Coronary Occlusion Clinical Trial
Official title:
Functional Assessment-guided Angioplasty in Patients With Coronary Chronic Total Occlusion (FAGA-CTO)
The aim of this study is to investigate the role of functional evaluation for predicting clinical outcome in patients with coronary chronic total occlusion (CTO) undergoing percutaneous coronary intervention (PCI), and to evaluate the clinical evidence for the using of fractional flow reserve (FFR), coronary flow reserve (CFR), index of myocardial resistance (IMR) and dynamic single photon emission computed tomography (D-SPECT) in these patients.
PCI for CTO has dramatically changed in recent years. Although, with the improvement of
devices and refinement of operator techniques, PCI of CTO can currently be performed with
high success and low complication rates at experienced centers, the clinical benefit of
recanalization of CTO is still a matter of debate. Accumulating evidence suggests that the
improvement of left ventricular functional and prognosis is closely related with the area of
viable myocardium, which has the potential for contractile recovery after revascularization.
For the majority of interventional cardiologists, coronary angiography is the only invasive
test deemed necessary for clinical decision-making, despite its weak ability to predict the
functional impact of vascular occlusion on the subtended myocardium. To overcome this
limitation, adjunctive diagnostic tools for functional evaluation, such as FFR, CFR, IMR and
D-SPECT, have been introduced. In non-CTO patients, physiology-guided revascularization
strategy has been definitely proven to be better than angiography-guided strategy in pivotal
landmark studies. However, the clinical value of these functional parameters for the PCI of
CTO is still unknown.
The aim of this study was to determine whether functional evaluation is a better predictor of
clinical outcome in patients with CTO undergoing PCI.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT01721096 -
XIENCE PRIME Japan Post-Marketing Surveillance (PMS)
|
||
Completed |
NCT00987610 -
Guidewire for Chronic Total Occlusion
|
Phase 4 | |
Completed |
NCT02533128 -
Biomarkers, Blood Pressure, BIS: Risk Stratification/Management of Patients at Cardiac Risk in Major Noncardiac Surgery
|
N/A | |
Completed |
NCT04246125 -
Patient Skin Dose in Interventional Radiology
|
||
Completed |
NCT03717675 -
Supplemental Study to Evaluate the Safety and Effectiveness of the NovaCross™ Micro-catheter
|
N/A | |
Recruiting |
NCT03588481 -
IRIS- DESyne X2 in the IRIS-DES Registry
|
||
Recruiting |
NCT05089864 -
STAR and Deferred Stenting Study
|
N/A | |
Not yet recruiting |
NCT03719014 -
Cohort B of the Pivotal Study to Evaluate the Safety and Effectiveness of the NovaCross™ Micro-catheter
|
N/A | |
Not yet recruiting |
NCT02963584 -
Decision Aid in Chronic Total Occlusion (CTO) Patients
|
N/A | |
Completed |
NCT00793221 -
Non-acute Coronary occlusIon Treated By Everolimus ELuting Stent
|
Phase 3 | |
Completed |
NCT04281212 -
Observational Study Evaluating the Management of Chronic Coronary Occlusions In France
|
||
Not yet recruiting |
NCT04562142 -
A Novel Non-Invasive Acoustic Diagnostic for the Diagnosis of Coronary Artery Disease The CAD-det Validation Study
|
N/A | |
Enrolling by invitation |
NCT02931331 -
Coronary Revascularization Assessed by Stress PET
|
N/A | |
Terminated |
NCT02683356 -
Optical Coherence Tomography to Improve Outcome for Coronary Revascularisation Using Bioresorbable Vascular Scaffolds
|
N/A | |
Completed |
NCT00657436 -
Myeloid-Related Protein in Evaluation of Acute Chest Pain in the Emergency Departement
|
N/A | |
Not yet recruiting |
NCT05848232 -
Single-Arm Study Evaluating Use of the CORA Catheters for the Crossing of Coronary Chronic Total Occlusions
|
Phase 3 | |
Terminated |
NCT03993522 -
Exercise in Patients With a Total Coronary Occlusion
|
N/A | |
Not yet recruiting |
NCT03159650 -
Comparative Study Between Intravascular Ultrasonography Guided and Angiography-guided Recanalization of Coronary Chronic Total Occlusions
|
N/A | |
Recruiting |
NCT02325869 -
Clinical Study Protocol - Debris Interventional Removal in ACS (DESIRE-ACS)
|
N/A | |
Completed |
NCT00640068 -
Advanced Cardiovascular Imaging Consortium
|
N/A |