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Prospective SPINE Registry
NCT04176562 · View on ClinicalTrials.gov ↗
Study Summary
This study is a prospective, multi-center, open label registry designed to collect real-world data on performance and safety data on RTI's spine products.
Conditions Studied
Interventions
- DEVICE RTI Spine products
Study Locations (12)
Other
- STENUM Ortho Fachklinik — Ganderkesee
- Wirbelsäulenzentrum Fulda | Main | Kinzig — Gelnhausen
- Katholisches Klinikum Koblenz - Montabaur — Koblenz
- St. Christopherus Krankenhaus - Katholisches Klinikum — Werne
- Hospital Nacional de Parapléjicos — Toledo
Florida
- Florida Back Institute — Boca Raton
- Spine Institute of South Florida — Delray Beach
Indiana
- Indiana Spine Group — Carmel
- DK Orthopedics — Crown Point
Connecticut
- Hartford Hospital — Hartford
Illinois
- Suburban Orthopaedics — Bartlett
Ohio
- Lindner Center for Research & Education at The Christ Hospit — Cincinnati
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 5,000 participants |
| Start Date | 2020-01-28 |
| Est. Completion | 2025-06 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04176562
The ClinicalTrials.gov registry entry for NCT04176562 describes a study currently listed as recruiting. 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 5,000 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Xtant Medical, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 10 conditions, with Spinal Fusion appearing as the primary indexed condition, and to 1 intervention — of which RTI Spine products 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: NCT04176562 reports 12 study locations spanning 6 distinct geographic areas — top geographies include Other, Florida, 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 NCT04176562 about?
NCT04176562 is a clinical study titled "Prospective SPINE Registry". This study is a prospective, multi-center, open label registry designed to collect real-world data on performance and safety data on RTI's spine products.
What is the current status of trial NCT04176562?
This trial is currently recruiting. The enrollment target is 5,000 participants. The study started on 2020-01-28. Estimated completion is 2025-06.
What conditions does trial NCT04176562 study?
This clinical trial studies the following conditions: Spinal Fusion, Spinal Stenosis, Musculoskeletal Diseases, Joint Diseases, Sacroiliac; Fusion. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT04176562?
The interventions under investigation include: RTI Spine products (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04176562?
This trial is sponsored by Xtant Medical, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT04176562 being conducted?
This trial has 12 study locations across Connecticut, Florida, Illinois, Indiana, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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