CTRI/2017/09/009618已完成2 期
An open label, interventional, multi-center, prospective clinical study to Evaluation of Efficacy and Safety of JP-16 Capsules in Patients Suffering from Mild to Moderate Sexual Dysfunction - NI
Chatarubhuj Pharmaceutical Co0 个研究点目标入组 40 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
- 40
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
- •1. Subjects who have scored 22 to 25 on the Erectile Function (EF) domain of the International Index of Erectile Function (IIEF) at screening.
- •2. Subject without any organic cause of Sexual Dysfunction.
- •3. Subjects should be in an active stable sexual relationship for the duration of study
排除标准
- •1. Subjects with major illnesses and sexual dysfunction due to anatomical, surgical or pharmacological causes
- •2. Subjects with total erectile failure or any other sexual disorder
- •3. Subjects with history of disorders that may cause priapism
- •4. Subjects with history of major psychiatric disorder
- •5. Subjects with history of central nervous system disorders such as stroke, transient ischemic attacks or spinal cord injury or pelvic surgery
- •6. Patients with preexisting systemic disease necessitating long-term medications, genetic and endocrinal disorders
研究者
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进行中（未招募）
不适用
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