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临床试验/NCT03239951
NCT03239951终止不适用

One-arm, Controlled, Multi-Center Prospective Study to Assess the Efficacy, Safety and Tolerability of Medi-Tate Temporary Implantable Nitinol Device (iTind) in Subjects With Acute Urinary Retention Secondary to (BPO)

Medi-Tate Ltd.4 个研究点 分布在 1 个国家目标入组 5 人开始时间: 2018年2月27日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
5
试验地点
4
主要终点
Ability to void without catheter

研究概览

简要总结

Subjects with AUR secondary to BPO that comply with Inclusion/Exclusion Criteria.

A total of 50 eligible subjects will be recruited into the study to receive treatment with iTind system.

Study duration will be 12 months post implantation, with follow-up extension of up to 3 years. Extension of follow up period will not require an additional ICF.

详细描述

Spontaneous acute urinary retention (AUR) is one of the most significant complications of long-term benign prostatic hyperplasia (BPH). In the past it has represented an immediate indication for surgery. Between 25% and 30% of men who underwent transurethral prostatectomy (TURP) had AUR as their main indication in older series and today most subjects failing to void after attempted catheter removal still undergo surgery. For this reason alone, AUR is an important and feared event from the viewpoint of the subject. The subject originally has inability to urinate, with increasing pain, and eventually a visit to the emergency room, catheterization, follow-up visits to the physicians, an attempt at catheter removal, and eventual recovery or surgery, which is both painful and time consuming.

After the acute period most men with AUR will be offered a 'trial without catheter' (TWOC) and about half will resume spontaneous voiding. Most men who fail a TWOC, experience a recurrent episode of AUR, or have moderate or severe lower urinary tract symptoms (LUTS) that are refractory to medical management will be considered for surgery.

In the older literature, the risk of recurrent AUR was cited as 56% to 64% within 1 week of the first episode and 76% to 83% in men with diagnosed BPH.

(http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1476058/). Additional researches show that ten percent of men in their seventies and 30% in their eighties will have AUR within the next five years.

Benign prostatic hyperplasia is the cause for the AUR in at least 65% of men presenting with AUR.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
40 Years 至 90 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Male with AUR secondary to BPO
  • Age ≥40 years
  • Acute urinary retention with at least one failed trial without catheter (TWOC) while on alpha blocker
  • Ability to sign an informed consent form
  • Prostate volume <80 ml
  • Life expectancy >1 year.

排除标准

  • Suspected malignant disease of the lower urinary tract including prostate or bladder cancer
  • Chronic retention of urine with history of either retention volume greater than one liter or upper tract obstruction
  • Known neurogenic bladder
  • Immunosuppression
  • Suspected urethral strictures, bladder neck contracture, Urinary bladder stones
  • An obstructive or protruding median lobe of the prostate
  • An active symptomatic urinary tract infection
  • Enrolled in another treatment trial for any disease
  • Previous pelvic irradiation or radical pelvic surgery
  • Any previous prostate surgery.

结局指标

主要结局

Ability to void without catheter

时间窗: 2 weeks

TWOC Success Rate, defined as the proportion (%) of subjects successfully undergoing the TWOC assessment at the later of visit 3 or visit 4.

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (4)

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