ACTRN12613000167763进行中（未招募）未知
Single-arm prospective, interventional pilot study to evaluate the safety, feasibility and efficacy of the PROCEPT AquablationTM System (PAS) device for the treatment of Benign Prostatic Hyperplasia (BPH)
试验速览
- 阶段
- 未知
- 状态
- 进行中（未招募）
- 入组人数
- 30
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomised trial
- 主要目的
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 50 Years 至 o limit（—）
- 性别
- Male
入选标准
- •Male, Age > 50 years with BPH and history of inadequate response to medical therapy.
排除标准
- •Large median lobe, urethral length >6cm, prostates >80g, prostate cancer, current urological conditions affecting procedural outcomes, previous prostate surgery, significant renal impairment, listed concomitant medications and listed uncontrolled co-morbidities.
研究者
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