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Post Market Clinical Follow-up Study Protocol for PROFEMUR® Xm Femoral Stems

Joint Disease Clinical Trial

Official title:
Post Market Clinical Follow-up Study Protocol for PROFEMUR® Xm Femoral Stems

Clinical Trial Summary

MicroPort Orthopedics (MPO) is conducting this post market clinical follow-up (PMCF) study to evaluate the safety and efficacy of its total hip arthroplasty (THA) and resurfacing components marketed in the European Union (EU). These types of studies are required by regulatory authorities for all THA and resurfacing devices that do not have medium to long-term clinical evidence available at the time of gaining approval to market in the EU. This study has been designed in accordance with the medial device directives (MEDDEV) 2.12/2 rev 2.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02309593
Study type Observational
Source MicroPort Orthopedics Inc.
Contact
Status Terminated
Phase
Start date December 2014
Completion date December 21, 2021
View Details
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