跳至主要内容
临床试验/NCT02245503
NCT02245503已完成不适用

Comorbidity and Comedication During Prescription of ALNA® (Tamsulosin) for Patients With BPH (Benign Prostatic Hyperplasia)

Boehringer Ingelheim0 个研究点目标入组 7,391 人开始时间: 2003年5月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
7,391
主要终点
Collection of information on concomitant diseases

研究概览

简要总结

The objectives of this post marketing surveillance study were to document the comorbidity and comedication during prescription of ALNA® (Tamsulosin) for patients with BPH (Benign Prostatic Hyperplasia).

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

  • Indication for the treatment with ALNA according to its summary of product characteristics (SPC)

排除标准

  • Patients fulfilling one of the general or specific contraindications listed in the ALNA SPC, particularly patients with known hypersensitivities against tamsulosin hydrochloride or any other ingredient of the product, orthostatic dysregulation or severe liver insufficiency cannot be included in the study

研究组 & 干预措施

Benign prostatic hyperplasia

Patients with symptomatic BPH to whom ALNA was prescribed

干预措施: Tamsulosin (Drug)

结局指标

主要结局

Collection of information on concomitant diseases

时间窗: day 1

Collection of information on concomitant treatment

时间窗: day 1

次要结局

  • Number of patients with adverse drug reactions(up to 6 months)

研究者

申办方类型
Industry
责任方
Sponsor

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