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NCT05883436 · ClinicalTrials.gov registry record · NA
Investigation of DEXA-C Anterior Cervical Interbody System
A NA study of Degenerative Disc Disease, sponsored by Aurora Spine and Pain.
- Recruiting
- Registry status
- NA
- Development phase
- 80
- Enrollment target
- 4
- Study locations
NCT05883436 is a NA study of Degenerative Disc Disease that is actively recruiting participants, run by Aurora Spine and Pain. The registered enrollment target is 80 participants, below the 167-participant average among 42 other Degenerative Disc Disease trials with a reported enrollment target (52% lower). The trial reports 4 study locations across 4 states.
The verdict
NCT05883436, a NA study of Degenerative Disc Disease, is actively recruiting participants, sponsored by Aurora Spine and Pain.
- RECRUITING
- Registry status
- NA
- Development phase
- 80 participants
- Enrollment target
- 4
- Study locations
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
| Field | Value |
|---|---|
| Enrollment Target | 80 participants |
| Start Date | 2023-02-22 |
| Est. Completion | 2027-02-22 |
| Phase | NA |
Interested in This Trial?
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, categorized as NA. The registered enrollment target is 80 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 167-participant average among 42 other Degenerative Disc Disease trials with a reported enrollment target (52% lower). The listed sponsor is Aurora Spine and Pain, which has 1 total studies on file at ClinicalTrials.gov.
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.
NCT05883436 reports 4 study locations spanning 4 distinct geographic areas - top geographies include California, Kentucky, Louisiana.
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.
What interventions are being tested in trial NCT05883436?
The interventions under investigation include: DEXA-C Cervical Interbody System (DEVICE).
Who is sponsoring clinical trial NCT05883436?
This trial is sponsored by Aurora Spine and Pain, which has 1 total clinical trials registered on ClinicalTrials.gov.
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.
Learn More About Clinical Trials
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Read our methodology - how this data is sourced, computed, and verified.
Related
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