Patient Specific Talus Spacer Post Approval Study

NCT05364606 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2024-11-07

No results posted yet for this study

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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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05364606 on ClinicalTrials.gov