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临床试验/NCT02890745
NCT02890745已完成2 期

EMPOX - A Randomised, Double-blinded, Placebo Controlled Study That Evaluates the Effect of Empagliflozin on Oxidative Stress in Patients With Type 2 Diabetes

Henrik Enghusen Poulsen1 个研究点 分布在 1 个国家目标入组 31 人开始时间: 2016年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
31
试验地点
1
主要终点
Urinary excretion of 8-oxo-7,8-dihydroguanosine (nmol/24h)

研究概览

简要总结

The purpose of this study is to investigate the effect of empagliflozin on oxidative stress in patients with type 2 diabetes. The association is examined by comparing the difference in oxidative modifications before and after 14 days treatment with 25 mg empagliflozin compared to placebo treatment. The study is randomised, double-blinded, and placebo controlled. Each treatment group consists of 17 males with type 2 diabetes. Oxidative modifications are measured by urinary excretion of 8-oxo-7,8-dihydro-2'-deoxyguanosine and 8-oxo-7,8-dihydroguanosine. A student t-test will be performed to compare the drug treatment with placebo. The results will be published in a peer-review journal.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Diagnosed with type 2 diabetes
  • HbA1c: 6.5-9.0%
  • Capable of understanding oral- and written information
  • Caucasian

排除标准

  • Estimated glomerular filtration rate (eGFR) < 60 mL/hour/1.73 m2
  • Currently receiving insulin treatment
  • Coronary artery bypass grafting, percutaneous coronary intervention, acute coronary syndrome, stroke, lung embolism, deep vein thrombosis, or transitory cerebral ischemia within 6 months
  • Genital infection within 14 days
  • Plasma alanine aminotransferase ≥3 times upper normal limit
  • Treatment with sodium glucose cotransporter (SGLT) -2 inhibitor within 2 months
  • Hyperglycaemic symptoms
  • Psychiatric disorder
  • Intolerance to empagliflozin or other agents relevant to study
  • Non-compliant

研究组 & 干预措施

Empagliflozin

Experimental

One tablet 25 mg empagliflozin every morning for 14 days

干预措施: Empagliflozin (Drug)

Placebo

Placebo Comparator

One tablet placebo every morning for 14 days

干预措施: Placebo (Drug)

结局指标

主要结局

Urinary excretion of 8-oxo-7,8-dihydroguanosine (nmol/24h)

时间窗: Change from baseline after fourteen days of intervention

Urinary excretion of 8-oxo-7,8-dihydro-2'-deoxyguanosine (nmol/24h)

时间窗: Change from baseline after fourteen days of intervention

次要结局

  • Plasma levels of malondialdehyde(Change from baseline after fourteen days of intervention)
  • Plasma levels of iron, ferritin, transferrin and transferrin saturation(Measured at baseline and after intervention)

研究者

发起方
Henrik Enghusen Poulsen
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Henrik Enghusen Poulsen

Professor, DMSc, chief physician

Rigshospitalet, Denmark

研究点 (1)

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