New-DES vs BMS in SVG -1 Year Outcomes (BALTIC)

Medical University of Silesia

Status: Completed

Conditions: Coronary Artery Disease

Treatments: Device: new-DES; Device: BMS

Study type: Observational

Funder types: Other

Identifiers

NCT04338308

01

Details and patient eligibility

About

Data regarding the efficacy of the percutaneous coronary intervention (PCI) with new-designed drug-eluting stent (new-DES) vs. bare metal stent (BMS) of saphenous vein grafts (SVG) stenosis is scarce. The primary objective was to compare one-year clinical outcomes of PCI in stenosis of SVG using new-DES vs. BMS in a real-world population. We carried out a multi-center registry comparing new-DES with BMS in all consecutive patients undergoing PCI of SVG. The primary composite endpoint was major adverse cardiac and cerebrovascular events (MACCE) at 1 year.

Enrollment: 792 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• patients after CABG with significant SVG stenosis referred for PCI

Exclusion criteria

• patients who had both types of stents implanted in the same procedure
• patients with the old-DES
• patients who had PCI of other vascular territories during the same procedure

Trial design

792 participants in 1 patient group

SVG PCI

Treatment:

Device: new-DES

Device: BMS