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Study identifier: NCT05206981 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Device Global Registry for the IlluminOss Bone Stabilization System

Condition: Traumatic Fracture · Pathological Fracture  ·  Sponsor: IlluminOss Medical, Inc.

PhaseN/A
Planned participants300
Who can joinAll sexes, 50 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Lisa Holt, PhD  ·  401-714-0008  ·  lholt@illuminoss.com

Caitlin Smith, MPH  ·  401-714-0008  ·  csmith@illuminoss.com

Always discuss trial participation with your own doctor first.

Locations (16)

Gulf OrthopedicsMobile, Alabama, United StatesCompleted
Cedars-Sinai Medical CenterLos Angeles, California, United StatesRecruiting
Presbyterian St Luke's Medical CtrDenver, Colorado, United StatesRecruiting
University of Miami HospitalMiami, Florida, United StatesRecruiting
Weston Outpatient Surgical CenterWeston, Florida, United StatesRecruiting
Parkview HealthFort Wayne, Indiana, United StatesWithdrawn
Jacobi Medical CenterThe Bronx, New York, United StatesRecruiting
Mission HospitalAsheville, North Carolina, United StatesWithdrawn
Wake Forest Baptist HealthWinston-Salem, North Carolina, United StatesRecruiting
Temple University HospitalPhiladelphia, Pennsylvania, United StatesRecruiting
University of Pittsburgh Medical CenterPittsburgh, Pennsylvania, United StatesRecruiting
Ortho Rhode IslandWakefield, Rhode Island, United StatesRecruiting

+ 4 more locations — full list on the registry record.

Follow this study

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Source record: clinicaltrials.gov/study/NCT05206981