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临床试验/JPRN-UMIN000030128
JPRN-UMIN000030128已完成未知

The Japanese Study for Efficacy of Luseogliflozin on composite Endpoint, Compared to DPP-4 inhibitors, in Type 2 diabetes mellitus patients (J-SELECT study) - The Japanese Study for Efficacy of Luseogliflozin on composite Endpoint, Compared to DPP-4 inhibitors, in Type 2 diabetes mellitus patients (J-SELECT study)

Japan Physicians Association0 个研究点目标入组 623 人开始时间: 2017年11月27日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
623

研究概览

简要总结

npublished because the results of this study is now submitted to an academic journal

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • Patients who fall into any of the following criteria are excluded from participating in the study. 1. Type 1 diabetes mellitus or secondary diabetes 2. Patients who used insulin, GLP-1 analogs, or SU within 8 weeks before consenting 3. Patients who had myocardial infarction, cerebral infarction, or stroke within 12 weeks before giving their consent 4. Patients with severe liver disease (Patients with AST or ALT value five times or more of the upper limit of the stand value in each research institution) 5. Patients with serious renal disease (eGFR less than 30 mL/min/1.73m2) 6. Patients with unstable hypertension and dyslipidemia 7. Dehydrated patients (patients complain to have a symptom of dehydration) 8. Patients with urinary tract infection or genital infection 9. Patients who are breastfeeding, pregnant, possibly pregnant, or planning to be pregnant 10. Contraindication: patients with hypersensitivity to any medical component of each study drug 11. Patients who need legal representative for giving consent 12.Patients with other conditions that the investigator/researcher thinks inappropriate for the study

研究者

发起方
Japan Physicians Association

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