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临床试验/ITMCTR2200005669
ITMCTR2200005669尚未招募4 期

Clinical study on NIH-CPSI score of Xialiqi capsule ameliorating Type III Prostatitis ( Syndrome of Spleen-Kidney Qi Deficiency and Damp-Heat Stasis)

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

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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
18 至 50(—)
性别
Male

入选标准

  • (1) It conforms to the diagnostic criteria of Type III Prostatitis.
  • (2) It conforms to the standard of Syndrome of Spleen-Kidney Qi Deficiency and Damp-Heat Stasis.
  • (3) Aged between 18 and 50.
  • (4) NIH-CPSI=10.
  • (5) Voluntarily participate in the study and sign the informed consent.

排除标准

  • (1) Patients with type I, II and IV prostatitis.
  • (2) Those who have used drugs or other related treatments for chronic prostatitis in the past 2 weeks.
  • (3) Patients with benign prostatic hyperplasia, prostate tumor, epididymitis, seminal vesiculitis, urinary tract disease, severe neurosis diabetes, pelvic surgery history, etc.
  • (4) Patients with coronary heart disease, serious primary cardiovascular disease, liver disease, kidney disease, hematologic disease, pulmonary disease, or serious disease affecting their survival, such as tumor or AIDS, should not be selected.
  • (5) ALT, AST or BUN exceeding 2 times the upper limit of normal value, or eGFR<45ml/min/1.73m2.
  • (6) Postural hypotension.
  • (7) Non-prostatitis caused by the lower abdomen, perineum, lumbosacral and other painful diseases.
  • (8) Patients with allergic constitution or allergy to test drug composition, and patients with a history of sulfonamide drug allergy.
  • (9) Suspected or had a history of alcohol or drug abuse, or had other diseases that, according to the judgment of the investigator, reduced the possibility of enrollment or complicated enrollment, such as frequent changes in the work environment, which could easily lead to loss of follow-up.
  • (10) Patients receiving CYP3A4 or CYP2D6 potent inhibitors (such as Ketoconazole and paroxetine), other adrenergic blockers and cimetidine.
  • (11) Patients who are participating in clinical trials of other drugs, or have participated in a drug clinical trial within the past one month.
  • (12) Other patients deemed unsuitable for the clinical study by the investigator.

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