跳至主要内容
临床试验/EUCTR2006-006706-29-NL
EUCTR2006-006706-29-NL进行中(未招募)1 期

Does atorvastatin reduce ischemia-reperfusion injury in humans in-vivo? - ator

MCN department Pharm-Tox0 个研究点目标入组 20 人开始时间: 2006年12月22日最近更新:
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
20

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
Male

入选标准

  • -Age 18-50 years
  • -Informed consent
  • -Physical able to perform ischemic exercise
  • 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) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - History of any cardiovascular disease
  • - Hypertension (in supine position: systole > 140 mmHg, diastole > 90 mmHg)
  • - Diabetes mellitus (fasting glucose > 7.0 mmol/L or random glucose > 11.0 mmol/L)
  • - Hyperlipidaemia (fasting total cholesterol > 5.5 mmol/l)
  • - Alanine-Amino-Transferase (ALAT) >90 U/L (more than twice the upper level of the normal range)
  • - Creatinine Kinase (CK) >340 U/L (more than twice the upper level of the normal range)
  • - Drug abuse
  • - Concomitant chronic use of medication
  • - Administration of radioactivity in research setting during the last 5 years
  • - Participation to any drug-investigation during the previous 60 days as checked with VIP check according to CRCN standard procedures

研究者

发起方
MCN department Pharm-Tox

相似试验