ITMCTR1900002519招募中未知
Evaluation for Clinical Efficacy of Anatomical Enucleation of the Prostate for the Treatment of Benign Prostatic Hyperplasia with Underactive bladder
Guangdong Provincial Hospital of Chinese Medicine0 个研究点开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 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
- Observational study
入排标准
- 年龄范围
- 60 至 80(—)
- 性别
- Male
入选标准
- •1. Aged 60-80 years, men;
- •2. Diagnosis of benign prostatic obstruction; Urodynamics suggest weak or no contraction of the detrusor(BCI<100 or Pdet@Qmax<40cmH2O)
- •3. With any of the following conditions:
- •(1) The International Prostate Symptom Score (IPSS>=12), and the quality of life score (QOL)>=4 points;
- •(2) The maximum urinary flow rate (Qmax) is less than 15ml/s (>=150ml);
- •(3) The effect of drug treatment is not good;
- •(4) The recurrent urinary retention (more than once);
- •4. Subject is classified ASA I, II, or III;
- •5. The patient agreed to participate in this trial, and signed informed consent.
排除标准
- •1. There is operation contraindications of transurethral prostatic hyperplasia resection;
- •2. Subject has a life expectancy <2 yr;
- •3. Subject is currently enrolled in or plans to enrol in any other study;
- •4. Subject has a Normal detrusor contractility;
- •5. Subject has diagnosis of stress urinary incontinence that requires treatment or daily pad or device use;
- •6. Subject has history urethral stricture or bladder neck contracture within the last 6 months;
- •7. Subject has history of lower urinary tract surgery;
- •8. Subject has diagnosis of prostate cancer;
- •9. Combined with advanced malignant tumor or chronic wasting disease;
- •10. Combined with serious heart,lung disease or severe mental disorder;
- •11. Has an active infection;
- •12. Subject has a disorder of the coagulation cascade or disorders that affect platelet count or function;
- •13. Can not finished the follow-up for poor compliance.
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