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A Case-control Study to Assess the Association Between Facial Characteristics and Coronary Artery Diseases

N

National Center for Cardiovascular Diseases

Status

Completed

Conditions

Coronary Artery Disease

Treatments

Other: Facial characteristics

Study type

Observational

Funder types

Other

Identifiers

NCT03214783
2017-907

Details and patient eligibility

About

The purpose of this study is to explore the facial characteristics associated with the increased risk of coronary artery diseases. The secondary purpose is to evaluate the diagnostic efficacy of appearance factors for coronary artery diseases.

Full 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, we designed a case-control study to explore new, common and well-defined facial characteristics associated with CAD and evaluate the diagnostic efficacy of appearence factors in CAD. We will recuit 1150 patients with at least one coronary lesion stenosis ≥50% according to coronary angiography or coronary computer tomography (CAD group) and 1150 patients without coronary lesion stenosis≥ 50% (No CAD group) judged by coronary angiography or coronary computer tomography. We will collect patients' baseline information and facial images. One hand, we will explore the facial factors associated with CAD by comparing the exposure rates of different facial factors in CAD group and No CAD group based on artificial intelligence technology. On the other hand, we will build a CAD risk model based on facial factors, and evaluate the diagnostic effect of the model.

Enrollment

2,300 patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

  • Prior percutaneous coronary intervention (PCI)
  • Prior coronary artery bypass graft (CABG)
  • 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

Trial design

2,300 participants in 2 patient groups

Coronary artery disease (CAD) group
Description:
Patients enrolled with at least one coronary lesion stenosis ≥50% according to coronary computer tomography or coronary angiography will be assigned to CAD group.
Treatment:
Other: Facial characteristics
No CAD group
Description:
Patients enrolled without coronary lesion stenosis ≥50% according to coronary computer tomography or coronary angiography will be assigned to CAD group.
Treatment:
Other: Facial characteristics

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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