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SUCCESS (SelUtion, Safety, effiCaCy, hEalth economicS and promS) PTA Study — SUCCESS PTA  

Peripheral Artery Disease Clinical Trial

Official title:
SUCCESS (SelUtion, Safety, effiCaCy, hEalth economicS and promS) PTA Study

Clinical Trial Summary

Open label, real-world, prospective, multi-center, single arm, post-market surveillance study of the SELUTION SLR™ (Sustained Limus Release) drug eluting balloon (DEB).

Clinical Trial Description

Open label, real-world, prospective, multi-center, single arm, post-market surveillance study of the SELUTION SLR™ (Sustained Limus Release) drug eluting balloon (DEB). This study will capture data from the use of the SELUTION SLR according to its approved labelling. Each indication for use will have a specific data sets in addition to generic data sets that are common across all indications. Patients will be followed for 5 years post-procedure to obtain safety and efficacy data. A health economic analysis will be made comparing data between countries within the study and to published data for existing treatment options. Generic and disease specific Patient Reported Outcome Measures (PROMs) will be used to measure the impact of the intervention on the overall health status of patients. Imaging data collection for patients whose standard of care includes imaging follow-up will be captured and analysed. Data will be collected from any subject who receives a CE marked device for treatment of a peripheral (i.e. non-cardiovascular) vascular lesion. Data analysis will be stratified by lesion location. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04776434
Study type Interventional
Source M.A. Med Alliance S.A.
Contact
Status Active, not recruiting
Phase N/A
Start date February 8, 2021
Completion date December 31, 2028
View Details
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