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Clinical Trial Summary

The objective of this registry is to collect observational data under local standard of care and evaluate safety and performance of the Serranator® Alto in treatment of peripheral artery disease (PAD), or dysfunctional native or synthetic arteriovenous dialysis fistulae in a real-world scenario.


Clinical Trial Description

Single Arm, multi-center, device registry study capturing de-identified data on a minimum of 100 subjects with peripheral artery disease (PAD) and/or dysfunctional native or synthetic arteriovenous dialysis fistulae. The study will capture acute angiographic data. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03538392
Study type Observational [Patient Registry]
Source Cagent Vascular LLC
Contact
Status Withdrawn
Phase
Start date September 2019
Completion date December 2019

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