A Case-control Study to Assess the Association Between Facial Characteristics and Coronary Artery Diseases
1 other identifier
observational
2,300
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jul 2017
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 8, 2017
CompletedStudy Start
First participant enrolled
July 10, 2017
CompletedFirst Posted
Study publicly available on registry
July 12, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 31, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
October 31, 2018
CompletedNovember 6, 2018
November 1, 2018
1.3 years
July 8, 2017
November 5, 2018
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
The association between facial factors and increased risk of coronary artery diseases
at the end of enrollment (6 months)
Study Arms (2)
Coronary artery disease (CAD) group
Patients enrolled with at least one coronary lesion stenosis ≥50% according to coronary computer tomography or coronary angiography will be assigned to CAD group.
No CAD group
Patients enrolled without coronary lesion stenosis ≥50% according to coronary computer tomography or coronary angiography will be assigned to CAD group.
Interventions
The exposures are facial characteristics which differ significantly in exposure rates between coronary artery disease (CAD) group and no CAD group.
Eligibility Criteria
Patients who undergo coronary computer tomography or coronary angiography from both resident patients and outpatient.
You may qualify if:
- Undergoing coronary computer tomography or coronary angiography
- Written informed consent
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Fuwai Hospital Chinese Academay of Medical Science and National Center for Cardiovascular Diseases
Beijing, Beijing Municipality, 100037, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER GOV
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 8, 2017
First Posted
July 12, 2017
Study Start
July 10, 2017
Primary Completion
October 31, 2018
Study Completion
October 31, 2018
Last Updated
November 6, 2018
Record last verified: 2018-11