Device Global Registry for the IlluminOss Bone Stabilization System
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age50+
SponsorIlluminOss Medical, Inc.
About this trial
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.
Eligibility criteria
Qualifiers
Patient has been deemed a candidate for the IlluminOss device
Patient is male or non-pregnant female
Patient is willing and able to comply with the postoperative scheduled clinical and radiographic evaluations
Patient is willing and able to give informed consent if required
Disqualifiers
an active or incompletely treated infection that could involve the site where the device will be implanted;
are allergic to any of the implant materials or to dental glue;
have an intramedullary canal measuring smaller than the diameter of the delivery sheath provided at the site of the fracture;
distant foci of infections which may spread to the implant site, have open fractures with severe contamination;
Trial design
Treatments tested in this trial
- IlluminOss Device
Treatment groups
No treatment groups listed
Sponsors and collaborators
Source ClinicalTrials.gov