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Study identifier: NCT07020858 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

FAPI Imaging Predicts Adverse Cardiac Events in Chronic Total Occlusion

Condition: Chronic Total Occlusion (CTO) · Chronic Coronary Syndrome  ·  Sponsor: Lin Zhao

PhaseN/A
Planned participants470
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Prospective, observational, single-center cohort study Hypothesis Higher myocardial FAPI uptake in CTO patients predicts a greater incidence of major adverse cardiovascular events (MACE) within 12 months after PCI. FAPI PET/CT imaging is associated with plaque vulnerability features and may serve as a non-invasive marker for fibrotic activity and adverse cardiac remodeling. Inclusion Criteria * Age ≥ 18 years * Presence of at least one untreated chronic total occlusion (CTO) lesion in a major coronary artery (diameter ≥ 2.5 mm, TIMI 0 flow for ≥ 3 months) confirmed by coronary angiography or CTCA * Patient eligible for PCI and undergoing FAPI PET/CT imaging prior to intervention * Written informed consent provided Exclusion Criteria * Allergy or contraindication to antiplatelet agents (aspirin, clopidogrel, or ticagrelor) * Severe liver dysfunction (liver enzymes \>3× upper limit of normal) * Severe chronic kidney disease (eGFR \< 30 mL/min/1.73 m²) * Estimated life expectancy \< 1 year * Pregnancy or potential for pregnancy Primary Endpoint Incidence of 1-year MACE, defined as a composite of: Cardiac death, Myocardial infarction, Stroke, Urgent revascularization Secondary Endpoints * All-Cause Mortality * Death from any cause within 12 months * Quality of Life Change: Measured by Seattle Angina Questionnaire (SAQ): changes in angina frequency, physical limitation, and treatment satisfaction * Repeat PCI Events: Incidence of: In-stent restenosis (ISR): ≥50% luminal lo…

This description comes directly from the study's public registry record.

Talk to the study team

Shengwen Yang, Dr  ·  +8601085231480  ·  verayang1990@163.com

Bin Tu  ·  +8601085231480  ·  dr_bintu@163.com

Always discuss trial participation with your own doctor first.

Locations (1)

Beijing Chaoyang Hospital,Capital Medical University,Beijing,ChinaBeijing, Beijing Municipality, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07020858