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临床试验/NCT00284518
NCT00284518已完成2 期

Safety and Efficacy Study of Botulinum Toxin Type A to Treat Lower Urinary Symptoms Due to Benign Prostatic Hyperplasia

Allergan0 个研究点目标入组 380 人开始时间: 2005年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
Allergan
入组人数
380
主要终点
Change From Baseline in International Prostate Symptom Score (IPSS) at Week 12

研究概览

简要总结

The purpose of this study was to determine the safety and effectiveness of different doses of botulinum toxin Type A in treating lower urinary tract symptoms due to benign prostatic hyperplasia.

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
50 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Lower urinary tract symptoms due to benign prostatic hyperplasia
  • Enlarged prostate volume by rectal ultrasound

排除标准

  • Previous prostate surgery
  • Previous or current diagnosis of prostate cancer
  • Use of other medications for the treatment of prostatic hyperplasia
  • Urinary tract infection

研究组 & 干预措施

botulinum toxin Type A 100 U

Experimental

Botulinum toxin Type A 100 U transperineal or transrectal injection on Day 1.

干预措施: botulinum toxin Type A (Biological)

botulinum toxin Type A 300 U

Experimental

Botulinum toxin Type A 300 U transperineal or transrectal injection on Day 1.

干预措施: botulinum toxin Type A (Biological)

botulinum toxin Type A 200 U

Experimental

Botulinum toxin Type A 200 U transperineal or transrectal injection on Day 1.

干预措施: botulinum toxin Type A (Biological)

Placebo (Normal Saline)

Placebo Comparator

Placebo (Normal Saline) transperineal or transrectal injection on Day 1.

干预措施: normal saline (Drug)

结局指标

主要结局

Change From Baseline in International Prostate Symptom Score (IPSS) at Week 12

时间窗: Baseline, Week 12

The International Prostate Symptom Score is a disease-specific outcome measure based on the American Urological Association Symptom Index. The questionnaire consists of seven items. The patient evaluates their urinary symptoms (incomplete emptying, frequency, hesitancy, urgency, weak stream, straining, and nocturia) during the previous 4 weeks. The total symptom score can range from 0 (no symptoms) to 35 (most severe symptoms). A negative change from baseline indicates improvement.

次要结局

  • Change From Baseline in International Prostate Symptom Score (IPSS) at Week 72(Baseline, Week 72)
  • Change From Baseline in Peak Urine Flow Rate(Baseline, Week 12, Week 72)
  • Change From Baseline in Total Prostate Volume(Baseline, Week 12, Week 72)
  • Change From Baseline in Transitional Zone Prostate Volume(Baseline, Week 12, Week 72)
  • Change From Baseline in Post-Void Residual(Baseline, Week 2, Week 12, Week 72)

研究者

发起方
Allergan
申办方类型
Industry
责任方
Sponsor

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