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Cutting balloon versus standard balloon for lesion preparation of drug-coated balloon treatment in de-novo coronary artery lesions: Rationale and design of the randomized NATURE trial

  • Masafumi Ono
  • , Taku Asano
  • , Masahiko Noguchi
  • , Norihiro Kogame
  • , Raisuke Iijima
  • , Kohei Osakada
  • , Kenji Ando
  • , Takayuki Ishihara
  • , Koji Nishida
  • , Mamoru Nanasato
  • , Kengo Tanabe
  • , Takashi Muramatsu
  • , Atsunori Okamura
  • , Yoshihisa Kinoshita
  • , Kiyoshi Hibi
  • , Satoru Suwa
  • , Nehiro Kuriyama
  • , Kozo Okada
  • , Gaku Nakazawa
  • , Takashi Ashikaga
  • Yutaka Tadano, Hiroki Shiomi, Masato Nakamura, Akiyoshi Miyazawa, Satoshi Miyata, Kiyoko Uno, Kazushige Kadota, Ken Kozuma

研究成果: ジャーナルへの寄稿学術論文査読

抄録

Background Drug-coated balloons (DCBs) have emerged as an alternative to drug-eluting stents (DESs) for percutaneous coronary intervention (PCI) in de novo coronary artery diseases (CADs). However, the optimal predilatation strategy prior to DCB dilatation has yet to be validated. Methods/design The NATURE ( N on-stent PCI with an a ppropriate dila t ation by means of c u tting balloon and d r ug-coated balloon in de novo l e sion) study is a prospective, multi-center, randomized controlled trial designed to evaluate the safety and efficacy of a cutting balloon compared to standard balloons (semi-compliant or non-compliant balloons) for lesion preparation prior to DCB treatment in normal-sized vessels. The DCB treatment is performed with the guidance of intravascular ultrasound (IVUS) and fractional flow reserve (FFR). The study will enroll 200 patients with a single de novo coronary lesion (reference vessel diameter: 2.5–4.0 mm) at 18 sites. Patients are randomized 1:1 to undergo predilatation with either a cutting or standard balloons, followed by DCB dilatation. The primary endpoint is the success rate of optimal predilatation, as defined by the International DCB Consensus Group: no flow-limiting dissections, residual stenosis ≤30 %, and FFR >0.80. Secondary endpoints include in-segment late lumen loss (LLL) at 9 months, the incidence of bailout stenting, and clinical outcomes at 6 and 12 months. Summary The NATURE study aims to address the critical gap in evidence regarding optimal predilatation for DCBs in de novo CADs. By utilizing state-of-the-art DCB treatment strategies, including cutting balloons, intravascular imaging, and physiological tools, this study is expected to provide meaningful insights for refining DCB-based PCI strategies. Clinical Trial Registration URL: https://jrct.niph.go.jp/ . Unique Identifier: jRCTs032230543.

本文言語英語
ページ(範囲)48-56
ページ数9
ジャーナルCardiovascular Revascularization Medicine
81
DOI
出版ステータス出版済み - 12-2025
外部発表はい

All Science Journal Classification (ASJC) codes

  • 循環器および心血管医学

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