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Artificial Intelligence to Assess the Association Between Facial Characteristics and Coronary Artery Diseases

Artificial Intelligence to Assess the Association Between Facial Characteristics and Coronary Artery Diseases

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03731936
Enrollment
6864
Registered
2018-11-06
Start date
2017-07-10
Completion date
2019-08-02
Last updated
2019-08-20

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

Conditions

Coronary Artery Disease

Keywords

artificial intelligence, facial characteristics

Brief summary

The purposes of this study are 1) to explore the association between facial characteristics and the increased risk of coronary artery diseases; 2) to evaluate the diagnostic efficacy of appearance factors for coronary artery diseases.

Detailed description

Several age-related appearance factors were described associated with increased risk of coronary artery diseases (CAD). However, several limitations made these facial risk factors hard to be utilized in clinical practice, including 1) low prevalence in CAD patients, 2) lack of specific definition, 3) poor reproducibility in artificial recognition. Thus, the investigators designed a multi-center, cross-sectional study to explore the association between facial characteristics and CAD and evaluate the diagnostic efficacy of appearance factors for CAD. The investigators will recruit patients undergoing coronary angiography or coronary computer tomography angiography. Patients' baseline information and facial images will be collected. First, the investigators will explore the facial factors associated with CAD by using artificial intelligence technology to compare facial photographs between patients with CAD and without CAD. Secondary, the investigators will evaluate the dose-response relationship between facial characteristics and CAD. Third, the investigators will establish a CAD risk model based on facial factors, and evaluate the diagnostic effect of the model.

Interventions

OTHERNo intervention

No intervention

Sponsors

China National Center for Cardiovascular Diseases
Lead SponsorOTHER_GOV

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

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

Inclusion criteria

* Undergoing coronary angiography or coronary computer tomography angiography * Written informed consent

Exclusion criteria

* Prior percutaneous coronary intervention (PCI) * Prior coronary artery bypass graft (CABG) * Screening coronary artery disease before treating other heart diseases * Without blood biochemistry outcome * With artificially facial alteration (i.e. cosmetic surgery, facial trauma or make-up) * Other situations which make patients fail to be photographed

Design outcomes

Primary

MeasureTime frameDescription
Sensitivity of diagnostic modelat the end of enrollment (6 months)The sensitivity of coronary artery diagnostic model assessed in model test group

Secondary

MeasureTime frameDescription
Specificity of diagnostic modelat the end of enrollment (6 months)The specificity of coronary artery diagnostic model assessed in model test group
Positive predictive value (PPV)at the end of enrollment (6 months)PPV of diagnostic model assessed in model test group
Negative predictive value (NPV)at the end of enrollment (6 months)NPV of diagnostic model assessed in model test group
Diagnostic accuracy rateat the end of enrollment (6 months)Diagnostic accuracy rate of diagnostic model assessed in model test group

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026