JPRN-jRCTs071190040进行中(未招募)未知
Evaluation of selective beta3-adrenoreceptor agonist vibegron treatment for residual overactive bladder symptoms after photoselective, contact-laser, and thulium-laser vaporization of the prostate: A single-centre randomized controlled trial (VAPOR trial)
Seki Narihito0 个研究点目标入组 60 人开始时间: 2020年1月8日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 60
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- >= 40age old 至 ot applicable(—)
- 性别
- Male
入选标准
- •1) Male patients >= 40 years
- •2) Patient who has passed 12 weeks or more and less than 1 year after PVP,CVP or ThuVAP for BPH at the time of obtaining written informed consent
- •3)Patient with an IPSS-QOL score >= 2
- •4) Patient with a OABSS >= 3, a OABSS question1 score >=1 and a OABSS question3 score >= 2
- •5) Patient who can record a bladder diary
- •6) Patient with an average urinary frequency of 8 times or more per day at baseline (0 week)
- •7) Patient who provided written informed consent
排除标准
- •1) Patient has post-void residual volume >= 100mL
- •2) Patient who is placed a catheter for a long time after undergoing PVP,CVP orThuVAP,or those who is utilizing a self -catheterization for bladder management
- •3)Patient has a complication with symptoms similar to OAB ( e g diabetes insipidus, urolithiasis, urinary tract infection, interstitial bladder cystitis, prostatitis) and patient who is judged affectable for enrollment by principle investigator or sub investigator
- •4) Patient with only stress incontinence
- •5) Patient has a history of injury, surgery or multiple sclerosis that could affect the lower urinary tract or its
- •nerve supply
- •6)Patients with bladder or prostate cancer and undergoing or scheduled radiation therapy
- •7) Patient who is receiving a medication therapy and or a behavioral therapy for OAB at enrollment
- •8) Patient who has received a drug that affect lower urinary tract symptoms ( e g alpha1 blocker, PDE5 inhibitor, anticholinergic agent or beta-adrenergic receptor agonist) within the last 2 months
- •9) Patient who received 5alpha-reductase inhibitor within the last 3 months
- •10) Patient who is judged unsuitable for enrollment by principle investigator or sub investigator
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