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Study identifier: NCT06387693 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Artificial Intelligence in ANOCA

Condition: Angina, Stable  ·  Sponsor: UMC Utrecht

PhaseNA
Planned participants250
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Angina pectoris is diagnosed in \>180.000 people in the Netherlands each year. Diagnosis in angina pectoris focuses on epicardial coronary stenosis, the identification of which may lead to guideline-directed medical therapy or revascularization. However, no such stenosis is identified in 40-70% of patients. This condition, angina with no obstructed coronary artery (ANOCA), is more prevalent in women and is related to poor quality of life, high medical expenses, and a higher incidence of adverse events. The origin of ANOCA can be evaluated during invasive coronary angiography by coronary function testing (CFT) to identify coronary vasomotor disorders. This relates to vasospasm of the coronary artery and microcirculation, or to impaired microvascular vasodilation. For the diagnosis of vasospasm, CFT needs to result in electrocardiographic signs of myocardial ischemia as part of the diagnostic criteria. This is a critical point in the diagnosis of vasospasm, as these signs can be subtle and can vary, and are therefore prone to misinterpretation. Apart from this caveat, the diagnosis approach therefore currently requires an invasive procedure for the diagnosis. This limits the broad application and hampers early identification and treatment of ANOCA. During CFT, a coronary guide wire is routinely advanced in the coronary artery which also allows obtaining an intracoronary ECG by attaching a sterile alligator clamp to a standard electrocardiogram lead. This allows continuous rec…

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

Talk to the study team

Tim P van de Hoef, MD, PhD  ·  +3188755555  ·  t.p.vandehoef@umcutrecht.nl

Always discuss trial participation with your own doctor first.

Locations (1)

UMC UtrechtUtrecht, NetherlandsRecruiting

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Source record: clinicaltrials.gov/study/NCT06387693