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CCTA Improves Clinical Management of Stable Chest Pain

Improving the Clinical Management of Stable Chest Pain Based on Imaging: a Registry of Computed Tomography Coronary Angiography

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04691037
Acronym
CICM-SCP
Enrollment
50000
Registered
2020-12-31
Start date
2016-01-01
Completion date
2030-01-01
Last updated
2024-03-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Disease, Coronary Computed Tomography Angiography, Invasive Coronary Angiography, Major Adverse Cardiovascular Events, Optimal Medical Therapy, Revascularization, Stable Chest Pain

Brief summary

The investigator aims to prospectively enroll patients who were referred for coronary computed tomography angiography (CCTA) for the assessment of stable chest pain (SCP) suspected of obstructive coronary artery disease (CAD). All patients underwent CCTA according to established guidelines and local institutional protocols. The imaging data were evaluated using different image post-processing software to comprehensively analyse anatomical, functional and histological information of coronary. This study will determine if CCTA-based imaging evaluation can provide more informaton to improve clinical management for SCP, including fewer MACE and better decision-making of downstream investigations and therapeutic interventions.

Interventions

DIAGNOSTIC_TESTCCTA

All patients underwent CCTA according to established guidelines and local institutional protocols. The imaging data were evaluated using different image post-processing software to comprehensively analyse anatomical, functional and histological information of coronary.

Sponsors

Tianjin Chest Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* symptomatic patients with SCP suspected of obstructive CAD. * referred for CCTA for the assessment of SCP. * ≥18 years of age. * signed informed consent.

Exclusion criteria

* acute coronary syndromes * previous CAD or coronary revascularization * nonsinus rhythm * cardiomyopathy, valvular disease, congenital heart disease or left cardiac insufficiency because of other reasons

Design outcomes

Primary

MeasureTime frameDescription
Major adverse cardiovascular events10 yearsCardiac death and myocardial infarction

Secondary

MeasureTime frameDescription
Medication prescription10 yearsChange for medication prescription of antiplatelet agents, anti-ischemic drugs, lipid-lowering agents, angiotensin-converting enzyme inhibition and so on, attributed to CCTA results or unplanned,
Coronary revascularization10 yearsPTCA, PCI or CABG occurred at follow-up after CCTA, attributed to CCTA results or unplanned.
Number of Participants with Death10 years
Invasive coronary angiography10 yearsInvasive coronary angiography occurred at follow-up after CCTA, attributed to CCTA results or unplanned.
Number of Participants with Cardiac death10 years
Number of Participants with Myocardial infarction10 years
Number of Participants with Stroke3 years

Countries

China

Contacts

Primary ContactJia Zhou
zhoujiawenzhang@126.com+8615522485560

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026