跳至主要内容
临床试验/JPRN-jRCTs071180091
JPRN-jRCTs071180091招募中未知

A clinical study for cardioprotective effect of empagliflozin in T2DM patients with heart failure and exploring associated factors - EMPOWERMENT

Ide Tomomi0 个研究点目标入组 40 人开始时间: 2019年3月29日最近更新:

试验速览

阶段
未知
状态
招募中
发起方
入组人数
40

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
>= 20age old 至 <= 85age old(—)
性别
All

入选标准

  • 1)Age >20 years and <85 years males and females
  • 2)Inadequately controlled type 2 diabetic patients HbA1c >= 6.0% and HbA1c < 10%
  • 3)Type 2 diabetic patients with LV ejection fraction > 50% and a symptom of heart failure (NYHA II or III)
  • 4)BNP >= 35pg/dL
  • 5)Patients from whom a written informed consent are obtained

排除标准

  • 1)Other than T2DM such as T1DM and secondary DM.
  • 2)Patients with severe infection, perioperative patients, patients with severe trauma.
  • 3)Patientsreceiving SGLT2 inhibitor and/or incretin-related drugs within 2 months before ingestion of study drug.
  • 4)Patients with idiopathic cardiomyopathy, Fabry disease, Amyloidosis cardiomyopathy.
  • 5)Patientswithrenal insufficiency (eGFR< 45 ml/min/1.73m2).
  • 6)Patients with severe respiratory disease, severe musculoskeletal conditions and unable to exercise challenge test for any other diseases, and severe anemia.
  • 7)Any uncontrolled endocrine disorder except type 2 diabetes.
  • 8)Acute coronary syndrome, stroke, or transient ischemic attack within 3 months of IC.
  • 9)Patient who is scheduled to undergo surgery within 3 months before IC or plan to operate within 3 months after IC.
  • 10)Patients who have a heart pacemaker, who have an aneurysm clip in their brain more than 20 years ago, or have a body implantationdevice(Implantedcardioverter-defibrillator ,Cochlear,otologic,or other ear implant, or Neurostimulation system).
  • 11)Patients with severe claustrophobia.
  • 12)Patients who are pregnant or breast-feeding.
  • 13)Patients lower than BMI 20.
  • 14)Patients in hyperglycemic crisis or accompanied with marked symptom of hyperglycemia and /or DKA.
  • 15)Patients considered inappropriate to participate in the study by the principal and/or sub- investigators.

研究者

发起方
Ide Tomomi

相似试验