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Evaluation of Standard of Care Practices, Procedural Outcomes and In-hospital Complications of Peripheral Endovascular Procedures — BIO-OSCAR SOC  

Peripheral Arterial Disease Clinical Trial

Official title:
A Prospective, Multicenter, Observational Study Evaluating Standard of Care Practices, Procedural Outcomes, and In-hospital Complications of Endovascular Procedures for Treatment of Atherosclerotic Lesions in the Infrainguinal Arteries

Clinical Trial Summary

Significant advances in dedicated materials and techniques along with increased operator experience led to a significant increment in procedural success rate of peripheral endovascular interventions, exceeding 90% in expert hands with reported low procedural complication rates. However, there are still lack of data on procedural outcomes, in-hospital complications, and resource utilization on treatment of (complex) lesions in the femoral, popliteal and infrapopliteal artery in the real-world condition in Europe.

Clinical Trial Description

The study will enroll consecutive eligible subjects who have peripheral artery disease (PAD) requiring endovascular treatment of de-novo and restenotic atherosclerotic lesions in femoral, popliteal and infrapopliteal arteries. The purpose of this prospective, multicenter, observational European Study is to evaluate the standard of care practices, procedural outcomes, and in-hospital complications of endovascular peripheral interventions for treatment of lesions in the femoral, popliteal and infrapopliteal arteries. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05831319
Study type Observational
Source Biotronik AG
Contact Helene Kuissu, PharmD
Phone +41 79 808 2147
Email adhoc-pvi-clinical-team@mscdigitaloffice.onmicrosoft.com
Status Recruiting
Phase
Start date May 29, 2023
Completion date July 2024
View Details
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