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临床试验/ITMCTR2200005688
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)

Xiyuan Hospital of China Academy of Chinese Medical Sciences0 个研究点开始时间: 待定最近更新:
适应症

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简要总结

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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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