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
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