|D003327||Coronary Disease NIH||0.38|
|D003324||Coronary Artery Disease NIH||0.38|
There is one clinical trial.
The overall purpose of the FAVOR III China trial is to investigate if a strategy of quantitative flow ratio (QFR)-guided percutaneous coronary intervention (PCI) yields superior clinical outcome and cost-effectiveness compared to a strategy of standard coronary angiography-guided PCI in evaluation of patients with coronary artery disease.
Description: A composite of all-cause mortality, any myocardial infarction and any ischemia-driven revascularizationMeasure: MACE Time: 1 year
Description: all-cause mortality, any spontaneous myocardial infarction and any ischemia-driven revascularizationMeasure: MACE excluding peri-procedural MI (Major secondary endpoint) Time: 1 year
Description: Cardiovascular, non-cardiovascular and undetermined deathMeasure: Death Time: 1 month, 6 months, 1 year, 2 years and 3 years
Description: Target vessel related and non-target vessel related MIMeasure: MI Time: 1 month, 6 months, 1 year, 2 years and 3 years
Description: The ischemia driven and non-ischemia driven TVRMeasure: Target vessel revascularization (TVR) Time: 1 month, 6 months, 1 year, 2 years and 3 years
Description: The The ischemia driven and non-ischemia driven RevascularizationMeasure: Any coronary artery revascularization Time: 1 month, 6 months, 1 year, 2 years and 3 years
Description: Definite and probable stent thrombosis during acute, sub-acute, late, and very late phase according to the Academic Research Consortium (ARC)-2Measure: Definite or probable stent thrombosis Time: 1 month, 6 months, 1 year, 2 years and 3 years
Description: PCI strategy changes following QFR and three-dimension quantitative coronary angiography (3D-QCA)Measure: The PCI strategy changes based on the QFR and 3D-QCA Time: During the procedure
Description: Costs include direct clinical costs during the initial hospitalization and other resources used, main cardiovascular medication expenses, and outpatient and/or hospitalization expenses associated with MACE.Measure: Cost during 1-year follow-up Time: 1 month, 6 months, 1 year
Description: QALYs determined using EuroQol five dimensions questionnaire (EQ-5D) in official Chinese version, to assess the quality of life.Measure: Quality-adjusted-life-years (QALYs) index Time: 1 month, 6 months, 1 year
Data processed on September 26, 2020.
An HTML report was created for each of the unique drugs, MeSH, and HPO terms associated with COVID-19 clinical trials. Each report contains a list of either the drug, the MeSH terms, or the HPO terms. All of the terms in a category are displayed on the left-hand side of the report to enable easy navigation, and the reports contain a list of correlated drugs, MeSH, and HPO terms. Further, all reports contain the details of the clinical trials in which the term is referenced. Every clinical trial report shows the mapped HPO and MeSH terms, which are also hyperlinked. Related HPO terms, with their associated genes, protein mutations, and SNPs are also referenced in the report.Drug Reports MeSH Reports HPO Reports