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

TerminatedOBSERVATIONAL
Enrollment

8

Participants

Timeline

Start Date

October 31, 2012

Primary Completion Date

October 31, 2013

Study Completion Date

October 31, 2013

Conditions
Fusion of Spine (Disease)Fractures, Ununited
Interventions
DEVICE

Biomet® EBI Bone Healing System

A pulsed electromagnetic fields electrical stimulation device used for the treatment of fracture nonunions. Designed to be used for 3-10 hours per day with a recommended use of 10 hours per day.

DEVICE

Biomet Orthopak® Non-Invasive Bone Growth Stimulator System

A capacitive coupling electrical stimulation device used for the treatment of fracture nonunions. Designed to be used for 24 hours per day.

DEVICE

Biomet SpinalPak® Non-Invasive Spine Fusion Stimulator

A capacitive coupling electrical stimulation device used as an adjunctive treatment to lumbar spinal fusion. Designed to be used for 24 hours per day.

Trial Locations (1)

08360

Cumberland Orthopedics, Vineland

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Zimmer Biomet

INDUSTRY

NCT01750840 - A Clinical Registry to Collect Patient Outcome Date for the BIOMET® Stimulator Systems | Biotech Hunter | Biotech Hunter