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Fully automated quantitative coronary angiography versus optical coherence tomography guidance for coronary stent implantation (FLASH): Study protocol for a randomized controlled noninferiority trial

Authors
 Yongcheol Kim  ;  Hanbit Park  ;  Hyuck-Jun Yoon  ;  Jon Suh  ;  Si-Hyuck Kang  ;  Young-Hyo Lim  ;  Duck Hyun Jang  ;  Jae Hyoung Park  ;  Eun-Seok Shin  ;  Jang-Whan Bae  ;  Jang Hoon Lee  ;  Jun-Hyok Oh  ;  Do-Yoon Kang  ;  Jihoon Kweon  ;  Min-Woo Jo  ;  Duk-Woo Park  ;  Young-Hak Kim  ;  Jung-Min Ahn  ;  FLASH Trial Investigators 
Citation
 AMERICAN HEART JOURNAL, Vol.275 : 86-95, 2024-05 
Journal Title
AMERICAN HEART JOURNAL
ISSN
 0002-8703 
Issue Date
2024-05
Abstract
Background: Artificial intelligence-based quantitative coronary angiography (AI-QCA) has been developed to provide a more objective and reproducible data about the severity of coronary artery stenosis and the dimensions of the vessel for intervention in real-time, overcoming the limitations of significant inter- and intraobserver variability, and time-consuming nature of on-site QCA, without requiring extra time and effort. Compared with the subjective nature of visually estimated conventional CAG guidance, AI-QCA guidance provides a more practical and standardized angiography-based approach. Although the advantage of intravascular imaging-guided PCI is increasingly recognized, their broader adoption is limited by clinical and economic barriers in many catheterization laboratories.

Methods: The FLASH (fully automated quantitative coronary angiography versus optical coherence tomography guidance for coronary stent implantation) trial is a randomized, investigator-initiated, multicenter, open-label, noninferiority trial comparing the AI-QCA-assisted PCI strategy with optical coherence tomography-guided PCI strategy in patients with significant coronary artery disease. All operators will utilize a novel, standardized AI-QCA software and PCI protocol in the AI-QCA-assisted group. A total of 400 patients will be randomized to either group at a 1:1 ratio. The primary endpoint is the minimal stent area (mm2), determined by the final OCT run after completion of PCI. Clinical follow-up and cost-effectiveness evaluations are planned at 1 month and 6 months for all patients enrolled in the study.

Results: Enrollment of a total of 400 patients from the 13 participating centers in South Korea will be completed in February 2024. Follow-up of the last enrolled patients will be completed in August 2024, and primary results will be available by late 2024.

Conclusion: The FLASH is the first clinical trial to evaluate the feasibility of AI-QCA-assisted PCI, and will provide the clinical evidence on AI-QCA assistance in the field of coronary intervention.

Clinical trial registration: URL: https://www.

Clinicaltrials: gov. Unique identifier: NCT05388357.
Full Text
https://www.sciencedirect.com/science/article/pii/S0002870324001194
DOI
10.1016/j.ahj.2024.05.004
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Yongcheol(김용철) ORCID logo https://orcid.org/0000-0001-5568-4161
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/200224
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