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NCT04229017 · ClinicalTrials.gov registry record · NA
Study of Posterior Cervical Stabilization System (PCSS) as Part of Circumferential Fusion to Treat Multilevel DDD
A NA study of Degenerative Disc Disease, sponsored by Providence Medical Technology.
- Active
- Registry status
- NA
- Development phase
- 236
- Enrollment target
- 17
- Study locations
NCT04229017: Active NA study of Degenerative Disc Disease, sponsored by Providence Medical Technology.
NCT04229017 is a NA study of Degenerative Disc Disease that is active but no longer recruiting, run by Providence Medical Technology. The registered enrollment target is 236 participants, above the 163-participant average among 42 other Degenerative Disc Disease trials with a reported enrollment target (45% higher). The trial reports 17 study locations across 12 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT04229017, a NA study of Degenerative Disc Disease, is active but no longer recruiting, sponsored by Providence Medical Technology.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 236 participants
- Enrollment target
- 17
- Study locations
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.
Primary Outcome
An individual subject is considered a fusion success if there is evidence of bridging trabecular bone across endplates and \< 2° total angular motion
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 |
What the registry record for NCT04229017 still lists
NCT04229017 is an interventional study that assigns participants to a tested intervention. The registered 236 participants enrollment target is mid-sized for trials with a published cap, above the 163-participant average among 42 other Degenerative Disc Disease trials with a reported enrollment target (45% higher).
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.
NCT04229017 lists 17 locations in 12 states (Louisiana, North Carolina, California).
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.
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).
Who is sponsoring clinical trial NCT04229017?
This trial is sponsored by Providence Medical Technology, which has 2 total clinical trials registered on ClinicalTrials.gov.
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.
Learn More About Clinical Trials
Similar trials for Degenerative Disc Disease
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT04229017's enrollment target sits among peer trials
236 10th of 42 higher than 33 of 42 other Degenerative Disc Disease trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Degenerative Disc Disease trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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Investigation of DEXA-C Anterior Cervical Interbody System
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Evaluation of Safety and Effectiveness of Primary Hybrid Construct of Mobi-C and ACDF in the Treatment of Two-level Symptomatic Degenerative Disc Disease in the Cervical Spine.
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MagnetOs Flex Matrix Compared to Trinity Elite Mixed With Local Autograft in Patients Undergoing up to Four-level Instrumented Posterolateral Fusion
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