ProChondrix® CR Articular Cartilage Restoration Evaluation (PACE) Registry

Terminated

• Conditions: Cartilage Injury; Cartilage Damage

• Registration Number: NCT04301258
• Lead Sponsor: AlloSource

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2020-3-6
• Last Update Posted: 2 September 2024

Recruitment & Eligibility

• Status: Terminated
• Sex: All
• Target Recruitment: 48

Inclusion Criteria

Inclusion Criteria:<br><br> - Diagnosed by physician to have a cartilage defect in the knee, ankle, foot or hip<br> that requires surgical intervention;<br><br> - Will be having, or has had, a cartilage repair procedure using ProChondrix CR;<br><br> - Has the ability to understand the requirements of the registry, to provide written<br> informed consent and to comply with the registry protocol;<br><br>Exclusion Criteria:<br><br>• Is a ward of the state, prisoner, or transient.

Exclusion Criteria

Not provided

Study & Design

• Study Type: Observational [Patient Registry]
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Long-Term Outcomes of ProChondrix CR