Coronary Occlusion

5

Review clinical trials related to Coronary Occlusion. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

IRIS- DESyne X2 in the IRIS-DES Registry

This study evaluates effectiveness and safety of DESyne X2 in Routine Clinical Practice.

Participants needed: 1,000
Trial details
Age: 19+Biological sex: AllType: ObservationalSponsor: Seung-Jung ParkUpdated: Jun 24, 2026Locations: 6
Eligibility criteria

Age 19 and more [+2]

Intervention with DeSyne X2 drug-eluting coronary stent and other drug eluting s... [+2]

Status: Recruiting

Polish Registry of Percutaneous Coronary Intervention for Chronic Total Occlusions

The goal of this observational study is to evaluate the safety, efficacy, and clinical outcomes of percutaneous coronary intervention (PCI) for chronic total occlusions (CTO) in patients treated in contemporary clinical practice in Poland. The main questions it aims to answer are: * What are the rates of procedural success and periprocedural complications of CTO PCI in routine clinical practice? * How do CTO PCI strategies and techniques, intravascular imaging, different treatment strategies, and mechanical circulatory support affect clinical outcomes? * How do clinical outcomes differ among different patient subgroups? * Can artificial intelligence-based analysis predict clinical and quality-of-life outcomes after CTO PCI? Patients undergoing CTO PCI as part of their standard medical care will be prospectively enrolled in a national, multicenter registry, with clinical, procedural, and follow-up data collected to evaluate real-world outcomes.

Participants needed: 1,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: National Institute of Cardiology, Warsaw, PolandUpdated: Jan 9, 2026Locations: 21Duration: 1 Year
Eligibility criteria

Patients undergoing CTO PCI based on clinical grounds

Age <18 years [+1]

Status: Recruiting

Antegrade Dissection and Re-entry Versus Retrograde Strategy in CTO PCI

The ADRENALINE trial has been designed as a multi-center, prospective randomized study to compare the procedural and periprocedural outcomes of coronary chronic total occlusion (CTO) percutaneous coronary intervention (PCI) using antegrade dissection and re-entry (ADR) versus retrograde strategy. Beyond the patient-oriented outcomes, the influence of the studied CTO PCI strategies on the stress levels among interventional cardiologists will be explored. The main questions it aims to answer are as follows: * What is the difference between ADR versus retrograde strategy with regard to total procedure time, the rates of successful guidewire crossing and periprocedural complications as well as stress levels experienced by interventional cardiologists? * Is retrograde approach associated with higher rates of myocardial injury/infarction based on cardiac troponin/cardiac magnetic resonance (CMR) as compared with ADR? Participants will undergo pre- and postprocedural laboratory testing (cardiac troponin, CK-MB), CMR for late gadolinium enhancement and health status assessment. Subjects undergoing successful CTO PCI using antegrade wiring strategy will be included in the observational arm.

Participants needed: 74
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: National Institute of Cardiology, Warsaw, PolandUpdated: Jan 2, 2026Locations: 3
Eligibility criteria

clinical indication for CTO PCI as determined by the local heart team (presence... [+3]

<18 years of age [+9]

Status: Not yet recruiting

A MAajor RAdiation-based PCI Study in STEMI and NSTEMI

In France and Italy, approximately 240,000 percutaneous coronary angioplasties (PCI) are performed annually, with an increasing number of complex procedures, including those involving the left coronary common trunk, a bifurcation, chronic occlusion, or requiring Rotablator Rotary Atherectomy (ARota). The medical literature lacks sufficient data regarding several key aspects of complex angioplasty. These include the epidemiological characteristics of patients undergoing such procedures, the impact of irradiation delivered and the quantity of iodine injected on these lengthy procedures, their procedural complication rate, and in-hospital mortality.

Participants needed: 15,630
Trial details
Age: 18-90Biological sex: AllType: ObservationalSponsor: Centre Cardiologique du NordUpdated: Dec 27, 2024Duration: 5 Years
Eligibility criteria

The patient presents with a STEMI or NSTEMI requiring either a non-complex or co...

Status: Recruiting

PBM as Strategy to CABG Anemic Patients Bypass Graft (CABG)

Anemia poses risks during coronary artery bypass grafting (CABG), increasing complications and mortality rates. Blood transfusions in cardiac surgery have negative outcomes, prompting the use of erythropoietin in Patient Blood Management (PBM) to limit transfusion needs and enhance postoperative recovery. EPO can reduce blood component requirements, adverse events, and inflammation in anemic CABG patients. A study aims to minimize transfusions through a PBM anemia treatment protocol for CABG patients, comparing outcomes in three groups: a Control Group (CG), a Non-PBM Group (NPBMG) treated with blood components, and a PBM Group (GPBM) treated with EPO. Parameters include post-op stay, mortality, cardiovascular events, non-cardiovascular events, ICU time, mechanical ventilation duration, vasoactive drug use, inflammatory responses, and cardiac cell death. Analysis will consider demographic and clinical factors, with expectations that GPBM will yield superior results compared to NPBMG and similar or better outcomes than CG.

Participants needed: 120
Trial details
Phase: Phase 2Age: 18-80Biological sex: AllType: InterventionalSponsor: Federal University of São PauloUpdated: Aug 7, 2024Locations: 1
Eligibility criteria

Eletive surgery; [+2]

Age > 80 years; [+13]