ITMCTR2200005688招募中未知
a Random, Double-blind, Double-simulation, Multicenter study of Chinese Herbal Compound Jinji Granules (CJG) for treatment Primary Premature Ejaculation: (Gan depression an Shen deficiency syndrome)
适应症
试验速览
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
- 23 至 50(—)
- 性别
- Male
入选标准
- •(1)Meet the diagnostic criteria of Western medicine for premature ejaculation;
- •(2)Meet the standard of TCM syndrome differentiation.
- •(3)The course of disease is more than 1 year.
- •(4)23=age=50.
- •(5)Sexual frequency=1 time/week, at least 6 times a month.
- •(6)At least in the last 3 months and during the course of this study, the subject had stable marital relationship or stable adult female sexual partner.
- •(7)Normal erectile function, IIEF-5 score > 21 [20-23].
- •(8)Subjects agree not to use any other drugs for premature ejaculation during the study period, including 5-HT inhibitors, Chinese herbal medicines (including decoction and proprietary Chinese medicine), or devices used for PE treatment.
- •(9)Subjects (including partners) guarantee that they have no birth plan and voluntarily use appropriate contraceptive measures during the study period up to 3 months after the last medication.
- •(10)The subject voluntarily signs the informed consent.
排除标准
- •(1)Patients with urinary and reproductive tract infection, such as urethritis, prostatitis, etc.;
- •(2)Patients with diabetes and neurological diseases;
- •(3)Patients with cardiovascular diseases;
- •(4)Patients with liver and kidney dysfunction;
- •(5)Persons who abuse psychotropic drugs;
- •(6)Patients with other sexual dysfunction;
- •(7)Patients who are being treated with other drugs.
研究者
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Unknown
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