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
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