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临床试验/NL-OMON36940
NL-OMON36940已完成4 期

Comparative study of pharmacokinetics of amlodipine besilate oral liquid and tablets in healthy Dutch volunteers - Pharmacokinetics of amlodipine besilate oral liquid and tablets

Erasmus MC, Universitair Medisch Centrum Rotterdam0 个研究点目标入组 12 人开始时间: 待定最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
12

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
18 至 99(—)

入选标准

  • Subject is healthy
  • Subject is Caucasian
  • Age is between 18-55 years
  • Body Mass Index (BMI) is between 19-25
  • Written informed consent

排除标准

  • Sitting blood pressure lower than 120 mmHg systolic and/or 80 mmHg diastolic in resting conditions
  • Use of medication, both medicines on prescription and over-the-counter medicines, excluding contraceptives
  • Subject is familiar with one of the contra-indications of amlodipine: hypersensitivity to dihydropyridine derivatives, severe hypotension, shock (including cardiogenic shock), obstruction of the outflow tract of the left ventricle (e.g. aortic stenosis), hemodynamically unstable heart failure after acute myocardial infarction
  • Allergy for one of the substances of both formulations
  • Subject has history of alcohol or drug abuse

研究者

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