Evidence map›Paper›PMID 42642691›Full record

Trial reportCardiovascular intervention and therapeutics2026

Cutting vs standard balloon for lesion preparation in drug-coated balloon-only PCI: the NATURE randomised trial.

Taku Asano, Masafumi Ono, Norihiro Kogame, Masahiko Noguchi, Mitsuaki Sawano, Raisuke Iijima, Kohei Osakada, Takayuki Ishihara, Koji Nishida, Kenji Ando and 16 more

Abstract readRandomized Controlled TrialMulticenter Study
In one paragraph

Trial report in Cardiovascular intervention and therapeutics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

26 authors.

Taku AsanoDepartment of Cardiology, St. Luke's International Hospital, 9-1 Akashi-Cho, Chuo-Ku, P.O. Box 104-8560, Tokyo, Japan. ta.brilliantsea@gmail.com.ORCID https://orcid.org/0000-0001-5733-3381
Masafumi OnoDepartment of Cardiology, St. Luke's International Hospital, 9-1 Akashi-Cho, Chuo-Ku, P.O. Box 104-8560, Tokyo, Japan.
Norihiro KogameDepartment of Cardiology, Tokyo Rosai Hospital, Tokyo, Japan.
Masahiko NoguchiDepartment of Cardiology, Tokyo Bay Urayasu Ichikawa Medical Centre, Chiba, Japan.
Mitsuaki SawanoTeikyo Academic Research Center, Teikyo University, Tokyo, Japan.
Raisuke IijimaDivision of Cardiovascular Medicine, Toho University Ohashi Medical Centre, Tokyo, Japan.
Kohei OsakadaDepartment of Cardiovascular Medicine, Kurashiki Central Hospital, Kurashiki, Okayama, Japan.
Takayuki IshiharaKansai Rosai Hospital Cardiovascular Centre, Hyogo, Japan.
Koji NishidaDepartment of Cardiology, Chikamori Hospital, Kochi, Japan.
Kenji AndoDepartment of Cardiology, Kokura Memorial Hospital, Fukuoka, Japan.
Mamoru NanasatoDepartment of Cardiology, Sakakibara Heart Institute, Tokyo, Japan.
Takashi AshikagaDepartment of Cardiology, Japanese Red Cross Musashino Hospital, Tokyo, Japan.
Kengo TanabeDivision of Cardiology, Mitsui Memorial Hospital, Tokyo, Japan.
Takashi MuramatsuDepartment of Cardiology, Fujita Health University Hospital, Aichi, Japan.
Kiyoshi HibiDepartment of Cardiology, Yokohama City University Hospital, Kanagawa, Japan.
Atsunori OkamuraCardiovascular Centre, Sakurabashi Watanabe Advanced Healthcare Hospital, Osaka, Japan.
Yoshihisa KinoshitaDepartment of Cardiology, Toyohashi Heart Centre, Toyohashi, Aichi, Japan.
Satoru SuwaDepartment of Cardiology, Juntendo University Shizuoka Hospital, Shizuoka, Japan.
Kozo OkadaDivision of Cardiology, Yokohama City University Medical Centre, Kanagawa, Japan.
Nehiro KuriyamaCardiovascular Centre, Miyazaki Medical Association Hospital, Miyazaki, Japan.
Gaku NakazawaDepartment of Cardiology, Faculty of Medicine, Kindai University, Osaka, Japan.
Masato NakamuraDivision of Minimally Invasive Treatment in Cardiovascular Medicine, Toho University Ohashi Medical Centre, Tokyo, Japan.
Satoshi MiyataGraduate School of Public Health, Teikyo University School of Medicine, Tokyo, Japan.
Kazushige KadotaDepartment of Cardiovascular Medicine, Kurashiki Central Hospital, Kurashiki, Okayama, Japan.
Ken KozumaDivision of Cardiology, Department of Internal Medicine, Teikyo University School of Medicine, Tokyo, Japan.
NATURE trial investigators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The success of drug-coated balloon (DCB) therapy for de novo coronary lesions relies on optimal lesion preparation. However, evidence supporting the use of cutting balloons (CBs) for lesion preparation in DCB-only strategies remains limited. The NATURE trial assessed the effectiveness of CB compared with standard balloon (SB) predilatation in achieving optimal lesion preparation for a DCB-only strategy. The NATURE trial was a prospective, multicentre, randomised study conducted at 19 Japanese centres. Patients with de novo coronary lesions suitable for a DCB-only strategy were randomised (1:1) to lesion preparation with CB or SB. Post-predilatation assessment included coronary angiography, intravascular ultrasound (IVUS), and fractional flow reserve (FFR). The primary endpoint was optimal lesion preparation, defined as the simultaneous presence of: (1) no flow-limiting dissection, (2) residual diameter stenosis ≤ 30% by quantitative coronary angiography, and (3) FFR > 0.80. Among 201 patients included in the intention-to-treat population, optimal lesion preparation was achieved in 35.6% of the CB group and 30.0% of the SB group (adjusted risk ratio 1.19, 95% confidence interval 0.87-1.65; p = 0.28). Avoidance of flow-limiting dissection was high in both groups (98.0% vs 97.0%). CB predilatation resulted in lower residual diameter stenosis (30.8 ± 11.8% vs 34.5 ± 13.3%; p = 0.04) and less acute recoil (1.18 ± 0.36 vs 1.31 ± 0.50 mm; p = 0.03). Trends towards larger lumen dimensions on IVUS were also observed with CB. In patients undergoing DCB-only PCI for de novo coronary lesions, CB predilatation provided modest angiographic advantages compared with SB but did not significantly increase the rate of optimal lesion preparation. Optimal lesion preparation is essential for successful drug-coated balloon (DCB) therapy because DCBs do not provide mechanical scaffolding to maintain vessel patency. In this multicentre randomised trial, cutting balloon predilatation resulted in greater acute luminal expansion and less recoil than standard balloon predilatation, although it did not significantly increase the overall rate of optimal lesion preparation defined by angiographic and physiological criteria. These findings suggest that cutting balloons may offer modest mechanical advantages during lesion preparation in DCB-only PCI. However, the clinical significance of these acute angiographic advantages requires confirmation in larger trials and through longer-term follow-up.

Indexed as

Angioplasty, Balloon, CoronaryCoronary Artery DiseaseCoronary StenosisCoronary VesselsAgedCoronary AngiographyFemaleFractional Flow Reserve, MyocardialHumansJapanMaleMiddle AgedProspective StudiesTreatment OutcomeUltrasonography, InterventionalCutting balloonDe novo coronary artery diseaseDrug-coated balloonFractional flow reserveIntravascular ultrasoundLesion preparation

Identifiers

PMID42642691
PMCPMC13582048

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.