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NCT00637312 · ClinicalTrials.gov registry record · NA
Advent™ Cervical Disc Versus ACDF for Treatment of One Level Degenerative Disc Disease (IDE Study)
A NA study, sponsored by Orthofix.
- Terminated
- Registry status
- NA
- Development phase
- 108
- Enrollment target
NCT00637312 is a NA study that was terminated before completion, run by Orthofix. The registered enrollment target is 108 participants.
The verdict
NCT00637312, a NA study, was terminated before completion, sponsored by Orthofix.
- TERMINATED
- Registry status
- NA
- Development phase
- 108 participants
- Enrollment target
Study Summary
The purpose of this study is to establish the safety and effectiveness of the Advent™ Cervical Disc compared to Anterior Cervical Discectomy and Fusion (ACDF) in treating degenerative disc disease at a single-level in the cervical spine (from C3 to C7) following cervical discectomy in skeletally mature patients (at least 18 years of age).
Interventions
- DEVICE Cervical Artificial Disc (Advent™ Cervical Disc)
- DEVICE Hallmark™ Anterior Cervical Plate System
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 108 participants |
| Start Date | 2008-03 |
| Est. Completion | 2013-02 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00637312
The ClinicalTrials.gov registry entry for NCT00637312 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 108 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Orthofix, which has 14 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Cervical Artificial Disc (Advent™ Cervical Disc) is the first listed.
NCT00637312 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00637312 about?
NCT00637312 is a clinical study titled "Advent™ Cervical Disc Versus ACDF for Treatment of One Level Degenerative Disc Disease (IDE Study)". The purpose of this study is to establish the safety and effectiveness of the Advent™ Cervical Disc compared to Anterior Cervical Discectomy and Fusion (ACDF) in treating degenerative disc disease at a single-level in the cervical spine (from C3 to C7) following cervical discectomy in skeletally mat...
What is the current status of trial NCT00637312?
This trial is currently terminated. It is a NA study. The enrollment target is 108 participants. The study started on 2008-03. Estimated completion is 2013-02.
What interventions are being tested in trial NCT00637312?
The interventions under investigation include: Cervical Artificial Disc (Advent™ Cervical Disc) (DEVICE), Hallmark™ Anterior Cervical Plate System (DEVICE).
Who is sponsoring clinical trial NCT00637312?
This trial is sponsored by Orthofix, which has 14 total clinical trials registered on ClinicalTrials.gov.
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