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NCT00443547 · ClinicalTrials.gov registry record
Outcome Study of Patients Treated With Translational Cervical Plate Used to Treat Degenerative Disc Disease
A clinical trial, sponsored by Synthes USA HQ.
- Completed
- Registry status
- 231
- Enrollment target
NCT00443547: Completed study, sponsored by Synthes USA HQ.
NCT00443547 is a clinical trial that has completed, run by Synthes USA HQ. The registered enrollment target is 231 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00443547 has completed, sponsored by Synthes USA HQ.
- COMPLETED
- Registry status
- 231 participants
- Enrollment target
Study Summary
The purpose of this study is to measure the benefits of anterior (from the front) cervical (neck) surgery for degenerative disc disease. The research part of this study is the answering of questionnaires by the patient concerning their quality of life, prior to, and after surgery.
Primary Outcome
Percentage of subjects who were successfully fused per an independent radiographic assessment at all index levels
Interventions
- DEVICE Vectra-T
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 231 participants |
| Start Date | 2006-03-01 |
| Est. Completion | 2011-04-01 |
What the finished NCT00443547 record still lists
NCT00443547 is an observational study that tracks outcomes without assigning an intervention. The registered 231 participants enrollment target is mid-sized for trials with a published cap.
The record links to 0 conditions, and to 1 intervention - of which Vectra-T is the first listed.
NCT00443547 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00443547 about?
NCT00443547 is a clinical study titled "Outcome Study of Patients Treated With Translational Cervical Plate Used to Treat Degenerative Disc Disease". The purpose of this study is to measure the benefits of anterior (from the front) cervical (neck) surgery for degenerative disc disease. The research part of this study is the answering of questionnaires by the patient concerning their quality of life, prior to, and after surgery.
What is the current status of trial NCT00443547?
This trial is currently completed. The enrollment target is 231 participants. The study started on 2006-03-01. Estimated completion is 2011-04-01.
What interventions are being tested in trial NCT00443547?
The interventions under investigation include: Vectra-T (DEVICE).
Who is sponsoring clinical trial NCT00443547?
This trial is sponsored by Synthes USA HQ, which has 7 total clinical trials registered on ClinicalTrials.gov.
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