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Post-Market, Long-Term Follow Up of Mobi-C® Cervical Disc for One and Two Level Treatment of Cervical Disc Disease
NCT03077516 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to evaluate clinical and patient-reported outcomes at 10 years following surgery for a cohort of Mobi-C subjects treated on the IDE/Post Approval studies
Conditions Studied
Interventions
- DEVICE Mobi-C
Study Locations (8)
California
- Orange County Neurosurgical Associates — Laguna Hills
- Desert Orthopedic Center — Rancho Mirage
- UC Davis Spine Center — Sacramento
- The Spine Institute — Santa Monica
Texas
- Texas Back Institute — Plano
- Texas Spine and Joint Hospital — Tyler
Indiana
- Orthopedics Northeast — Fort Wayne
Louisiana
- Spine Institute of Louisiana — Shreveport
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 216 participants |
| Start Date | 2016-11 |
| Est. Completion | 2019-10-31 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03077516
The ClinicalTrials.gov registry entry for NCT03077516 describes a study currently listed as completed. It is categorized as an unspecified phase, 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 216 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is LDR Spine U, 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 2 conditions, with Cervical Disc Disease appearing as the primary indexed condition, and to 1 intervention — of which Mobi-C 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: NCT03077516 reports 8 study locations spanning 4 distinct geographic areas — top geographies include California, Texas, Indiana. 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 NCT03077516 about?
NCT03077516 is a clinical study titled "Post-Market, Long-Term Follow Up of Mobi-C® Cervical Disc for One and Two Level Treatment of Cervical Disc Disease". The purpose of this study is to evaluate clinical and patient-reported outcomes at 10 years following surgery for a cohort of Mobi-C subjects treated on the IDE/Post Approval studies
What is the current status of trial NCT03077516?
This trial is currently completed. The enrollment target is 216 participants. The study started on 2016-11. Estimated completion is 2019-10-31.
What conditions does trial NCT03077516 study?
This clinical trial studies the following conditions: Cervical Disc Disease, Cervical Disc Degeneration. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT03077516?
The interventions under investigation include: Mobi-C (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT03077516?
This trial is sponsored by LDR Spine U, 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 NCT03077516 being conducted?
This trial has 8 study locations across California, Indiana, Louisiana, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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