跳至主要内容
临床试验/NCT00392002
NCT00392002已完成4 期

A Cluster-Randomized Study to Examine National Characteristics and Outcome Measures of GERD Patients Utilizing the PPI Acid Suppression Symptom (PASS) Test for Response [EncomPASS].

AstraZeneca2 个研究点 分布在 1 个国家目标入组 2,000 人开始时间: 2005年10月1日最近更新:
适应症
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
AstraZeneca
入组人数
2,000
试验地点
2
主要终点
To compare the improvement in burden of overall GERD symptoms after 4 weeks of treatment with Esomeprazole verses maintenance of current therapy in subjects with persistent GERD symptoms.

研究概览

简要总结

To characterize the burden of disease in GERD patients of prescription therapy'

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
None

入排标准

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

入选标准

  • •Signed informed consent, 18 years or older, diagnosis of GERD

排除标准

  • •Peptic ulcer disease, upper gastrointestinal surgery, malignancy

结局指标

主要结局

To compare the improvement in burden of overall GERD symptoms after 4 weeks of treatment with Esomeprazole verses maintenance of current therapy in subjects with persistent GERD symptoms.

次要结局

  • To examine the relationship of the severity and frequency of GERD symptoms to treatment, at national, and regional levels.

研究者

发起方
AstraZeneca
申办方类型
Industry

研究点 (2)

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