← Eichor
Study identifier: NCT06142669 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

EVOLUTION® Revision STEMMED CS Post Market Clinical Follow-up Study Protocol

Condition: Joint Diseases  ·  Sponsor: MicroPort Orthopedics Inc.

PhaseN/A
Planned participants45
Who can joinAll sexes, 21 Years to no upper limit
Healthy volunteersNo

About this study

MicroPort (MPO) is conducting this PMCF study to evaluate the safety and effectiveness of its EVOLUTION® Revision Tibial System and EVOLUTION® Revision STEMMED CS Femur with the EVOLUTION® MP CS Tibial Insert. This type of study is required by regulatory authorities for all devices that have been approved in Europe to evaluate the medium and long-term clinical evidence.

This description comes directly from the study's public registry record.

Talk to the study team

JoAnna-Marie N Becker, BS  ·  +1 901 290 5280  ·  joannamarie.becker@ortho.microport.com

Pietro Randelli, Prof  ·  +39-335-5292-622  ·  pietro.randelli@unimi.it

Always discuss trial participation with your own doctor first.

Locations (1)

Gaetano Pini Orthopedic InstituteMilan, Piazza C. Ferrari 1 20122 Milan, ItalyRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06142669