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Clinical Trial Summary

The rationale of this study is to confirm and support the clinical safety and performance of any of these products in a real-world population of 209 patients who underwent an endovascular intervention within standard-of-care of the iliacofemoral artery and renal artery, using at least one of the investigational products from iVascular.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05902923
Study type Observational
Source iVascular S.L.U.
Contact Mieke Ramsdonck
Phone +32 479 64 37 60
Email mieke.ramsdonck@fcre.eu
Status Recruiting
Phase
Start date August 1, 2023
Completion date August 2027

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