NCT00771264已完成4 期
Study of Urgent PC Versus Sham Effectiveness in Treatment of Overactive Bladder Symptoms
适应症
干预措施
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 220
- 试验地点
- 15
- 主要终点
- The Global Response Assessment (GRA) for Overall Bladder Symptoms to Compare the Proportion of Subjects Reporting "Moderately" or "Markedly Improved" Responses on the GRA After 12 Interventions of Randomized Therapy, in an Intent to Treat Analysis.
研究概览
简要总结
The purpose of this study is to demonstrate superiority of percutaneous posterior tibial nerve stimulation (PTNS) therapy compared to sham therapy for the treatment of patients with overall bladder (OAB) symptoms.
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
- Double (Participant, 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
- 是
入选标准
- •Women and men >18 years of age
- •A score of > 4 on the OAB-q short form for urgency (question 1)
- •Average urinary frequency > 10 times in one 24 hour day based on a 3-day voiding diary
- •Self-reported bladder symptoms present > 3 months
- •Self-reported failed conservative care (i.e., dietary restriction, fluid restriction, bladder training, behavioral modification, pelvic muscle training, biofeedback, etc.)
- •Off all antimuscarinics for at least 2 weeks prior to enrollment
- •Capable of giving informed consent
- •Ambulatory and able to use a toilet independently, without difficulty
- •Capable and willing to follow all study-related procedures
排除标准
- •Pregnant as confirmed by urine pregnancy test, or plans to become pregnant during the study period
- •Neurogenic bladder
- •Botox use in bladder or pelvic floor muscles in the past year
- •Pacemakers or implantable defibrillators
- •Primary complaint of stress urinary incontinence
- •Current urinary tract infection (UTI)
- •Current vaginal infection
- •Current use of InterStim
- •Current use of Bion
- •Current use of TENS in the pelvic region, back or legs
- •Previously been treated with PTNS
- •Use of investigational drug/device therapy within the past 4 weeks
- •Participating or have participated within the past 4 weeks in any clinical investigation involving or impacting gynecologic, urinary or renal function
- •Deemed unsuitable for enrollment in study by the investigators based on subjects' history or physical examination (including bleeding disorders or anticoagulant medications, and peripheral neuropathy)
- •Subjects with nerve damage that would impact either percutaneous tibial nerve or pelvic floor function
研究组 & 干预措施
Urgent PC
Active Comparator
干预措施: Urgent PC Neuromodulation System (Device)
Sham / Placebo
No Intervention
结局指标
主要结局
The Global Response Assessment (GRA) for Overall Bladder Symptoms to Compare the Proportion of Subjects Reporting "Moderately" or "Markedly Improved" Responses on the GRA After 12 Interventions of Randomized Therapy, in an Intent to Treat Analysis.
时间窗: 13 weeks
A responder was defined as reporting bladder symptoms as moderately or markedly improved on a 7-level GRA at week 13 after completing 12, 30-minute, consecutive weekly intervention sessions.
次要结局
未报告次要终点
研究者
研究点 (15)
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