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临床试验/ISRCTN66772971
ISRCTN66772971已完成未知

Erectile dysfunction: a randomised controlled trial of lipid lowering with simvastatin (EDS trial)

niversity of Hertfordshire (UK)0 个研究点目标入组 170 人开始时间: 2008年9月26日最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
170

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
Male

入选标准

  • 1. Men aged 40 years and over
  • 2. In a stable heterosexual relationship for at least 6 months
  • 3. No clinically overt cardiovascular risk factors other than raised cholesterol
  • 4. Not currently on lipid or erectile dysfunction therapy
  • 5. Untreated erectile dysfunction defined as score <22 on the International Index of Erectile Function 5 item questionnaire

排除标准

  • 1. Diabetes, past history of myocardial infarction, hospitalised angina or stroke
  • 2. Hypertension - systolic blood pressure >=170 mmHg, diastolic >=100 mmHg
  • 3. Ratio total:high-density lipoproteins (HDL) cholesterol >=6
  • 4. Total cardiovascular risk >= 20% over next 10 years
  • 5. Current lipid lowering therapy
  • 6. Erectile dysfunction therapy in the last 3 months
  • 7. Hypogonadism
  • 8. Chronic liver disease or abnormal liver function
  • 9. Severe renal disease or evidence of impaired renal function
  • 10. Inflammatory muscle disease or evidence of muscle problems
  • 11. Concomitant administration of contra-indicated drugs: itraconazole, ketoconazole, HIV protease inhibitors, erythromycin, telithromycin and nefazodone
  • 12. Concomitant administration of other drugs associated with increased risk of myopathy/rhabdomyolysis: ciclosporin, danazol and fusidic acid
  • 13. Galactose intolerance, Lapp lactase deficiency or glocose-galactose malabsorption

研究者

发起方
niversity of Hertfordshire (UK)

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