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临床试验/ITMCTR2100004596
ITMCTR2100004596招募中4 期

Efficacy and safety of Qianlieshutong capsule in the treatment of type III prostatitis (TCM syndrome of damp-heat and blood-stasis obstruction): a multicenter, randomized, double-blind, single simulation, positive drug parallel controlled clinical trial

Beijing Hospital0 个研究点开始时间: 待定最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
发起方

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
18 至 50(—)
性别
Male

入选标准

  • 1. The diagnosis criterias of type III prostatitis are met;
  • 2. The diagnosis criterias of TCM syndrome of damp-heat and blood-stasis obstruction are met;
  • 3. Aged >= 18 and <= 50 years;
  • 4. Chronic prostatitis symptom index (NIH CPSI) is more than 10, and pain score was >= 4;
  • 5. Patients sign informed consent voluntarily.

排除标准

  • 1. Patients have weak waist and knees and are afraid of cold;
  • 2. Patients diagnosed of benign prostatic hyperplasia, acute urinary retention, urethral stricture, epididymitis, seminal vesicle inflammation, severe neurosis, sexually transmitted diseases, bladder tumor, prostate cancer, and urinary male reproductive system tuberculosis;
  • 3. Patients with pain diseases of lower abdomen, perineum, lumbosacral and other parts caused by non prostatitis;
  • 4. Patients with severe cardiovascular, cerebrovascular, liver and kidney, endocrine system, hematopoietic system, mental and nervous system and other primary diseases, liver function ALT and / or AST were 1.5 times higher than the upper limit of normal value, and renal function (CR) was greater than the upper limit of normal value;
  • 5. Suspected or confirmed history of alcohol and drug abuse;
  • 6. Urinary tract infection;
  • 7. Refractory patients treated with a - blockers;
  • 8. Postural hypotension patients;
  • 9. Allergic to the trial drug and its components;
  • 10. Patients who had pelvic surgery within 3 months;
  • 11. Patients who have used drugs or other related treatment for chronic prostatitis in recent 2 weeks;
  • 12. Patients who have participated in other clinical trials in recent 3 months;
  • 13. Patients who have birth planning during the period of medication and within one month after the end of medication;
  • 14. Patients who are considered unsuitable for clinical trials by researchers.

研究者

发起方
Beijing Hospital

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