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临床试验/EUCTR2013-002437-37-NL
EUCTR2013-002437-37-NL进行中(未招募)1 期

Effects on Intra-Coronary Attenuation using low iodine concentrations (240 mg, 300 mg and 370 mg iodine per ml) while maintaining identical IDR - EICAR

Maastricht University Medical Centre0 个研究点目标入组 390 人开始时间: 2014年3月18日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
390

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

  • no previous cardiovascular history
  • atypical or typical complaints of angina
  • patient aged older than 18 and competent
  • 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 195
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 195

排除标准

  • contraindications for cCTA
  • (inability to perform a breath hold for at least expected scan time, unstable angina, hemodynamic instability, history of CAD, pregnancy, renal insufficiency defined as GFR <45 ml/min, iodine allergy)
  • unable to give informed consent or no informed consent obtained
  • inability to position an 18G cannula in an antecubital vein

研究者

发起方
Maastricht University Medical Centre

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