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RECRUITING
NCT05206981

Device Global Registry for the IlluminOss Bone Stabilization System

Sponsor: IlluminOss Medical, Inc.

View on ClinicalTrials.gov

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

Interventions

DEVICE

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