Predictive Role of Photon Counting Computed Tomography in Acute Coronary Syndrom Patients

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorChinese PLA General Hospital

About this trial

For patients with severe calcification or complex non-calcified plaques, we investigate wether PCCT can enable non-invasive, in vivo precise differentiation and quantitative measurement of plaque components (e.g., spotty calcification, necrotic core, fibrous tissue). Further we also study wether these quantitative imaging features can independently predict the risk of MACE in the short term and long term

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adult patients (≥18 years) with clinically diagnosed coronary artery disease or undergoing CCTA for chest pain/heart failure symptoms.

Able and willing to provide informed consent and complete scheduled follow-up visits.

Disqualifiers

History of iodine contrast agent allergy.

Severe renal insufficiency (eGFR < 30 mL/min/1.73 m²).

History of prior coronary artery bypass grafting (CABG).

Pregnant or lactating women

Trial population

coronary artery disease patients referred to photon-counting CT examination

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • there is no intervention in this study

    Other intervention

    there is no intervention

Treatment groups

180 Participants
are divided into 1 treatment group
Group A: coronary artery disease patients referred to photon-counting CT examination1 intervention

Trial outcomes

Primary outcomes

1

Major Adverse Cardiovascular Events, MACE

Non-fatal myocardial infarction Non-fatal stroke Cardiovascular death Revascularization Acute heart failure

Time frame
12months

Secondary outcomes

Other outcomes

Sponsors and contacts

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