Stable coronary diseases
Conditions
Interventions
The group (iFR group) which measured predictive value and post PCI value by iFR
The group (RFR group) which measured predictive value and post PCI value by RFR
The group (dPR group) which measured pre
Sponsors
Gifu Heart Center
Toyohashi Heart Center. Nagoya Heart Center
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patient who is scheduled to undergo CAG and iFR, RFR or dPR is positive (0.89 or less) and PCI is planned
Exclusion criteria
Exclusion criteria: Bypass patients. ATP, nicorandil, papaverin contraindicated patients. STEMI. TIMI flow grade <3.90% < stenosis
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Evaluation of the difference and correlation between predictive value of iFR, RFR and dPR; average predictive value and post PCI value of iFR, RFR and dPR | — |
Secondary
| Measure | Time frame |
|---|---|
| 1) Evaluate separately by Type A, B, C (tandem lesion, diffuse lesion) 2) Comparison of measurement time of RFR and dPR compared to iFR 3) Drift of each pressure wire 4) Proportion of 0.9 or more for post iFR, post RFR and post dPR; whether additional treatment was done 5) Whether post FFR achieves 0.8 or more. Whether additional treatment was done 6) Evaluation of plaque properties with IVUS (Terumo,Boston,NIPRO) of fiber component, lipid component, calcification. In particular, the predictive value when highly calcified at least 270 degrees of calcification is observed is not significantly different from the post PCI value. 7) Number of stents used and stent length | — |
Countries
Japan
Contacts
Public ContactHiroyuki Omori
Gifu Heart Center Department of Cardiovascular Medicine
Outcome results
None listed