Non-Invasive EndoPAT Increases Diagnostic Yield of CAD by Coronary Angiography
Completed
- Conditions
- Coronary Artery Disease
- Registration Number
- NCT01581671
- Lead Sponsor
- Mayo Clinic
- Brief Summary
The purpose of this study is to assess the non-invasive, Peripheral Arterial Tonometry (PAT) testing as another way of predicting potential coronary artery blockages in the heart.
- Detailed Description
We are conducting a 16 minute, non-invasive EndoPAT test on patients coming to our cath lab for a first-time angiogram. The angiogram results will be compared to the EndoPAT results to determine if the EndoPAT test, which generates a score, is successful in predicting who may have blockages in their coronary arteries.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 201
Inclusion Criteria
- Patients without known coronary disease who are referred for coronary angiography.
- Adults 18 years and older.
Read More
Exclusion Criteria
- Patients with known coronary disease, acute coronary syndrome, cardiac transplantation, and severe connective tissue disease.
Read More
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To determine if the assessment of endothelial function by non-invasive peripheral arterial tonometry improves diagnostic yield of elective coronary angiography same day as the angiogram Will compare the score of the EndoPAT test to the outcome of the angiogram to determine if the score is predictive of coronary artery disease.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Mayo Clinic
🇺🇸Rochester, Minnesota, United States