A Clinical Study Carried Out in Patients Operated With Calcanail®

Status Completed

Clinical Trial Summary

This study is part of the Post-Market Clinical Follow-up process for the Calcanail medical device; the objective of which is to collect data on the safety and performance of the device after it has been placed on the market. The primary objective of this study is to evaluate the safety of the device. The secondary objectives are to evaluate the clinical performance and safety of the device. This is a research not involving the human person: observational study, retrospective, monocentric, non-comparative and national. 84 patients will be included in the study.

Clinical Trial Description

The CALCANAIL nail is an osteosynthesis nail intended for the repair of articular fractures of the calcaneus, deformities of the hindfoot and arthrosis of the hindfoot. This study aims to answer specific questions about the clinical performance, efficacy or safety of the medical device when used in accordance with its instructions for use. It will also enable us to better detect rare adverse events if necessary, as well as medium-term results. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06234358
Study type	Observational
Source	FH ORTHO
Contact
Status	Completed
Phase
Start date	August 1, 2022
Completion date	February 1, 2023

View Details

See also
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