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Clinical Trial Summary

Sponsor is conducting this post market clinical study to evaluate the safety and effectiveness of its PROFEMUR® Preserve Classic Femoral Stem. This type of study is required by regulatory authorities for all devices that have been approved in Europe (EU) to evaluate the medium and long-term clinical evidence. This study has been designed in accordance with MEDDEV2.12/2 (European Medical Device Vigilance System) rev2 and ISO (International Organization of Standardization) 14155:2011 guidelines.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04147559
Study type Observational
Source MicroPort Orthopedics Inc.
Contact
Status Enrolling by invitation
Phase
Start date October 21, 2020
Completion date November 1, 2033

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