BPK-S Integration (Ceramic) Post Market Clinical Follow-Up

NCT03097471 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 40

Last updated 2017-03-31

No results posted yet for this study

Summary

Post-market prospective clinical study with a medical device. Data from patients that routinely receive a primary BPK-S-integration knee implant made of ceramic will be documented with a follow-up time of 2 years.

Conditions

  • Restoration if Knee Joint Function

Interventions

DEVICE

BPK-S Integration (Ceramic)

primary total knee endoprosthesis

Sponsors & Collaborators

  • Klemens Trieb

    lead OTHER

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-05-31
Primary Completion
2017-10-31
Completion
2018-03-31

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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 NCT03097471 on ClinicalTrials.gov