Status: Recruiting
Device Global Registry for the IlluminOss Bone Stabilization System
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.
Participants needed: 300
Trial details
Age: 50+Biological sex: AllType: ObservationalSponsor: IlluminOss Medical, Inc.Updated: Apr 17, 2026Locations: 16Duration: 1 Year
Eligibility criteria
Patient has been deemed a candidate for the IlluminOss device [+5]
an active or incompletely treated infection that could involve the site where th... [+18]