Sakane, Naoki https://orcid.org/0000-0002-2625-571X
Matsuhisa, Munehide
Kuroda, Akio
Miura, Junnosuke
Hirota, Yushi
Kato, Ken
Toyoda, Masao
Kouyama, Ryuji
Kouyama, Kunichi
Shimada, Akira
Kawashima, Satoshi
Matoba, Yuka
Meguro, Shu
Kusunoki, Yoshiki
Hida, Kazuyuki
Tanaka, Tsuyoshi
Domichi, Masayuki
Suganuma, Akiko
Suzuki, Shota
Tone, Atsuhito
Hosoda, Kiminori
Murata, Takashi
,
Funding for this research was provided by:
Agency for Medical Research and Development (18ek0210104h0001, 19ek0210104h0002, 20ek0210104h0003)
Japan IDDM network (not available)
Article History
Received: 15 March 2023
Accepted: 10 September 2024
First Online: 16 October 2024
Declarations
:
: AS received lecture fees from Terumo and Abbott. SM received lecture fees from Novo Nordisc, Eli Lilly and Boehringer Ingelheim. AT received lecture fees from Eli Lilly, Abbott, Sanofi and Terumo. AK received lecture fees from Eli Lilly. JM received lecture fees from Terumo. YH received lecture fees from Eli Lilly, Sanofi, Abbott, Terumo and Sumitomo Pharma, and research expenses and grants from Sumitomo Pharma. MT received lecture fees from Abbott, Eli Lilly, Sumitomo Pharma, Novo Nordisc and Boehringer Ingelheim and subsides or donations from Cocokara fine Healthcare Inc, LifeScan Japan, Roche DC Japan, SUPER LIGHT WATER CO., LTD. TT received lecture fees from Eli Lilly, and research expenses and grants from AstraZeneca.
: This study conformed to the standards of the Declaration of Helsinki.
: This study is registered in the Japan Registry of Clinical Trials (jRCT1052180075). The study protocol received Certified Review Board (CRB) approval from National Hospital Organization Osaka National Hospital (N2018002, originally approved on February 14, 2019, Version 0.7; the latest revision was approved on May 26, 2020, Version 1.6).
: Informed consent or substitute for it was obtained from all the patients for being included in the study.
: Not applicable.