跳至主要内容
临床试验/NCT00316732
NCT00316732已完成不适用

Observational Sutdy to Assess the Effectiveness of Avodart in Subjects With Benign Prostatic Hyperplasia in Day to Day Clinical Practice

GlaxoSmithKline1 个研究点 分布在 1 个国家目标入组 173 人开始时间: 2004年10月25日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
173
试验地点
1

研究概览

简要总结

This study was designed to assess the effectiveness of dutasteride in the actual clinical practice of prostate assessment clinics in the UK in accordance with best practice over a 12-month period.

研究设计

研究类型
Observational
时间视角
Prospective

入排标准

性别
Male
接受健康志愿者

入选标准

  • Patients who not have received any pharmacological treatment or surgical interventions for BPH (Benign Prostatic Hyperplasia).
  • Patients should be prescribed dutasteride in compliance with the UK SmPC and BAUS guidelines on the treatment of BPH.
  • Patients must only enter the study after the decision to prescribe dutasteride has been undertaken.
  • Exclusion criteria: None specified

排除标准

  • 未提供

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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