Medipixel XA-Assisted PCI in Coronary Artery Disease

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age19+
SponsorCHA University

About this trial

This prospective, multicenter, single-arm, interventional study evaluates the effectiveness and safety of Medipixel XA-Assisted Percutaneous Coronary Intervention (MPXA-PCI) in patients with coronary artery disease (CAD). The study aims to assess procedural success rates and clinical outcomes associated with the novel MPXA-assisted PCI strategy in a real-world clinical setting.

A total of 830 patients with de novo coronary lesions eligible for drug-eluting stent (DES) implantation will be enrolled. All participants will undergo MPXA-assisted lesion assessment to optimize balloon and stent selection. The primary outcome is target vessel failure (TVF) at 12 months, defined as a composite of cardiac death, target vessel-related myocardial infarction, and clinically driven target vessel revascularization. Secondary outcomes include procedural success, angiographic results, and periprocedural complications.

This study will provide evidence regarding the clinical applicability and safety of artificial intelligence-assisted quantitative coronary analysis (AI-QCA) technology for optimizing PCI procedures.

Eligibility criteria

Qualifiers

Silent ischemia, stable or unstable angina, or myocardial infarction

De novo coronary lesion eligible for DES implantation

Lesions analyzable by MPXA

Disqualifiers

Comorbidity with a life expectancy <12 months

Intolerant of antithrombotic therapy

Significant anemia, thrombocytopenia, or leucopenia

History of major hemorrhage (intracranial, gastrointestinal, and so on)

Trial design

Treatments tested in this trial

  • Medipixel XA-Assisted Percutaneous Coronary Intervention

Treatment groups

830 Participants
are divided into 1 treatment group

Sponsors and collaborators