Fully automated quantitative coronary angiography versus optical coherence tomography guidance for coronary stent implantation (FLASH): Study protocol for a randomized controlled noninferiority trial
- Authors
- Kim, Yongcheol; Park, Hanbit; Yoon, Hyuck-Jun; Suh, Jon; Kang, Si-Hyuck; Lim, Young-Hyo; Jang, Duck Hyun; Park, Jae Hyoung; Shin, Eun-Seok; Bae, Jang-Whan; Lee, Jang Hoon; Oh, Jun-Hyok; Kang, Do-Yoon; Kweon, Jihoon; Jo, Min-Woo; Park, Duk-Woo; Kim, Young-Hak; Ahn, Jung-Min
- Issue Date
- Sep-2024
- Publisher
- Mosby Inc.
- Citation
- American Heart Journal, v.275, pp 86 - 95
- Pages
- 10
- Indexed
- SCIE
SCOPUS
- Journal Title
- American Heart Journal
- Volume
- 275
- Start Page
- 86
- End Page
- 95
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/195131
- DOI
- 10.1016/j.ahj.2024.05.004
- ISSN
- 0002-8703
1097-6744
- 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.
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