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ProChondrix® CR Articular Cartilage Restoration Evaluation (PACE) Registry

NCT04301258 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 48

Last updated 2025-11-21

No results posted yet for this study

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.

Conditions

  • Cartilage Injury
  • Cartilage Damage

Interventions

OTHER

Articular cartilage repair

Patient reported outcomes will be collected on patients who have had a cartilage repair procedure using ProChondrix CR in the knee, hip, foot or ankle.

Sponsors & Collaborators

  • AlloSource

    lead INDUSTRY

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-01-06
Primary Completion
2023-09-14
Completion
2023-09-14

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 NCT04301258 on ClinicalTrials.gov