MIMICS-3D-USA Registry Study

Status Active, not recruiting

Clinical Trial Summary

The MIMICS-3D-USA Study is a prospective, multicentre, observational study (non-investigational) of the BioMimics 3D Vascular Stent System that evaluates evaluate safety, effectiveness and device performance within a real-world clinical population of patients undergoing femoropopliteal intervention for the treatment of peripheral artery disease.

Clinical Trial Description

The MIMICS-3D-USA Study is designed to enable the collection, analysis, reporting and presentation of data from use of the BioMimics 3D Vascular Stent System purchased by the hospital / institution or office interventional suite and used in accordance with the IFU associated with the product's FDA approval. The intent of this post-market observational study is to increase the understanding of the performance of the BioMimics 3D Vascular Stent System in a larger population of patients representative of a real-world situation within US hospitals, institutions and office-based interventional suites or labs. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04640597
Study type	Observational [Patient Registry]
Source	Veryan Medical Ltd.
Contact
Status	Active, not recruiting
Phase
Start date	December 18, 2020
Completion date	September 4, 2025

View Details

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