A Clinical Registry to Collect Patient Outcome Date for the BIOMET® Stimulator Systems

Fusion of Spine (Disease) Clinical Trial

Official title: A Clinical Registry to Collect Patient Outcome Data for the BIOMET® EBI Bone Healing System, BIOMET® OrthoPak® Non-invasive Bone Growth Stimulator System, and the BIOMET® SpinalPak® Non-Invasive Spine Fusion Stimulator System

Status Terminated

Clinical Trial 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.

Clinical Trial Description

The purpose of this clinical registry is to capture current, real-world, bone specific healing data from the medical records of patients being treated with a Biomet® EBI Bone Healing System (BHS), the Biomet® OrthoPak® Non-Invasive Bone Growth Stimulator System, or the Biomet® SpinalPak® Non-Invasive Spine Fusion Stimulator System. This study will provide current data on the effectiveness of these electrical stimulation devices. ;

Related Conditions & MeSH terms

• Fractures, Ununited
• Fusion of Spine (Disease)

• NCT number: NCT01750840
• Study type: Observational [Patient Registry]
• Source: Zimmer Biomet
• Status: Terminated
• Phase: N/A
• Start date: October 2012
• Completion date: October 2013