跳至主要内容
临床试验/NCT00311376
NCT00311376已完成3 期

Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Neurogenic Overactive Bladder

Allergan14 个研究点 分布在 14 个国家目标入组 416 人开始时间: 2006年8月1日最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
已完成
发起方
Allergan
入组人数
416
试验地点
14
主要终点
Change From Baseline in Number of Weekly Episodes of Urinary Incontinence

研究概览

简要总结

The purpose of this study is to assess the safety and effectiveness of botulinum toxin type A in treating overactive bladder in spinal cord injury or multiple sclerosis patients.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Urinary incontinence as a result of neurogenic overactive bladder due to spinal cord injury or multiple sclerosis
  • Inadequate response to anticholinergic medication used to treat overactive bladder

排除标准

  • History of evidence of pelvic or urologic abnormality
  • Previous or current diagnosis of bladder or prostate cancer
  • Urinary tract infection at time of enrollment

研究组 & 干预措施

1

Experimental

botulinum toxin Type A (200U)

干预措施: botulinum toxin Type A (200U) (Biological)

2

Experimental

botulinum toxin Type A (300U)

干预措施: botulinum toxin Type A (300U) (Biological)

3

Other

placebo; botulinum toxin Type A (200U)

干预措施: Normal Saline (Placebo); botulinum toxin Type A (200U) (Other)

4

Other

placebo; botulinum toxin Type A (300U)

干预措施: Normal Saline (Placebo); botulinum toxin Type A (300U) (Other)

结局指标

主要结局

Change From Baseline in Number of Weekly Episodes of Urinary Incontinence

时间窗: Baseline, Week 6

Change from baseline in the weekly frequency of incontinence episodes at Week 6 after the first treatment. Incontinence is defined as involuntary loss of urine as recorded in a patient bladder diary. A negative number change from baseline indicates a reduction in incontinence episodes (improvement).

次要结局

  • Change From Baseline in Maximum Cystometric Capacity (MCC)(Baseline, Week 6)
  • Change From Baseline in Maximum Detrusor Pressure (MDP)(Baseline, Week 6)
  • Change From Baseline in Total Score on Incontinence Quality of Life (I-QOL) Questionnaire(Baseline, Week 6)

研究者

发起方
Allergan
申办方类型
Industry
责任方
Sponsor

研究点 (14)

Loading locations...

相似试验

Safety and Efficacy Study of Botulinum Toxin Type A... | 临床试验