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临床试验/JPRN-UMIN000023035
JPRN-UMIN000023035已完成未知

Evaluation of the efficacy and safety of luseogliflozin and changes in QOL - Evaluation of the efficacy and safety of luseogliflozin and changes in QOL (Lusefi QOL study)

The Institute for Adult Diseases, Asahi Life Foundation0 个研究点目标入组 64 人开始时间: 2016年7月11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
64

研究概览

简要总结

暂无简介。

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

  • 1) Patients with diabetes other than type 2 diabetes 2) Patients with a history of cardiovascular events such as cerebral infarction and myocardial infarction. 3) Patients with serious renal or hepatic dysfunction 4) Patients with malignant tumors (those who have a history of malignant tumors but are currently receiving no treatment and had no recurrence, and those considered unlikely to have any recurrence during the study period are eligible for the study). 5) Patients with repeated genital or urinary tract infections 6) Patients with eGFR <=30 mL/min/1.73 m2 7) Patients with BMI <=20 8) Patients for whom dosage and administration of concomitant antidiabetic drugs have been changed within the 12 weeks prior to the start of administration of the study drug. 9) Patients who have administered a SGLT2 inhibitor within 6 months prior to the start of administration of the study drug 10) Patients whose answers to the questionnaire at week 0 were not collected before the start of administration. 11) Patients deemed unsuitable for participation in the study by the investigator or sub-investigator due to other reasons.

研究者

发起方
The Institute for Adult Diseases, Asahi Life Foundation

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