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Clinical Trial Summary

The rationale of this study is to confirm and support the clinical safety and performance of the Oceanus 14pro, Oceanus 18 and Oceanus 35 Balloon Catheters, the Luminor 14m and Luminor 18 Drug Coated Balloons, the Angiolite BTK Sirolimus Eluting Peripheral Stent System and the Sergeant Peripheral Support Catheter in a real-word population of 143 patients who underwent an endovascular intervention the popliteal and/or infrapopliteal arteries within standard-of-care (SOC) where at least 1 of the investigational products from iVascular were used.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05267548
Study type Observational [Patient Registry]
Source iVascular S.L.U.
Contact Mieke Ramsdonck
Email mieke.ramsdonck@FCRE.eu
Status Recruiting
Phase
Start date May 30, 2022
Completion date May 2025