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NCT00759057 · ClinicalTrials.gov registry record · Phase 3
A Clinical Study of the Dynesys(R) Spinal System
A Phase 3 study, sponsored by Zimmer Biomet.
- Terminated
- Registry status
- Phase 3
- Development phase
- 399
- Enrollment target
NCT00759057 is a Phase 3 study that was terminated before completion, run by Zimmer Biomet. The registered enrollment target is 399 participants.
The verdict
NCT00759057, a Phase 3 study, was terminated before completion, sponsored by Zimmer Biomet.
- TERMINATED
- Registry status
- Phase 3
- Development phase
- 399 participants
- Enrollment target
Study Summary
This non-inferiority study will compare the clinical outcomes of subjects implanted with the Dynesys Spinal System versus the clinical outcomes of subjects implanted with an instrumented posterior lateral spinal fusion.
Interventions
- DEVICE Posterior Pedicle Screw System
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 399 participants |
| Start Date | 2003-03 |
| Est. Completion | 2015-12 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00759057
The ClinicalTrials.gov registry entry for NCT00759057 describes a study currently listed as terminated, categorized as Phase 3. The registered enrollment target is 399 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Zimmer Biomet, which has 115 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Posterior Pedicle Screw System is the first listed.
NCT00759057 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00759057 about?
NCT00759057 is a clinical study titled "A Clinical Study of the Dynesys(R) Spinal System". This non-inferiority study will compare the clinical outcomes of subjects implanted with the Dynesys Spinal System versus the clinical outcomes of subjects implanted with an instrumented posterior lateral spinal fusion.
What is the current status of trial NCT00759057?
This trial is currently terminated. It is a Phase 3 study. The enrollment target is 399 participants. The study started on 2003-03. Estimated completion is 2015-12.
What interventions are being tested in trial NCT00759057?
The interventions under investigation include: Posterior Pedicle Screw System (DEVICE).
Who is sponsoring clinical trial NCT00759057?
This trial is sponsored by Zimmer Biomet, which has 115 total clinical trials registered on ClinicalTrials.gov.
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