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Device Global Registry for the IlluminOss Bone Stabilization System

StatusRecruiting
PhaseNot specified
Started
View on ClinicalTrials.gov ↗

Record History

  1. Site details revised at 3 of 16 sitesv12
  2. Primary and study completion dates: Dec 2024 to Dec 2026
    • Site details revised at 6 of 16 sites
    v11
  3. Study sites: 15 to 16v10
  4. Study sites: 13 to 15v9
  5. Site details revised at 1 of 13 sitesv8
Show 6 earlier versionsHide 6 earlier versions
  1. Study sites: 11 to 13v7
  2. Study sites: 10 to 11v6
  3. Study sites: 9 to 10v5
  4. Study sites: 8 to 9v4
  5. Study sites: 4 to 8v3
  6. Study sites: 1 to 4v2
  1. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT05206981
Lead Sponsor IlluminOss Medical, Inc.
Conditions
(from sponsor)		 Traumatic Fracture, Pathological Fracture
Related terms Fractures, Spontaneous
Enrollment 300 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov