ProChondrix® CR Articular Cartilage Restoration Evaluation (PACE) Registry

Status Terminated

Clinical Trial Summary

The primary objective of this registry is to obtain long-term outcomes on ProChondrix CR in cartilage repair procedures of the knee, ankle, foot and hip.

Clinical Trial Description

This multi-center, observational registry will be used to evaluate the effectiveness of ProChondrix CR in patients who undergo treatment for an articular cartilage defect in the knee, ankle, foot or hip. This registry will be performed at up to 30 clinical sites across the United States. Patient follow-up will occur following an articular cartilage repair procedure in which the patient receives ProChondrix CR. During this follow-up period, each patient will be evaluated at least four (4) times at: 3, 6, 12 and 24 months after surgical intervention and will continue annually for as long as patients are willing to fill out questionnaires and outcomes assessments up to 10 years post operatively. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04301258
Study type	Observational [Patient Registry]
Source	AlloSource
Contact
Status	Terminated
Phase
Start date	January 6, 2020
Completion date	September 14, 2023

View Details

See also
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