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Artoss Prospective Spine Registry Outcomes
NCT04439032 · View on ClinicalTrials.gov ↗
Study Summary
This prospective registry was designed as an observational study to ascertain how commercially available NanoBone Bone Graft is being used by surgeons performing spinal fusion as well as determining relevant patient outcomes.
Conditions Studied
Interventions
- OTHER NanoBone Bone Graft Substitute
Study Locations (6)
Arizona
- OrthoArizona — Chandler
- Sonoran Spine — Tempe
California
- SENTA Clinic — San Diego
Connecticut
- Hartford Health Care — Hartford
Maryland
- OrthoBethesda — Bethesda
Mississippi
- Sam Shamsnia MD Neurosurgery — Biloxi
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 330 participants |
| Start Date | 2020-08-03 |
| Est. Completion | 2025-06-30 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04439032
The ClinicalTrials.gov registry entry for NCT04439032 describes a study currently listed as active not 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 330 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Artoss, which has 3 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 Spinal Fusion appearing as the primary indexed condition, and to 1 intervention — of which NanoBone Bone Graft Substitute 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: NCT04439032 reports 6 study locations spanning 5 distinct geographic areas — top geographies include Arizona, California, Connecticut. 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 NCT04439032 about?
NCT04439032 is a clinical study titled "Artoss Prospective Spine Registry Outcomes". This prospective registry was designed as an observational study to ascertain how commercially available NanoBone Bone Graft is being used by surgeons performing spinal fusion as well as determining relevant patient outcomes.
What is the current status of trial NCT04439032?
This trial is currently active not recruiting. The enrollment target is 330 participants. The study started on 2020-08-03. Estimated completion is 2025-06-30.
What conditions does trial NCT04439032 study?
This clinical trial studies the following conditions: Spinal 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 NCT04439032?
The interventions under investigation include: NanoBone Bone Graft Substitute (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04439032?
This trial is sponsored by Artoss, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT04439032 being conducted?
This trial has 6 study locations across Arizona, California, Connecticut, Maryland, Mississippi. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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