Paragon 28
Humanitarian Device Exemption Approved Patient Specific Talus Spacer Post Approval Study.
Avascular Necrosis of the Talus
Patient Specific Talus Spacer
This is a Humanitarian Device Exemption (HDE) approved device called the Patient Specific Talus Spacer. This is a post approval study to determine the safety and probable benefit of the Patient Specific Talus Spacer in commercial use. The Patient Specific Talus Spacer is a solid polished replica of the patient's bone to allow the patient to regain motion and reduce pain.}}
Study Type : | Observational |
Estimated Enrollment : | 50 participants |
Official Title : | Patient Specific Talus Spacer Post Approval Study |
Actual Study Start Date : | July 8, 2022 |
Estimated Primary Completion Date : | August 30, 2029 |
Estimated Study Completion Date : | November 30, 2029 |
Information not available for Arms and Intervention/treatment
Ages Eligible for Study: | 21 Years |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Want to participate in this study, select a site at your convenience, send yourself email to get contact details and prescreening steps.
Recruiting
Redwood Orthopaedics
Santa Rosa, California, United States, 95403
Recruiting
Fort Wayne Orthopedics
Fort Wayne, Indiana, United States, 46804
Recruiting
Mercy Institute for Foot & Ankle Reconstruction
Baltimore, Maryland, United States, 21202
Recruiting
Duke Orthopaedics Arringdon
Morrisville, North Carolina, United States, 27560
Recruiting
Medical University of South Carolina
Charleston, South Carolina, United States, 29425
Recruiting
UT Physicians Orthopedics - Pearland
Pearland, Texas, United States, 77584