IRCT201008304582N2已完成3 期
Comparison of efficacy and safety of Tramadol, Paroxetine and placebo in patients with life long premature ejaculation
rology Research Centre0 个研究点目标入组 150 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 150
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
- 年龄范围
- 18 years 至 50 years（—）
- 性别
- Male
入选标准
- •at least one year of their marriage is past; to be between 18-50 years of age; have the possibility of intercourse at least once a week, ability to read and write
- •Exclusion criteria: People who have a history of mental diseases, a physical illness such as diabetes and liver disease, alcohol or drug abuse, a history of surgery that has been effective on sexual function; history of endocrine disease, prostatitis; history of paroxetine and tramadol during the last 3 months
排除标准
- 未提供
研究者
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