilization System or PCSS" when used along with posterior cervical fusion (PCF) in combination with anterior cervical discectomy and fusion (ACDF) in the treatment of multi-level cervical degenerative disease.
Conditions Studied
Interventions
- PROCEDURE Anterior Cervical Discectomy and Fusion
- DEVICE Posterior Cervical Stabilization System (PCSS)
Study Locations (17)
Louisiana
- Bone and Joint Clinic of Baton Rouge — Baton Rouge
- LSU Health — New Orleans
- Spine Institute of Louisiana — Shreveport
North Carolina
- The University of North Carolina at Chapel Hill — Chapel Hill
- Pinehurst Surgical Clinic — Pinehurst
- Atlantic Neurosurgical & Spine Specialists — Wilmington
California
- Scripps — Encinitas
- OrthoNorCal — Los Gatos
Arizona
- Barrow Neurological Institute — Phoenix
Colorado
- Spine Colorado — Durango
Illinois
- Rush University Medical Center — Chicago
Kentucky
- The Orthopaedic Institute — Paducah
Maryland
- LifeBridge Health - Sinai Hospital of Baltimore — Baltimore
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 236 participants |
| Start Date | 2020-03-18 |
| Est. Completion | 2025-12 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04229017
The ClinicalTrials.gov registry entry for NCT04229017 describes a study currently listed as active not recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 236 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Providence Medical Technology, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Degenerative Disc Disease appearing as the primary indexed condition, and to 2 interventions — of which Anterior Cervical Discectomy and Fusion is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT04229017 reports 17 study locations spanning 12 distinct geographic areas — top geographies include Louisiana, North Carolina, California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT04229017 about?
NCT04229017 is a clinical study titled "Study of Posterior Cervical Stabilization System (PCSS) as Part of Circumferential Fusion to Treat Multilevel DDD". This study will evaluate the safety and effectiveness of a device called "Posterior Cervical Stabilization System or PCSS" when used along with posterior cervical fusion (PCF) in combination with anterior cervical discectomy and fusion (ACDF) in the treatment of multi-level cervical degenerative dis...
What is the current status of trial NCT04229017?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 236 participants. The study started on 2020-03-18. Estimated completion is 2025-12.
What conditions does trial NCT04229017 study?
This clinical trial studies the following conditions: Degenerative Disc Disease. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT04229017?
The interventions under investigation include: Anterior Cervical Discectomy and Fusion (PROCEDURE), Posterior Cervical Stabilization System (PCSS) (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04229017?
This trial is sponsored by Providence Medical Technology, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT04229017 being conducted?
This trial has 17 study locations across Arizona, California, Colorado, Illinois, Kentucky. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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