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Device Global Registry for the IlluminOss Bone Stabilization System
Sponsor: IlluminOss Medical, Inc.
Summary
This is a multi-center, observational patient registry. The primary objective of the study is to collect safety and performance data on the IlluminOss Device when used to provide stabilization and alignment for the treatment of traumatic or impending and pathologic fractures.
Official title: IlluminOss Device Global Registry - A Prospective, Post-Market, Multi-Center Evaluation of the Clinical Outcomes of the IlluminOss Device
Key Details
Gender
All
Age Range
50 Years - Any
Study Type
OBSERVATIONAL
Enrollment
300
Start Date
2021-06-11
Completion Date
2026-12
Last Updated
2025-04-30
Healthy Volunteers
No
Conditions
Interventions
IlluminOss Device
Patients may enroll in the registry if they have been implanted (retrospective) or will be implanted (prospective) with the IlluminOss device.
Locations (16)
Gulf Orthopedics
Mobile, Alabama, United States
Cedars-Sinai Medical Center
Los Angeles, California, United States
Presbyterian St Luke's Medical Ctr
Denver, Colorado, United States
University of Miami Hospital
Miami, Florida, United States
Weston Outpatient Surgical Center
Weston, Florida, United States
Parkview Health
Fort Wayne, Indiana, United States
Jacobi Medical Center
The Bronx, New York, United States
Mission Hospital
Asheville, North Carolina, United States
Wake Forest Baptist Health
Winston-Salem, North Carolina, United States
Temple University Hospital
Philadelphia, Pennsylvania, United States
University of Pittsburgh Medical Center
Pittsburgh, Pennsylvania, United States
Ortho Rhode Island
Wakefield, Rhode Island, United States
Memorial Hermann Hospital
Katy, Texas, United States
St Vinzenz Hospital
Cologne, Germany
Johannes Wesling Hospital Minden
Minden, Germany
Petrus Hospital
Wuppertal, Germany