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临床试验/EUCTR2020-005713-40-FR
EUCTR2020-005713-40-FR招募中1 期

Acute Reno-Cardiac Action of Dapagliflozin In Advanced Heart Failure patients on heart transplant waiting list: a multicenter, double-blind, randomized clinical trial. - ARCADIA-HF

Hospices Civils de Lyon0 个研究点目标入组 80 人开始时间: 2021年5月27日最近更新:
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试验速览

阶段
1 期
状态
招募中
入组人数
80

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

性别
All

入选标准

  • 1)Patient has signed informed consent form
  • 2)Age = 18 years
  • 3)NYHA class =3
  • 4)LVEF = 35%
  • 5)On optimal medical management (OMM) based on current heart failure practice guidelines at maximal tolerated dose for at least 30 days
  • 6)On waiting list for heart transplantation after multidisciplinary Heart Team decision, with anticipated access to heart transplant = 6 months
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 70
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 10

排除标准

  • 1)Priority patient on waiting list for heart transplantation
  • 2)Etiology of heart failure due to or associated with uncorrected thyroid disease, obstructive cardiomyopathy, pericardial disease, amyloidosis or restrictive cardiomyopathy
  • 3)Inotrope dependent, existence of ongoing mechanical circulatory support
  • 4)Current acute decompensated HF or hospitalization due to decompensated HF <30 days prior to the enrolment
  • 5)History of any organ transplant or prior implantation of a ventricular assistance device (VAD) or similar device, or implantation expected after randomization
  • 6)Presence of an active, uncontrolled infection
  • 7)Any recent interventional procedure likely to improve symptoms and heart failure status (coronary revascularization, percutaneous mitral valve intervention, cardiac resynchronization therapy) < 60 days
  • 8)Glomerular filtration rate < 30 ml/min/1.73 m2, according to CKD-EPI formula
  • 9)Unstable or rapidly progressing renal disease
  • 10)Patients with severe hepatic impairment (Child-Pugh class C)
  • 11)Chronic treatment with dapagliflozin or other SGLT2 inhibitors
  • 12)Patient with known history of severe drug intolerance to dapagliflozin or any excipients of the dapagliflozin (galactose, lactase)
  • 13)Type 1 diabetes mellitus
  • 14)Any surgical or medical condition which might significantly alter the absorption, distribution, metabolism, or extraction of study drug at investigators’ discretion
  • 15)Participation in another clinical interventional trial
  • 16)Any condition other than heart failure that could limit survival to less than 24 months
  • 17)Positive pregnancy test if of childbearing potential or refusal to use adequate contraception or women breast-feeding
  • 18)Patients with any legal protection measure
  • 19)Patients without any health coverage
  • 20)Psychiatric disease/disorder, irreversible cognitive dysfunction or psychological issues that are likely to impair compliance

研究者

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