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Completed

NCT Number: NCT03731936

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

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Beijing Anzhen hospital, Beijing, Beijing Municipality, China

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About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

No intervention

Other

No intervention

Primary outcomes

  1. Sensitivity of diagnostic model

    Time frame: at the end of enrollment (6 months)

    The sensitivity of coronary artery diagnostic model assessed in model test group

Secondary outcomes

  1. Specificity of diagnostic model

    Time frame: at the end of enrollment (6 months)

    The specificity of coronary artery diagnostic model assessed in model test group

  2. Specificity of diagnostic model

    Time frame: at the end of enrollment (6 months)

    Area under receiver operating curve (AUC) of diagnostic model assessed in model test group

  3. Positive predictive value (PPV)

    Time frame: at the end of enrollment (6 months)

    PPV of diagnostic model assessed in model test group

  4. Negative predictive value (NPV)

    Time frame: at the end of enrollment (6 months)

    NPV of diagnostic model assessed in model test group

  5. Diagnostic accuracy rate

    Time frame: at the end of enrollment (6 months)

    Diagnostic accuracy rate of diagnostic model assessed in model test group

Sponsors and collaborators

Lead sponsor

China National Center for Cardiovascular Diseases

Other Gov

Registry information

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Nov 6, 2018
Registry last updated
Aug 20, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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