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NUsurface Implant Registry

TerminatedN/A

Sponsor: Phoenix Kinetics

Conditions: Meniscus; Degeneration, Knee Osteoarthritis, Knee Pain Chronic

Countries: Belgium, Germany, Israel, Netherlands

The purpose of this active post-market surveillance clinical registry study is to further characterize the therapeutic effect, the long-term safety and effectiveness of the NUsurface® meniscus implant in the real-world post-marketing setting

Eligibility overview

Sex: ALL

Age: 18 Years to 70 Years

Healthy volunteers: No

Study type: OBSERVATIONAL

Eligibility criteria

Inclusion Criteria:

* New or current treatment with the NUsurface® meniscus implant
* Evidence of a personally signed and dated informed consent document indicating that the subject (or a legally acceptable representative) has been informed of all pertinent aspects of the Registry.

Exclusion Criteria:

* There are no protocol exclusion criteria; all subjects who meet the inclusion criteria are eligible for enrollment.

Locations (6)

Deurne, Belgium
Berlin, Germany
Brandenburg an der Havel, Germany
München, Germany
Ẕerifin, Israel
Maastricht, Netherlands