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临床试验/NCT06540248
NCT06540248已完成不适用

Real-life Clinical Experience With a Minimally Invasive Syringe Adapter for Catheter Free Instillation of Intravesical Treatments

Radboud University Medical Center1 个研究点 分布在 1 个国家目标入组 61 人开始时间: 2023年11月1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
61
试验地点
1
主要终点
Number of participants who reported success (in using syringe adapter) Yes/No

研究概览

简要总结

A retrospective study from a single center was performed. Quantitative and qualitative data was obtained on the use of the syringe adapter (IALUADAPTER®) in 61 patients with IC/BPS (n=48), rUTI (n=6) and mixed /other diagnoses (including OAB; n= 7) who were receiving intravesical therapy. The evaluation period was 6 months during 2018-2019. Reasons for trying the syringe adapter, reasons for continuing with it and occurrence of UTIs before and during the evaluation period were recorded. In addition, 3 year follow-up data were obtained to assess long-term usage of the syringe adapter.

详细描述

Introduction Intravesical treatment is currently dependent on catheterization which can cause urethral discomfort and risk of urinary tract infections in selected patient groups such as interstitial cystitis / bladder pain syndrome (IC/BPS), overactive bladder syndrome (OAB) and recurrent urinary tract infections (rUTI). This study describes real-life clinical experience of a minimally invasive syringe adapter (Ialudapter®) for catheter-free instillation of intravesical treatment.

Methods A retrospective study from a single center was performed. Quantitative and qualitative data was obtained on the use of the syringe adapter (IALUADAPTER®) in 61 patients with IC/BPS (n=48), rUTI (n=6) and mixed /other diagnoses (including OAB; n= 7) who were receiving intravesical therapy. The evaluation period was 6 months during 2018-2019. Reasons for trying the syringe adapter, reasons for continuing with it and occurrence of UTIs before and during the evaluation period were recorded. In addition, 3 year follow-up data were obtained to assess long-term usage of the syringe adapter.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

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

入选标准

  • Patients with IC/BPS, recurrent UTIs and/or OAB
  • Receiving intravesical instillations with a conventional single-use catheter before the syringe adapter evaluation period which took place between September 2018 and the end of February 2019 (6m).

排除标准

  • Patients with a high post-void residue of >100ml or with an indwelling catheter were excluded from the analyses.
  • Patients who cannot sign informed consent.

结局指标

主要结局

Number of participants who reported success (in using syringe adapter) Yes/No

时间窗: 6 months

pt self reported general assessment of successful instillation using the syringe adapter

次要结局

  • Number of participants who use syringe adapter 3 years after initial assessment (yes/no)(1 yr)
  • Total number of UTI's during syringe adapter use amongst all patients(6 months)
  • PRO; patient reported reasons for trying syringe adapter in stead of regular catheter (5 options)(6 months)
  • PRO ; patient reported reasons to continue syringe adapter (5 options)(6 months)

研究者

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

Dick Janssen

MD PhD

Radboud University Medical Center

研究点 (1)

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