NCT00823251

IlluminOss Hand Fracture International Clinical Feasibility Study

IlluminOss Medical- Photodynamic Bone Stabilization System- International Study

• Status: Completed
• Phase: Phase 1
• Study type: Interventional
• Enrollment: 4 (actual)
• Sponsor: IlluminOss Medical, Inc. · Industry
• Sex: All
• Age: 18 Years – 80 Years
• Healthy volunteers: Not accepted

Summary

The purpose of this study is to assess the initial safety and technical feasibility of the IlluminOss System in the treatment of fractures of bones in the hand.

Conditions

• Orthopedic Fractures

Interventions

Type	Name	Description
DEVICE	IlluminOss device	The IlluminOss™ Bone Stabilization System is designed to deliver the device to the fracture site via the medullary canal of the bone using percutaneous techniques. Once the device is in place and has spanned the fracture site, the device is expanded and hardened to reduce and stabilize the fracture, to aid in the support and healing of the bone fracture by primary callous formation and remodeling.

Timeline

• Start date: 2008-12-01
• Primary completion: 2009-10-01
• Completion: 2013-02-01
• First posted: 2009-01-15
• Last updated: 2017-06-07

Locations

1 site across 1 country: Chile