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临床试验/JPRN-jRCTs071180041
JPRN-jRCTs071180041已完成4 期

Prevention of atherosclerosis by SGLT2inhibitor: a multicenter, randomized controlled study - PROTECT

ode Koichi0 个研究点目标入组 482 人开始时间: 2019年3月14日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
482

研究概览

简要总结

A total of 482 subjects were equally randomized to the ipragliflozin and control groups. Changes of the mean CCA-IMT for 24 months, which was the primary endpoint, was 0.0013 mm in the ipragliflozin group, and 0.0015 mm in the control group, and the estimated between-group difference(ipragliflozin group-control group) was -0.0001mm (P=0.989). These results suggest that 24-month treatment of ipragliflozin, compared to conventional therapy, in patients with type 2 diabetes had no impact on the CCA-IMT.

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 20age old 至 ot applicable(—)
性别
All

入选标准

  • 1) Type 2 diabetes with HbA1c (NGSP) >=6.0% and less than10.0% despite diet/exercise therapy or diet/exercise therapy adding antidiabetic agents for over three months
  • 2)over 20 years of age at the time of informed consent acquisition and hospitalization or outpatient
  • 3) The patient provided with information about the study,submitted written informed consent to it

排除标准

  • 1) Type 1 diabetes
  • 2) Has history of severe ketosis, diabetic coma, or precoma within 6 months
  • 3) Has severe infection, serious trauma, or pre or post surgery (including carotid endarterectomy and stent implantation)
  • 4) With severe renal dysfunction (eGRF <45 mL/min/1.73m2 or patient undergoing artificial dialysis)
  • 5) Has history of myocardial infarction, angina, percutaneous transluminal coronary angioplasty, coronary artery bypass graft, cerebral infarction, intracranial hemorrhage, subarachnoid hemorrhage and transient ischemic attacks within 3 months before initiation of the study
  • 6) Heart failure patient whose NYHA functional classification is III or IV
  • 7) Has history of administration of SGLT-2 within 1 month before initiation of the study
  • 8) Pregnant, possibly pregnant, planned to become pregnant or nursing women
  • 9) Has history of hypersensitivity to ipragliflozin or any other excipient of ipragliflozin
  • 10) Are considered not eligible for the study by the attending doctor due to other reasons

研究者

发起方
ode Koichi

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