Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT00586170 · ClinicalTrials.gov registry record · NA
A Double-Blind Study on Adjunctive Use of PEMF in the Treatment of 5th Metatarsal Non-Union Fractures
A NA study, sponsored by Zimmer Biomet.
- Terminated
- Registry status
- NA
- Development phase
- 8
- Enrollment target
NCT00586170 is a NA study that was terminated before completion, run by Zimmer Biomet. The registered enrollment target is 8 participants.
The verdict
NCT00586170, a NA study, was terminated before completion, sponsored by Zimmer Biomet.
- TERMINATED
- Registry status
- NA
- Development phase
- 8 participants
- Enrollment target
Study Summary
The purpose of this study is to analyze the effect of PEMF in surgical reconstruction of 5th metatarsal non-union fractures.
Interventions
- PROCEDURE Surgery
- DEVICE Placebo Device
- DEVICE EBI Bone Healing System
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 8 participants |
| Start Date | 2007-11 |
| Est. Completion | 2012-08 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00586170
The ClinicalTrials.gov registry entry for NCT00586170 describes a study currently listed as terminated, categorized as NA. 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 Surgery is the first listed.
NCT00586170 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00586170 about?
NCT00586170 is a clinical study titled "A Double-Blind Study on Adjunctive Use of PEMF in the Treatment of 5th Metatarsal Non-Union Fractures". The purpose of this study is to analyze the effect of PEMF in surgical reconstruction of 5th metatarsal non-union fractures.
What is the current status of trial NCT00586170?
This trial is currently terminated. It is a NA study. The enrollment target is 8 participants. The study started on 2007-11. Estimated completion is 2012-08.
What interventions are being tested in trial NCT00586170?
The interventions under investigation include: Surgery (PROCEDURE), Placebo Device (DEVICE), EBI Bone Healing System (DEVICE).
Who is sponsoring clinical trial NCT00586170?
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.