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Study identifier: NCT07151976 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Thrombus Aspiration and Pathology and OCT Study

Condition: Acute Coronary Syndrome  ·  Sponsor: Fujita Health University

PhaseN/A
Planned participants200
Who can joinAll sexes, 20 Years to no upper limit
Healthy volunteersNo

About this study

Most acute coronary syndromes (ACS) are caused by plaque complications triggering thrombotic events in the culprit plaques. Plaque complications include plaque rupture (Ruptured Fibrous Cap-RFC) with exposure of highly thrombogenic substrate to the flow and plaque erosion (Intact Fibrous Cap-IFC) a condition characterized by endothelial/intimal damage occurring over non-ruptured plaques. Far less commonly (\<5%), calcified nodules (CN) may trigger acute coronary thrombosis. Plaque rupture accounts for 75% of fatal AMI in autopsy series, while erosion is found in about 25% of cases. These proportions have been supported by in vivo invasive studies (OCT) and OCT-pathology correlation studies. However, it remains unclear whether OCT findings consistently align with in vivo pathology-based evidence of RFC in ACS. Guidelines addressing treatments of ACS unanimously indicate percutaneous coronary intervention (PCI) to restore the coronary flow. Pre-PCI thrombus aspiration is not currently indicated by most guidelines, with the exception of cases with very high thrombus burden. The samples retrieved from thrombus aspiration can be suitable for pathology investigation and aim to evaluate the presence of plaque components in the context of the thrombotic material, a finding that demonstrates plaque rupture as the substrate for the acute coronary event. These studies are uniquely qualified to provide information on the correct OCT-based interpretation of plaque complications in ACS and…

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

Talk to the study team

Yukio Ozaki, MD, PhD  ·  +1 9492996512  ·  ozakiyuk@fujita-hu.ac.jp

Reina Ozaki, MD  ·  +1 9492996512  ·  yukio.ozaki7@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Fujita Health UniversityToyoake, Aichi-ken, JapanRecruiting

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Source record: clinicaltrials.gov/study/NCT07151976