跳至主要内容
临床试验/NCT06385769
NCT06385769尚未招募不适用

Efficacy of Transcutaneous Tibial Nerve Stimulation in Patients With Neurogenic Overactive Bladder After Stroke: A Randomized Placebo-controlled Clinical Trial.

Pamukkale University2 个研究点 分布在 2 个国家目标入组 22 人开始时间: 2024年4月22日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
22
试验地点
2
主要终点
Decreased frequency of increased voiding

研究概览

简要总结

The investigators conducted a prospective, randomized, double-blind, placebo-controlled study based on the placebo technique to evaluate the efficacy of TTNS versus placebo in patients with OAB after stroke.

The main questions aimed to be answered are:

What are the effects of Trans Tibial Nerve Stimulation (TTNS) on incontinence-related clinical parameters and quality of life in patients with overactive bladder (OAB) after stroke compared to the placebo group? Participants (n:22) with post-stroke AAM who meet the exclusion and inclusion criteria will be divided into 2 groups using a randomization table. The first group will receive TTNS (n:11) and the second group will receive placebo TTNS (n:11). Measurements will be performed twice in total, before treatment and at the end of treatment (4th week).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Triple (Participant, Investigator, Outcomes Assessor)

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 aged 40 and above with stable ischemic or hemorrhagic stroke.
  • Patients with neurogenic detrusor overactivity symptoms accompanied by urinary incontinence complaints and a urinary frequency of 9 or more.
  • Patients diagnosed with detrusor overactivity on urodynamic evaluation.
  • Patients with hemiplegia lasting between 30 days and 1 year.
  • Ability to understand procedures, benefits, and potential side effects.
  • Patients scoring 22 or above on the Mini Mental Test.

排除标准

  • Patients with post-stroke neurogenic detrusor overactivity receiving or previously received pharmacological treatment.
  • Patients using intermittent catheterization or permanent catheterization as a bladder emptying method.
  • Patients with a history of urinary incontinence and/or urinary retention before stroke.
  • History of past urogynecological surgery.
  • Presence of urinary tract infection, bladder tumor, or cardiac pacemaker.
  • Significant fluid infusion requirement affecting urination or use of medication affecting bladder function.
  • Patients who have received botulinum toxin injection for post-stroke neurogenic detrusor overactivity.
  • Patients with postvoid residual volume above 150 mL.

结局指标

主要结局

Decreased frequency of increased voiding

时间窗: Change from baseline positive response rate at the 4th week after the treatment

The effectiveness of the treatment is evaluated based on the daily voiding frequency post-treatment compared to the daily voiding frequency pre-treatment. The expected outcome is a reduction in the frequency of increased voiding.

次要结局

  • Frequency of voiding(Change from baseline Frequency of voiding, nocturia, number of pads at the 4th week after the treatment)
  • The Quality of Life(Change from baseline the Quality of Life at the 4th week after the treatment)
  • Barthel Index for Activities of Daily Living (ADL)(Change from baseline Barthel Index for Activities of Daily Living at the 4th week after the treatment)
  • The Overactive Bladder Symptom Score (OABSS)(Change from baseline The Overactive Bladder Symptom Score at the 4th week after the treatment)
  • Treatment Satisfaction Level(Change from baseline Treatment Satisfaction Level at the 4th week after the treatment)
  • Cystometric value(Change from baseline Cystometric value at the 4th week after the treatment)

研究者

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

Necmettin Yildiz

Professor Doctor

Pamukkale University

研究点 (2)

Loading locations...

相似试验