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DOI 10.1016/j.ahj.2024.05.004

Медицинская библиотека · American heart journal · 2024

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

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, FLASH Trial Investigators

Протокол клинического исследованияСтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

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.

Для цитирования: 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, FLASH Trial Investigators. Fully automated quantitative coronary angiography versus optical coherence tomography guidance for coronary stent implantation (FLASH): Study protocol for a randomized controlled noninferiority trial.. American heart journal. 2024. DOI: 10.1016/j.ahj.2024.05.004.

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