BioPoly® RS Partial Resurfacing Patella Registry Study

NCT02991300 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 12

Last updated 2025-04-16

No results posted yet for this study

Summary

The data registry will increase the knowledge of outcomes for treatment of focal cartilage defects of the patella treated with the BioPoly RS Patella Implant and will allow monitoring of the clinical safety and performance of the device and surgical implantation kit

Conditions

  • Cartilage Disease

Interventions

DEVICE

BioPoly RS Partial Resurfacing Patella Implant

Sponsors & Collaborators

  • BioPoly LLC

    lead INDUSTRY

Principal Investigators

  • Dinesh Nathwani, MD · Charing Cross Hospital

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-09-30
Primary Completion
2024-12-31
Completion
2024-12-31

Countries

  • United Kingdom

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 NCT02991300 on ClinicalTrials.gov