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RECRUITING NA

Investigation of DEXA-C Anterior Cervical Interbody System

NCT05883436 · View on ClinicalTrials.gov ↗

Study Summary

FDA Cleared interbody product for the cervical spine, designed to match a patients DEXA scan for increase in fusion rate.

Conditions Studied

Interventions

  • DEVICE DEXA-C Cervical Interbody System

Study Locations (4)

California

  • UCI Center for Clinical Research — Orange

Kentucky

  • Orthopaedic Institute of Western KY — Paducah

Louisiana

  • Koga Neurosurgery — Covington

Oklahoma

  • Optima Orthopedics — Oklahoma City

Trial Details

FieldValue
Enrollment Target 80 participants
Start Date 2023-02-22
Est. Completion 2027-02-22
Phase NA

Sponsor

Aurora Spine and Pain

32 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05883436

The ClinicalTrials.gov registry entry for NCT05883436 describes a study currently listed as 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 80 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Aurora Spine and Pain, which has 32 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 1 intervention — of which DEXA-C Cervical Interbody System 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: NCT05883436 reports 4 study locations spanning 4 distinct geographic areas — top geographies include California, Kentucky, Louisiana. 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 NCT05883436 about?

NCT05883436 is a clinical study titled "Investigation of DEXA-C Anterior Cervical Interbody System". FDA Cleared interbody product for the cervical spine, designed to match a patients DEXA scan for increase in fusion rate.

What is the current status of trial NCT05883436?

This trial is currently recruiting. It is a NA study. The enrollment target is 80 participants. The study started on 2023-02-22. Estimated completion is 2027-02-22.

What conditions does trial NCT05883436 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 NCT05883436?

The interventions under investigation include: DEXA-C Cervical Interbody System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05883436?

This trial is sponsored by Aurora Spine and Pain, which has 32 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05883436 being conducted?

This trial has 4 study locations across California, Kentucky, Louisiana, Oklahoma. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial