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SIROOP Registry - A Prospective Registry Study to Evaluate the Outcomes of Coronary Artery Disease Patients Treated With SIROlimus Or Paclitaxel Eluting Balloon Catheters — SIROOP  

Coronary Artery Disease Clinical Trial

Official title:
SIROOP Registry - A Prospective Registry Study to Evaluate the Outcomes of Coronary Artery Disease Patients Treated With SIROlimus Or Paclitaxel Eluting Balloon Catheters

Clinical Trial Summary

The purpose of the SIROOP Registry is to retrospectively and prospectively collect baseline, clinical and procedural characteristics of patients who have undergone PCI and are treated with either currently available sirolimus or paclitaxel coated DCBs (see Table 1), irrespective of clinical presentation as well as to prospectively collect data about their clinical outcomes. Outcomes will be compared in different clinical subgroups. The impact of current DCBs in different clinical settings and coronary artery lesions on cardiovascular outcomes will be assessed.

Clinical Trial Description

Objectives in detail: - To evaluate procedural success, efficacy, performance and clinical outcomes among various patient cohorts, who undergo PCI using currently available DCBs: 1. Periprocedural outcomes/complications, which will be analyzed, include: final result (e.g. residual stenosis, TIMI flow), dissections, perforations, prevalence of thrombus (assessed by angiography and intravascular imaging) 2. Short and long-term clinical outcomes of interest comprise among others: new MI, unstable angina (UA), target lesion failure, target vessel revascularization, target lesion failure/ revascularization, repeat hospitalization, new/worsening heart failure, cardiogenic shock, stroke, bleedings, cardiovascular death and all-cause death. - To describe procedural and clinical performance of various DCB, either alone or in combination with other stent and coronary scaffold devices - To identify optimal strategies for lesion preparation in cases treated with DCB - To identify possible predictors for TLR after treatment with DCB - To describe early and late angiographic and OCT-findings among coronary artery disease (CAD) patients treated with DCB and/or various metallic stent and scaffold devices - To evaluate the impact of different antithrombotic regimens on patient's clinical outcomes - To study procedural and clinical outcomes among CAD patients requiring hemodynamic support using mechanical devices. - To describe economic implications (cost-effectiveness) of various interventional treatments for CAD. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04988685
Study type Observational [Patient Registry]
Source Luzerner Kantonsspital
Contact Florim Cuculi, MD
Phone +41412052134
Email florim.cuculi@luks.ch
Status Recruiting
Phase
Start date June 1, 2021
Completion date December 31, 2031
View Details
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