RecruitingNCT05364606

Patient Specific Talus Spacer Post Approval Study


Sponsor

Paragon 28

Enrollment

50 participants

Start Date

Jul 8, 2022

Study Type

OBSERVATIONAL

Conditions

Summary

Humanitarian Device Exemption Approved Patient Specific Talus Spacer Post Approval Study.


Eligibility

Min Age: 21 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a medical device called Patient Specific Talus Spacer for people with avascular necrosis of the talus. The study is currently recruiting participants at 6 locations. People eligible for this study include aged 21 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICEPatient Specific Talus Spacer

Patient Specific Talus Spacer is a solid polished replica of the patient's bone.


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

View Full Details on ClinicalTrials.gov

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NCT05364606


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