跳至主要内容
临床试验/NCT07283484
NCT07283484
招募中
不适用

Early Versus Delayed Trial Without Catheter in Men With Acute Urinary Retention: a Randomized Controlled Trial (the RELIEF Study).

Liselot Ribbert11 个研究点 分布在 1 个国家目标入组 478 人开始时间: 2025年8月21日最近更新:

概览

阶段
不适用
状态
招募中
发起方
Liselot Ribbert
入组人数
478
试验地点
11
主要终点
Re-catheterization rate after TWOC.

概览

简要总结

Acute urinary retention (AUR) is a sudden and painful condition. It occurs when a person is unable to urinate. In men, AUR is most often caused by an enlarged prostate, known as benign prostatic hyperplasia (BPH), which blocks the urethra. The first steps in treatment are to insert a catheter to empty the bladder and to start medication that acts on the prostate (an alpha-blocker). After some time, the catheter is removed during a so-called "Trial Without Catheter" (TWOC) to see whether the patient can urinate normally again.

At present, it is unclear how long a catheter should remain in place before this trial is performed. In Dutch hospitals, the duration varies widely: in some hospitals, the catheter is removed after only a few days, while in others it stays in place for two weeks or longer. A longer catheter duration can cause more discomfort and complications, such as urinary tract infections or blood in the urine. Therefore, it is important to determine whether a shorter catheterization period is equally effective and safe compared to a longer one.

The RELIEF study investigates whether a short catheter duration of three days is as safe and effective as the current average of fourteen days. A total of 478 men with acute urinary retention will participate in this nationwide randomized controlled trial. All participants will receive a catheter and start (or continue) treatment with an alpha-blocker. They will then be randomly assigned to one of two groups: one group will have the catheter removed after three days, and the other group after fourteen days.

The main question is whether a shorter catheter duration is as successful as a longer one. Success means that the patient can urinate normally after catheter removal, without needing to have the catheter replaced. The study will also compare the number of complications, patients' experiences with the catheter, their quality of life, and the overall healthcare costs.

By conducting this study, doctors will gain better evidence on the optimal timing of catheter removal in men with AUR. The goal is to avoid unnecessarily long catheterization, reduce discomfort and complications, and improve the quality of care for men with AUR. The results of the RELIEF study may help improve the management of AUR, making care more consistent, efficient, and patient-friendly both in the Netherlands and abroad.

详细描述

not aplicable

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 (Outcomes Assessor)

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

  • Adult men (≥18 years)
  • Diagnosis of acute urinary retention (AUR) treated with a transurethral catheter (TUC) and alpha-blocker therapy (tamsulosin, silodosin, or alfuzosin)
  • Mentally competent and able to understand the potential benefits and burdens of study participation
  • Provision of written or digital informed consent

排除标准

  • Failed prior TWOC within the preceding 30 days
  • Initial urinary retention volume \>1500 mL
  • Neurogenic bladder dysfunction (e.g., multiple sclerosis, spinal cord injury, spina bifida)
  • History of prostate cancer with ISUP grade group ≥2
  • History of active bladder cancer or ongoing surveillance for bladder cancer
  • Urinary retention occurring within 72 hours after surgery (postoperative urinary retention)
  • History of lower urinary tract surgery (e.g., bladder augmentation, urethral surgery, or prostate surgery)
  • AUR suspected to be caused by bladder stones
  • Suspected urethral stricture, clot retention, or urosepsis
  • Contraindication to alpha-blocker therapy

结局指标

主要结局

Re-catheterization rate after TWOC.

时间窗: Either 3 or 14 days after catheterization, depending on study group allocation.

次要结局

  • Patient reported outcomes - ICIQ-LTCqol(Days 3 and 12 after catheter insertion, and at 1, 2, 3, and 6 months.)
  • Patient reported outcomes - IPSS(Days 3 and 12 after catheter insertion, and at 1, 2, 3, and 6 months.)
  • Patient reported outcomes - EQ-5D-5L(Days 3 and 12 after catheter insertion, and at 1, 2, 3, and 6 months.)
  • Process related outcomes - Catheter-related complications(Up to 18 months after catheter insertion.)
  • Resource related outcomes - Productivity losses(Up to 6 months after catheter insertion (iPCQ assessed at 1, 2, 3, and 6 months).)
  • Resource related outcomes - Health care costs(Up to 6 months after catheter insertion (iMCQ assessed at 3 and 6 months).)

研究者

发起方
Liselot Ribbert
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Liselot Ribbert

Study Director

Isala

研究点 (11)

Loading locations...

相似试验