Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
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 is a clinical trial that was terminated before completion, run by Zimmer Biomet. The registered enrollment target is 8 participants.
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.
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 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01750840
The ClinicalTrials.gov registry entry for NCT01750840 describes a study currently listed as terminated, categorized as an unspecified phase. The registered enrollment target is 8 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 3 interventions - of which Biomet® EBI Bone Healing System is the first listed.
NCT01750840 reports 0 study locations.
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.
Learn More About Clinical Trials
Explore more on PlainTrial
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.