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Clinical Trial Summary

This is a prospective multicenter study. Subjects will be implanted with a Conformis Hip System. If the surgeon intraoperatively decides to use the Cordera femoral stem, these patients will also be enrolled in the study and tracked as a subset of the Conformis Hip System patient population.The study sites will be located in the United States. The study subjects will be followed for 10 years post implantation.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Clinical Condition Included in the Approved Indications For Use for the Conformis Hip System

NCT number NCT03738462
Study type Observational
Source Restor3D
Contact
Status Terminated
Phase
Start date November 26, 2018
Completion date June 6, 2022