KCT0001827已完成未知
A Multi-center, Open, Single-arm design Clinical study to Evaluate the Efficacy and Safety of PowerFill for Penile Enhancement
REGEN Biotech0 个研究点目标入组 23 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 23
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional Study
入排标准
- 年龄范围
- 20(Year) 至 65(Year)（—）
- 性别
- Male
入选标准
- •(1) healthy men, aged 20 to 65
- •(2) men with small penis syndrome
- •(3) during the study period, subject will not received any treatments associated with penile augmentation
- •(4) after 1month, subject can perform the sexual intercourse
- •(5) subject will agree with investigator's decision
- •(6) subject will sign an informed consent form
排除标准
- •(1) any history of psychological or psychiatric illness,
- •(2) congenital or acquired penile malformation including severe phimosis,
- •(3) previous PA history,
- •(4) any chronic major systemic disease including diabetes and coagulopathy
研究者
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