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Correction of Hallux Valgus With the Nexis® PECA Bunion Implantable Osteosynthesis Medical Device — PECA  

Hallux Valgus Clinical Trial

Official title:
Correction of Hallux Valgus With the Nexis® PECA Bunion Implantable Osteosynthesis Medical Device : Evaluation of Quality of Life Scores, Angular Correction, Bone Consolidation and Occurrence of Adverse Events

Clinical Trial Summary

The Nexis® screw system is a range of osteosynthesis screws for the foot. Nexis® Bunion Screws are Class IIb implantable medical devices. The primary objective of the study is to confirm the performance and effectiveness of the device under investigation for the correction of hallux valgus with the evaluation functional capacities of the patient's foot. It will be assessed with "general sub-score" of the EFAS questionnaire determined during the postoperative visit at 6 months. The evaluation of quality of life scores, angular correction, bone consolidation and occurrence of adverse events will also be carried out.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05361317
Study type Interventional
Source Novastep
Contact Flora Peyret
Phone +33 (0) 2 99 33 86 50
Email flora.peyret@novastep-ortho.com
Status Recruiting
Phase N/A
Start date June 13, 2022
Completion date August 13, 2025
View Details
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