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临床试验/CTRI/2010/091/001506
CTRI/2010/091/001506已完成2 期

A double blind, randomized, placebo controlled study to evaluate the effect of ProSolutionTM pills in enhancing sexual function of men with erectile dysfunction

eading Edge Marketing, PO Box CR-56766, Suite 1210Nassau Bahamas0 个研究点目标入组 84 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
84

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

入选标准

  • Males aged 25-50 years, involved in a stable heterosexual relationship of >6 months
  • Subjects with Erectile Dysfunction (ED) since at least 3 months
  • IIEF-A (Erectile Function) score in the range of 11 ? 23
  • IIEF-B score (Other than Erectile Function) in the range of 21 - 35

排除标准

  • Significant cardiovascular or any other co-morbidities
  • Use of sildenafil or any other phosphodiesterase type inhibitor within previous 6 weeks
  • Current use of any other therapy for treatment of ED
  • Subjects with Diabetes
  • Subjects with Hypertension
  • Subjects taking medications known to cause ED
  • Subjects with major psychiatric disorders
  • Subjects with Low Testosterone Levels (<200 ng/dl)
  • Subjects with history of spinal cord injury or a radical prostatectomy or radical pelvic surgery.
  • Subjects with anatomical deformity of the penis which has a severe effect on sexual functioning
  • Subjects with HIV or AIDS or any other sexually transmitted disease
  • Subjects with Hyperprolactinemia

研究者

发起方
eading Edge Marketing, PO Box CR-56766, Suite 1210Nassau Bahamas

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