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临床试验/NCT02528019
NCT02528019Unknown4 期

Effects of the DPP-4 or SGLT2 Inhibitors on the Metabolic Cardiovascular Systems in Patients With Type 2 Diabetes Mellitus.

Kurume University1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2015年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
入组人数
100
试验地点
1
主要终点
Effects of treatment on the nominal change in arterial stiffness from baseline after 6 months of treatment as measured by cardio-ankle vascular index

研究概览

简要总结

Inhibition of dipeptidyl peptidase-4 (DPP-4) or sodium-glucose co-transporter type 2 (SGLT2) has been proposed as a therapeutic target for type 2 diabetes. However, how DPP-4 inhibitors or SGLT2 inhibitors exert protective actions for diabetic complications in addition to their glucose-lowering effects remains unknown.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
30 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Clinical diagnosis of type 2 diabetic patients
  • Must be able to swallow tablets
  • never received DPP-4 inhibitors or SGLT2 inhibitors

排除标准

  • uncontrolled diabetes (fasting plasma glucose>200 mg/dL)
  • receiving insulin therapy
  • hepatic disorders (2.5 fold or greater increases in aspartate transaminase or alanine transaminase levels above the upper limits of normal)
  • inflammatory disorders
  • neoplastic disorders
  • recent (<3months) acute coronary syndrome and stroke
  • any acute infection

研究组 & 干预措施

DPP-4 inhibitors

Active Comparator

sitagliptin (25-100mg daily), vildagliptin (50-100mg daily), alogliptin (12.5-25mg daily), linagliptin (2.5-5mg daily), teneligliptin (20-40mg), anagliptin (100-200mg daily), saxagliptin (2.5-5mg daily) or trelagliptin (50-100mg weekly)

干预措施: DPP-4 inhibiotors (Drug)

SGLT2 inhibitors

Active Comparator

ipragliflozin (50-100mg daily), dapagliflozin (5-10mg daily), luseogliflozin (2.5-5mg), tofogliflozin (20mg daily), canagliflozin (100mg daily) or empagliflozin (10-25mg daily)

干预措施: SGLT2 inhibitors (Drug)

Glimepiride

Active Comparator

glimepiride (0.5-8mg daily)

干预措施: Glimepiride (Drug)

结局指标

主要结局

Effects of treatment on the nominal change in arterial stiffness from baseline after 6 months of treatment as measured by cardio-ankle vascular index

时间窗: 6 months of treatment

次要结局

  • Change from baseline in subcutaneous and visceral fat volume(6 months of treatment)
  • Change from baseline in lipid profile including malondialdehyde-modified low-density lipoprotein and remnant-like particle cholesterol(6 months of treatment)
  • Change from baseline in circulating inflammatory markers(6 months of treatment)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Nobuhiro Tahara

Associate Professor

Kurume University

研究点 (1)

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