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临床试验/NCT00332319
NCT00332319终止2 期

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GlaxoSmithKline4 个研究点 分布在 1 个国家目标入组 1 人开始时间: 2006年1月1日最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
终止
入组人数
1
试验地点
4
主要终点
Change in bladder nerve activity assessed by neurometry before and after a single dose of GW679769 and placebo (part A) and after 28 days of drug or placebo treatment (part B).

研究概览

简要总结

This is a two-part study in which Part A will assess the effects of GW679769 after 1 dose on the function of the nerves that supply the bladder. The technique for measuring the nerves function is called Neurometry. Part B will assess the effect of repeat doses of GW679769 on the bladder nerve function. Part B will also assess the effects of the drug on overactive bladder symptoms using a three-day patient diary.

详细描述

A randomized, double-blind, placebo-controlled study to evaluate the effects of GW679769 on Current Perception Threshold (CPT) following a single 150 mg dose (Part A) and to evaluate the effect of CPT and symptoms of overactive bladder following 28 days of repeat dosing with 120 mg GW679769 administered once daily (Part B) in patients with neurogenic bladder due to incomplete spinal cord injury

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Double

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Spinal cord injury patients with overactive bladder symptoms including urge incontinence, urgency, frequency and night-time urination but without bladder related pain.
  • The injury must be above S1-3

排除标准

  • Spinal cord injury suffered within 6 months.
  • History of interstitial cystitis, radiation cystitis, pelvic irradiation, or myocardial infarction with 1 year prior to screening.
  • Pregnant or nursing females.
  • Patients who have had hypersensitivity to lidocaine.
  • Patients who are taking oral corticosteroids.
  • Patients with active peptic ulcer disease (PUD) and/or history of PUD of an unknown etiology.

结局指标

主要结局

Change in bladder nerve activity assessed by neurometry before and after a single dose of GW679769 and placebo (part A) and after 28 days of drug or placebo treatment (part B).

次要结局

  • Improvement of OAB symptoms (incontinence, frequency of urination, reduction in urgency, decrease in night-time urination episodes).

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (4)

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