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临床试验/NCT04566588
NCT04566588已完成不适用

Early Apical Release vs Classic Holmium Laser Enucleation of the Prostate: Randomized Controlled Trial Comparing Post-Operative Incontinence Rates and Surgical Outcomes

University of Kansas Medical Center2 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2020年6月25日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
12
试验地点
2
主要终点
Post-operative Urinary Incontinence

研究概览

简要总结

To determine if early apical release holmium enucleation of the prostate (EAR HoLEP), as a surgical treatment for benign prostatic hyperplasia, reduces post-operative urinary incontinence compared to classic HoLEP.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Patients must be 18 years of age or older
  • Patients must present to clinic with a diagnosis of benign prostatic hyperplasia
  • Patients must be scheduled to undergo a holmium laser enucleation of the prostate

排除标准

  • Patients with previous surgical management of BPH
  • Patients with prostate biopsy revealing high risk prostate cancer
  • Patients with a concomitant neurogenic bladder diagnosis (SCI, Parkinson, MS, cerebral palsy)

结局指标

主要结局

Post-operative Urinary Incontinence

时间窗: Twelve Months Post-operative

to determine if patients who undergo early apical release HoLEP have reduced rates of post-operative urinary incontinence compared to classic HoLEP as measured by patient report of leakage

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Don Neff, MD, FACS

Associate Professor

University of Kansas Medical Center

研究点 (2)

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