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Clinical Trial Summary

A retrospective post-market data collection study of the following implant devices : - DARCO™ Headed Cannulated Screw - ORTHOLOC™ 3Di Recon-Midfoot/Flatfoot System - ORTHOLOCTM 3Di 2 Foot Reconstruction System: CROSSCHECK™ Module


Clinical Trial Description

A retrospective post-market data collection study designed to collect safety and performance Standard of Care data on patients who have undergone routine lower limb surgery that involved one of the following implant devices as per the indication for use: - DARCO™ Headed Cannulated Screw - ORTHOLOC™ 3Di Recon-Midfoot/Flatfoot System - ORTHOLOCTM 3Di 2 Foot Reconstruction System: CROSSCHECK™ Module ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05234801
Study type Observational
Source Robert Jones and Agnes Hunt Orthopaedic and District NHS Trust
Contact
Status Active, not recruiting
Phase
Start date March 30, 2022
Completion date July 30, 2022

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