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NCT01750840 · ClinicalTrials.gov registry record
A Clinical Registry to Collect Patient Outcome Date for the BIOMET® Stimulator Systems
A clinical trial, sponsored by Zimmer Biomet.
- Terminated
- Registry status
- 8
- Enrollment target
NCT01750840: Clinical Trial study, sponsored by Zimmer Biomet.
NCT01750840 is a clinical trial that was terminated before completion, run by Zimmer Biomet. The registered enrollment target is 8 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01750840 was terminated before completion, sponsored by Zimmer Biomet.
- TERMINATED
- Registry status
- 8 participants
- Enrollment target
Study Summary
The purpose of this clinical registry is to capture data on an ongoing basis from a population of patients who will use Biomet's BHS, OrthoPak and SpinalPak devices.
Primary Outcome
Bone healing was assessed on x-rays and/or CT scan.
Interventions
- DEVICE Biomet® EBI Bone Healing System
- DEVICE Biomet Orthopak® Non-Invasive Bone Growth Stimulator System
- DEVICE Biomet SpinalPak® Non-Invasive Spine Fusion Stimulator
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 8 participants |
| Start Date | 2012-10 |
| Est. Completion | 2013-10 |
Why NCT01750840 stopped before completion
NCT01750840 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 8 participants, a relatively small participant target.
The record links to 0 conditions, and to 3 interventions - of which Biomet® EBI Bone Healing System is the first listed.
NCT01750840 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01750840 about?
NCT01750840 is a clinical study titled "A Clinical Registry to Collect Patient Outcome Date for the BIOMET® Stimulator Systems". The purpose of this clinical registry is to capture data on an ongoing basis from a population of patients who will use Biomet's BHS, OrthoPak and SpinalPak devices.
What is the current status of trial NCT01750840?
This trial is currently terminated. The enrollment target is 8 participants. The study started on 2012-10. Estimated completion is 2013-10.
What interventions are being tested in trial NCT01750840?
The interventions under investigation include: Biomet® EBI Bone Healing System (DEVICE), Biomet Orthopak® Non-Invasive Bone Growth Stimulator System (DEVICE), Biomet SpinalPak® Non-Invasive Spine Fusion Stimulator (DEVICE).
Who is sponsoring clinical trial NCT01750840?
This trial is sponsored by Zimmer Biomet, which has 115 total clinical trials registered on ClinicalTrials.gov.
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