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临床试验/ACTRN12612000235808
ACTRN12612000235808进行中(未招募)不适用

Assessing predicting factors of satisfaction for patients with refractory erectile dysfunction and their female partners from penile prosthesis implantation

Aristotle University of Thessaloniki0 个研究点目标入组 50 人开始时间: 2012年2月24日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Non-randomised trial
主要目的
Treatment

入排标准

年龄范围
o limit 至 o limit(—)
性别
Male

入选标准

  • 1.Patients with refractory to oral and intracavernosal injection treatment erectile dysfunction not allowing sexual intercourse .
  • 2.Contraindication for oral and intracavernosal injection treatment for patients with erectile dysfunction not allowing sexual intercourse.
  • 3.Unwilling for oral and intracavernosal injection treatment patients with erectile dysfunction not allowing sexual intercourse.
  • 4. Patients with refractory to oral treatment erectile dysfunction not allowing sexual intercourse, who do not wish to receive intracavernosal injections

排除标准

  • 1.Patients with erectile dysfunction safely curable by oral or intracavernosal injection treatment
  • 2.Patients, who despite their refractory erectile dysfunction in oral and intracavernosal injection treatment, can have sexual intercourse

研究者

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