Serranator® Alto Post Market Clinical Follow Up (PMCF) Study

Status Withdrawn

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

Clinical Trial Details

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Status	Withdrawn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

View Details

See also
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