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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: Clinical Trial Phase 3 study, sponsored by Zimmer Biomet.
NCT00759057 is a Phase 3 study that was terminated before completion, run by Zimmer Biomet. The registered enrollment target is 399 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (48% lower). According to ClinicalTrials.gov, the official US trial registry.
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 |
Why NCT00759057 stopped before completion
NCT00759057 is an interventional study that assigns participants to a tested intervention. The registered 399 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (48% lower).
The record links to 0 conditions, and to 1 intervention - of which Posterior Pedicle Screw System is the first listed.
NCT00759057 does not publish any study locations in the registry export this page uses.
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.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00759057's enrollment target sits among peer trials
399 962nd of 2000 higher than 1,038 of 2,000 other Phase 3 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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