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临床试验/NCT00919477
NCT00919477已完成不适用

Protocol for the Specified Clinical Experience Investigation on the Single Use of Casodex® Tablet 80 mg

AstraZeneca1 个研究点 分布在 1 个国家目标入组 712 人开始时间: 2009年5月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
AstraZeneca
入组人数
712
试验地点
1
主要终点
Adverse event incidence

研究概览

简要总结

To gather information on the safety of monotherapy of Casodex® tablets 80 mg, targeting prostate cancer patients who have no history of having received treatment by either endocrine therapy (including surgical castration).

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

性别
Male
接受健康志愿者

入选标准

  • Prostate cancer patients who have no history of receiving endocrine therapy (including surgical castration), and who plan to undergo Casodex® tablets monotherapy for not less than 12 months

排除标准

  • 未提供

结局指标

主要结局

Adverse event incidence

时间窗: Time since starting Casodex monotherapy, monthly

次要结局

  • improvement of prostate cancer using Tumor marker PSA(Time since starting Casodex monotherapy, monthly)
  • Maintenance of sexual function(At 3 months since starting Casodex monotherapy,)

研究者

发起方
AstraZeneca
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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