Patient Specific Talus Spacer Post Approval Study
NCT05364606 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 50
Last updated 2024-11-07
Summary
Humanitarian Device Exemption Approved Patient Specific Talus Spacer Post Approval Study.
Conditions
- Avascular Necrosis of the Talus
Interventions
- DEVICE
-
Patient Specific Talus Spacer
Patient Specific Talus Spacer is a solid polished replica of the patient's bone.
Sponsors & Collaborators
-
Paragon 28
lead INDUSTRY
Eligibility
- Min Age
- 21 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-07-08
- Primary Completion
- 2029-08-30
- Completion
- 2029-11-30
- FDA Device
- Yes
Countries
- United States
Study Locations
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