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临床试验/NCT03642184
NCT03642184终止4 期

Efficacy and Safety of Empagliflozin Compared With Linagliptin in New-onset Diabetes Mellitus After Kidney Transplantation

RenJi Hospital1 个研究点 分布在 1 个国家目标入组 6 人开始时间: 2018年7月14日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
终止
入组人数
6
试验地点
1
主要终点
eGFR

研究概览

简要总结

This is an open label, randomized controlled study. We'd like to access the safety and effects of empagliflozin compared with linagliptin in new-onset diabetes after kidney transplantation patients. Our primary endpoints are kidney related indicators and secondary endpoints are glucose and lipid metabolism related indicators and adverse events. We are going to recruit 35 patients for each group and follow six months.

详细描述

In recent years, with the development of transplantation technology and immunosuppressive agents, kidney transplantation has made considerable progress. However, for metabolic disorders after kidney transplantation, such as new diabetes after kidney transplantation, there is still insufficient awareness. Since 1964, Starlz et al. first discovered and proposed New-onset diabetes after kidney transplantation(NODAT) in patients after renal transplantation. Scholars from all countries have paid considerable attention to it. The Chinese guidelines indicate that NODAT can increase the risk of graft-related complications, such as rejection, graft loss and infection, and ultimately affect the long-term survival of the recipient. In addition, NODAT has also been shown to increase the risk of cardiovascular events, and cardiovascular disease is associated with more than half of kidney transplant deaths. A retrospective study of 567 renal transplant recipients in China showed that the incidence of NODAT was 24.2%. It can be seen that the incidence of new-onset diabetes after renal transplantation is high and has long-term adverse effects on transplant patients. Therefore, there is an urgent need to evaluate and investigate NODAT's therapeutic drug regimens.

According to the study, empagliflozin has a protective effect on the kidney and cardiovascular system, but it has not yet been written into the treatment guidelines for new-onset diabetes after kidney transplantation. Metformin and linagliptin are frequently used in diabetics after renal transplantation, and linagliptin also have a protective effect on the kidneys. Therefore, this experiment wanted to compare the effects between empagliflozin and linagliptin on kidney protection.

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
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Single kidney transplantation
  • Normal glucose tolerance or Pre-Diabetes mellitus before transplantation
  • According to Oral glucose tolerance test results to make the diagnosis of NODAT
  • Standard triple immunosuppression therapy
  • HbA1c≤10%
  • Steady hormone usage
  • BMI 18.5-30kg/m2
  • Patient informed consent

排除标准

  • Diabetes patients before transplantation
  • Pregnancy pregnancy
  • Type 1 diabetes after kidney transplantation
  • Severe liver function impairment (AST/ALT 3 times standard value)
  • Severely impaired renal function (eGFR<45)
  • Having uncontrolled diseases
  • History of cancer in the past 5 years (except basal cell carcinoma) and/or cancer treatment
  • Participating in another trial involving the study drug with in 30 days
  • Premenopausal women (1 year before the last menstrual period ≤ informed consent)
  • Alcohol or drug abuse within 3 months of informed consent, affecting compliance Need other drugs to control NODAT

研究组 & 干预措施

Empagliflozin

Active Comparator

Jardiance 10mg/25mg Film-coated tablets, once daily

干预措施: Empagliflozin (Drug)

Linagliptin

Active Comparator

Trajenta 5mg Film-coated tablets, once daily

干预措施: Linagliptin (Drug)

结局指标

主要结局

eGFR

时间窗: 24 weeks

the change from baseline in estimated glomerular filtration rate calculated by MDRD formula

次要结局

  • Acute rejection(24 weeks)
  • Progression to albuminuria(24 weeks)
  • Adverse events(24 weeks)
  • Graft loss rate(24 weeks)
  • Progression to macroalbuminuria(24 weeks)
  • Fasting plasma glucose(24 weeks)
  • Glycated hemoglobin (HbA1c)(24 weeks)
  • Mortality rate(24 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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