coronary artery disease
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) patients who undertake measurement of FFR 2) patients with stable angina pectoris 3) patients who are over 20 years old when informed consent are collected 4) patients from whom informed consent are collected with adequate understanding of the research
Exclusion criteria
Exclusion criteria: 1) patients who undertake measurement of FFR 2) patients under medical treatments for cerebral hemorrhages in acute phase 3) patients with bronchial asthma 4) patients whom primary investigators or sub investigators decide to exclude because of inadequacies for the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| concordance rate of FFR value measured with pressure wire and FFR value estimated by the software | — |
Secondary
| Measure | Time frame |
|---|---|
| Investigation of influence factors for concordance rate | — |
Countries
Japan
Contacts
The University of Tokyo Hospital Department of Cardiovascular Medicine