Prognostic Implications of AccuFFRangio-guided PCI in STEMI
- Conditions
- Coronary Artery DiseaseST Elevation Myocardial Infarction
- Registration Number
- NCT05209503
- Lead Sponsor
- Wuhan Asia Heart Hospital
- Brief Summary
This is a prospective, single-center clinical trial. AccuFFRangio (ArteryFlow Technology Co., Ltd., Hangzhou, China) is a novel method for evaluating the functional significance of coronary stenosis by computing the pressure in the vessel based on angiographic images. The aim of this study was to evaluate the diagnostic accuracy and prognostic implications of AccuFFRangio in patients with ST-segment elevation myocardial infarction (STEMI).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 500
- 18 Years and older
- STEMI patients with primary percutaneous coronary intervention within 24 hours with at least 1 non-IRA
- Diameter stenosis of 50%-90% by visual estimate
- Reference vessel size > 2 mm in stenotic segment by visual estimate
- LVEF ≤ 40%
- eGFR < 60 mL/min
- Allergy to contrast media, adenosine
- Prior CABG
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Vessel-oriented composite endpoints (VOCEs) 1 year Composite of vessel-related cardiovascular death, vessel-related myocardial infarction, and ischemia-driven target vessel revascularization.
Post-PCI AccuFFRangio 1 year AccuFFRangio limits to yield no VOCEs (Composite of vessel-related cardiovascular death, vessel-related myocardial).
- Secondary Outcome Measures
Name Time Method Cost analysis 1 year Cost savings of AccuFFRangio-guided strategy. Evaluation of costs by excess/reduced need for PCI when AccuFFRangio and Angiography disagree.
Prognostic implications 1 year The time from randomization to first occurrence of any of composite outcome including vessel-related cardiovascular death, vessel-related myocardial infarction, and ischemia-driven target vessel revascularization.
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