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Clinical Trial Summary

This PMCF study is designed to collect safety and efficacy data on hip hemiarthroplasty surgeries with Corin BiPolar-i shell and the Oceane+ or Meije Duo femoral stem up to 10 years.


Clinical Trial Description

As part of the current clinical remediation work under the new Medical Device Regulation (MDR), limited data have been identified to support the hemiarthroplasty indication for some of Corin femoral stems. Therefore, this PMCF study has been implemented to collect safety and performance data on hip hemiarthroplasty surgeries with Corin BiPolar-i shell and the Oceane+ or Meije Duo femoral stem up to 10 years. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05686278
Study type Observational
Source Corin
Contact Vanessa GRIMAUD
Phone 0667267075
Email vanessa.grimaud@coringroup.com
Status Recruiting
Phase
Start date June 29, 2023
Completion date September 2033

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