<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(2)</volume><submitter>Tanaka A</submitter><funding>Astellas Pharma US</funding><pubmed_abstract>&lt;h4>Aims&lt;/h4>To examine the effects of a 24-month treatment with ipragliflozin on carotid intima-media thickness (IMT) in type 2 diabetes patients.&lt;h4>Methods and results&lt;/h4>In this multicenter, prospective, randomized, open-label, and blinded-endpoint investigator-initiated clinical trial, adults with type 2 diabetes and haemoglobin A1C (HbA1c) of 6.0-10.0% (42-86 mmol/mol) were randomized equally to ipragliflozin (50 mg daily) and non-sodium-glucose cotransporter-2 (SGLT2) inhibitor use of standard-care (control group) for type 2 diabetes and were followed-up to 24 months. The primary endpoint was the change in mean common carotid artery IMT (CCA-IMT) from baseline to 24 months. A total of 482 patients were equally allocated to the ipragliflozin (N = 241) and control (N = 241) groups, a</pubmed_abstract><journal>European heart journal. Cardiovascular pharmacotherapy</journal><pagination>165-172</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9892869</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Effect of ipragliflozin on carotid intima-media thickness in patients with type 2 diabetes: a multicenter, randomized, controlled trial.</pubmed_title><pmcid>PMC9892869</pmcid><pubmed_authors>Kajikawa M</pubmed_authors><pubmed_authors>Hisauchi I</pubmed_authors><pubmed_authors>Yoshiyama M</pubmed_authors><pubmed_authors>Kanbara T</pubmed_authors><pubmed_authors>Miura SI</pubmed_authors><pubmed_authors>Nasuno T</pubmed_authors><pubmed_authors>Ogata Y</pubmed_authors><pubmed_authors>Takahara K</pubmed_authors><pubmed_authors>Ohguchi S</pubmed_authors><pubmed_authors>Kitakaze M</pubmed_authors><pubmed_authors>Murohara T</pubmed_authors><pubmed_authors>Sugimoto K</pubmed_authors><pubmed_authors>Otsuka T</pubmed_authors><pubmed_authors>Fukae S</pubmed_authors><pubmed_authors>Teragawa H</pubmed_authors><pubmed_authors>Inoue T</pubmed_authors><pubmed_authors>Eguchi K</pubmed_authors><pubmed_authors>Kuroda A</pubmed_authors><pubmed_authors>Kurano M</pubmed_authors><pubmed_authors>Yamashina A</pubmed_authors><pubmed_authors>Kanda J</pubmed_authors><pubmed_authors>Yamada H</pubmed_authors><pubmed_authors>Maruhashi T</pubmed_authors><pubmed_authors>Takamori A</pubmed_authors><pubmed_authors>Shiga Y</pubmed_authors><pubmed_authors>Koikawa K</pubmed_authors><pubmed_authors>PROTECT study investigators</pubmed_authors><pubmed_authors>Machii N</pubmed_authors><pubmed_authors>Furuta M</pubmed_authors><pubmed_authors>Arimura T</pubmed_authors><pubmed_authors>Doi M</pubmed_authors><pubmed_authors>Ishihara M</pubmed_authors><pubmed_authors>Kishi H</pubmed_authors><pubmed_authors>Koyosue A</pubmed_authors><pubmed_authors>Ikehara Y</pubmed_authors><pubmed_authors>Narisawa M</pubmed_authors><pubmed_authors>Asano H</pubmed_authors><pubmed_authors>Shuto T</pubmed_authors><pubmed_authors>Ajioka M</pubmed_authors><pubmed_authors>Higashi Y</pubmed_authors><pubmed_authors>Takase B</pubmed_authors><pubmed_authors>Kitagawa K</pubmed_authors><pubmed_authors>Koga S</pubmed_authors><pubmed_authors>Uchimura Y</pubmed_authors><pubmed_authors>Hironori K</pubmed_authors><pubmed_authors>Shibata Y</pubmed_authors><pubmed_authors>Tanaka K</pubmed_authors><pubmed_authors>Uehara H</pubmed_authors><pubmed_authors>Sakuma M</pubmed_authors><pubmed_authors>Sohmiya K</pubmed_authors><pubmed_authors>Mirii J</pubmed_authors><pubmed_authors>Wakami K</pubmed_authors><pubmed_authors>Fukumoto K</pubmed_authors><pubmed_authors>Yoshida R</pubmed_authors><pubmed_authors>Ohte N</pubmed_authors><pubmed_authors>Nanasato M</pubmed_authors><pubmed_authors>Yoshida H</pubmed_authors><pubmed_authors>Bando Y</pubmed_authors><pubmed_authors>Nakano J</pubmed_authors><pubmed_authors>Kaneko T</pubmed_authors><pubmed_authors>Kanzaki 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T</pubmed_authors><pubmed_authors>Sata M</pubmed_authors><pubmed_authors>Asaka M</pubmed_authors><pubmed_authors>Ueda S</pubmed_authors><pubmed_authors>Matsuhisa M</pubmed_authors><pubmed_authors>Tomiyama H</pubmed_authors><pubmed_authors>Gima Y</pubmed_authors><pubmed_authors>Kudo A</pubmed_authors><pubmed_authors>Okada Y</pubmed_authors><pubmed_authors>Ise T</pubmed_authors><pubmed_authors>Kamiya H</pubmed_authors><pubmed_authors>Hatano S</pubmed_authors><pubmed_authors>Sonoda S</pubmed_authors><pubmed_authors>Shimizu W</pubmed_authors><pubmed_authors>Kario K</pubmed_authors><pubmed_authors>Akasaki Y</pubmed_authors><pubmed_authors>Miyazaki M</pubmed_authors><pubmed_authors>Nago C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Effect of ipragliflozin on carotid intima-media thickness in patients with type 2 diabetes: a multicenter, randomized, controlled trial.</name><description>&lt;h4>Aims&lt;/h4>To examine the effects of a 24-month treatment with ipragliflozin on carotid intima-media thickness (IMT) in type 2 diabetes patients.&lt;h4>Methods and results&lt;/h4>In this multicenter, prospective, randomized, open-label, and blinded-endpoint investigator-initiated clinical trial, adults with type 2 diabetes and haemoglobin A1C (HbA1c) of 6.0-10.0% (42-86 mmol/mol) were randomized equally to ipragliflozin (50 mg daily) and non-sodium-glucose cotransporter-2 (SGLT2) inhibitor use of standard-care (control group) for type 2 diabetes and were followed-up to 24 months. The primary endpoint was the change in mean common carotid artery IMT (CCA-IMT) from baseline to 24 months. A total of 482 patients were equally allocated to the ipragliflozin (N = 241) and control (N = 241) groups, a</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2026-07-16T20:12:02.163Z</modification><creation>2025-04-05T23:21:23.018Z</creation></dates><accession>S-EPMC9892869</accession><cross_references><pubmed>36308299</pubmed><doi>10.1093/ehjcvp/pvac059</doi></cross_references></HashMap>