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NCT01484366 · ClinicalTrials.gov registry record · NA
Forearm Shaft Fractures: Plating of Radius and Ulna Versus Plating of Radius and Nailing of Ulna
A NA study, sponsored by Florida Orthopaedic Institute.
- Terminated
- Registry status
- NA
- Development phase
- 13
- Enrollment target
NCT01484366 is a NA study that was terminated before completion, run by Florida Orthopaedic Institute. The registered enrollment target is 13 participants.
The verdict
NCT01484366, a NA study, was terminated before completion, sponsored by Florida Orthopaedic Institute.
- TERMINATED
- Registry status
- NA
- Development phase
- 13 participants
- Enrollment target
Study Summary
The hypothesis is that intramedullary nailing of the ulna and plating of the radius will result in a superior outcome as evidenced by two primary end points: 1. a lower rate of implant pain 2. a lower re-operation rate to remove painful hardware.
Interventions
- PROCEDURE intramedullary nailing and plating
- PROCEDURE plating
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 13 participants |
| Start Date | 2010-09 |
| Est. Completion | 2013-02 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01484366
The ClinicalTrials.gov registry entry for NCT01484366 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 13 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Florida Orthopaedic Institute, which has 5 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which intramedullary nailing and plating is the first listed.
NCT01484366 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01484366 about?
NCT01484366 is a clinical study titled "Forearm Shaft Fractures: Plating of Radius and Ulna Versus Plating of Radius and Nailing of Ulna". The hypothesis is that intramedullary nailing of the ulna and plating of the radius will result in a superior outcome as evidenced by two primary end points: 1. a lower rate of implant pain 2. a lower re-operation rate to remove painful hardware.
What is the current status of trial NCT01484366?
This trial is currently terminated. It is a NA study. The enrollment target is 13 participants. The study started on 2010-09. Estimated completion is 2013-02.
What interventions are being tested in trial NCT01484366?
The interventions under investigation include: intramedullary nailing and plating (PROCEDURE), plating (PROCEDURE).
Who is sponsoring clinical trial NCT01484366?
This trial is sponsored by Florida Orthopaedic Institute, which has 5 total clinical trials registered on ClinicalTrials.gov.
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