跳至主要内容
临床试验/EUCTR2004-004086-15-DE
EUCTR2004-004086-15-DE进行中(未招募)1 期

Comparison of nephrotoxic effects of the contrast dyes iodixanol (iso-osmolar, non-ionic, dimer) and ioversol (low-osmolar, non-ionic, monomer) in patients with impaired renal function and severe heart failure

niversity Hospital of Frankfurt, Department of Cardiology0 个研究点目标入组 140 人开始时间: 2005年5月17日最近更新:

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
140

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • - Patients must be older than 18 y.o.
  • - Written consent to the study
  • - Coronary angiography is required for medical reasons
  • - Calculated glomerular filtration rate = 60 ml/min (calculation is based on the shortened MDRD-formula)
  • - Severe heart failure, diagnosed either by an ejection fraction = 45 % (echocardiography) or a clinical condition NYHA III or IV
  • 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
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - Severe comorbidity (i.e. neoplasia, life expectaning = 2 yrs.)
  • - Intravacular administration of iodinated contrast dye within last 14 days
  • - Intake of nephrotoxic drugs within the last 7 days
  • - Intake of metformine within the last 24 hours
  • - Patients with prior renal transplantation
  • - End-stage renal disease or acute renal failure and/or necessity of dialysis after coronary angiography
  • - Pregnancy or lactation
  • - Impaired liver function following the Child-Pugh criteria according a severity level of Child B or C

研究者

发起方
niversity Hospital of Frankfurt, Department of Cardiology

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