RecruitingNCT05364606
Patient Specific Talus Spacer Post Approval Study
Studying Avascular necrosis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Paragon 28
- Intervention
- Patient Specific Talus Spacer(device)
- Enrollment
- 50 enrolled
- Eligibility
- 21 years · All sexes
- Timeline
- 2022 – 2029
Study locations (6)
- Redwood Orthopaedics, Santa Rosa, California, United States
- Fort Wayne Orthopedics, Fort Wayne, Indiana, United States
- Mercy Institute for Foot & Ankle Reconstruction, Baltimore, Maryland, United States
- Duke Orthopeadics Arringdon, Morrisville, North Carolina, United States
- Medical University of South Carolina, Charleston, South Carolina, United States
- UT Physicians Orthopedics - Pearland, Pearland, Texas, United States
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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