Tiotropium in the Treatment of the Patients With Chronic Obstructive Pulmonary Disease (COPD)
2014年6月26日 更新者:Boehringer Ingelheim
Drug Use Results Survey of Tiotropium Bromide
To collect post-marketing safety and effectiveness information on the use of Tiotropium Inhalation Capsules (18 μg) in patients with chronic obstructive pulmonary disease in daily clinical settings
研究概览
研究类型
观察性的
注册 (实际的)
3588
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
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Toyooka、日本
- Boehringer Ingelheim Investigational Site
-
Toyosatocho、日本
- Boehringer Ingelheim Investigational Site
-
Toyota、日本
- Boehringer Ingelheim Investigational Site
-
Tsu、日本
- Boehringer Ingelheim Investigational Site
-
Tsukuba、日本
- Boehringer Ingelheim Investigational Site
-
Tsurugicho、日本
- Boehringer Ingelheim Investigational Site
-
Tsuruoka、日本
- Boehringer Ingelheim Investigational Site
-
Tsushima、日本
- Boehringer Ingelheim Investigational Site
-
Tsuyama、日本
- Boehringer Ingelheim Investigational Site
-
Ube、日本
- Boehringer Ingelheim Investigational Site
-
Uchikocho、日本
- Boehringer Ingelheim Investigational Site
-
Uchinadamachi、日本
- Boehringer Ingelheim Investigational Site
-
Uekimachi、日本
- Boehringer Ingelheim Investigational Site
-
Uji、日本
- Boehringer Ingelheim Investigational Site
-
Uki、日本
- Boehringer Ingelheim Investigational Site
-
Unzen、日本
- Boehringer Ingelheim Investigational Site
-
Urakawacho、日本
- Boehringer Ingelheim Investigational Site
-
Urasoe、日本
- Boehringer Ingelheim Investigational Site
-
Urayasu、日本
- Boehringer Ingelheim Investigational Site
-
Uruma、日本
- Boehringer Ingelheim Investigational Site
-
Usa、日本
- Boehringer Ingelheim Investigational Site
-
Usuki、日本
- Boehringer Ingelheim Investigational Site
-
Utsunomiya、日本
- Boehringer Ingelheim Investigational Site
-
Wakayama、日本
- Boehringer Ingelheim Investigational Site
-
Yabu、日本
- Boehringer Ingelheim Investigational Site
-
Yachimata、日本
- Boehringer Ingelheim Investigational Site
-
Yachiyo、日本
- Boehringer Ingelheim Investigational Site
-
Yaizu、日本
- Boehringer Ingelheim Investigational Site
-
Yakumocho、日本
- Boehringer Ingelheim Investigational Site
-
Yakushimacho、日本
- Boehringer Ingelheim Investigational Site
-
Yamaga、日本
- Boehringer Ingelheim Investigational Site
-
Yamagata、日本
- Boehringer Ingelheim Investigational Site
-
Yamato、日本
- Boehringer Ingelheim Investigational Site
-
Yamatotakada、日本
- Boehringer Ingelheim Investigational Site
-
Yanai、日本
- Boehringer Ingelheim Investigational Site
-
Yao、日本
- Boehringer Ingelheim Investigational Site
-
Yatomi、日本
- Boehringer Ingelheim Investigational Site
-
Yatsushiro、日本
- Boehringer Ingelheim Investigational Site
-
Yawata、日本
- Boehringer Ingelheim Investigational Site
-
Yokkaichi、日本
- Boehringer Ingelheim Investigational Site
-
Yokohama、日本
- Boehringer Ingelheim Investigational Site
-
Yokosuka、日本
- Boehringer Ingelheim Investigational Site
-
Yokote、日本
- Boehringer Ingelheim Investigational Site
-
Yonabarucho、日本
- Boehringer Ingelheim Investigational Site
-
Yonezawa、日本
- Boehringer Ingelheim Investigational Site
-
Yorocho、日本
- Boehringer Ingelheim Investigational Site
-
Yoshinocho、日本
- Boehringer Ingelheim Investigational Site
-
Yufu、日本
- Boehringer Ingelheim Investigational Site
-
Yurihonjou、日本
- Boehringer Ingelheim Investigational Site
-
-
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 孩子
- 成人
- 年长者
接受健康志愿者
不
有资格学习的性别
全部
取样方法
非概率样本
研究人群
COPD patients in daily clinical settings.
描述
Inclusion Criteria:
- Patients with COPD
Exclusion Criteria:
-There is no exclusion criterion, because this post marketing study (PMS) is observational survey under condition of normal clinical practice
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
队列和干预
团体/队列 |
干预/治疗 |
---|---|
慢性阻塞性肺病患者
|
Survey of patients with COPD using Spiriva (tiotropium bromide) inhalation capsules
|
研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
---|---|
Number of patients with adverse events
大体时间:Up to 4 weeks after start of treatment
|
Up to 4 weeks after start of treatment
|
Number of patients with adverse drug reactions
大体时间:Up to 4 weeks after start of treatment
|
Up to 4 weeks after start of treatment
|
Number of patients with serious adverse events
大体时间:Up to 4 weeks after start of treatment
|
Up to 4 weeks after start of treatment
|
次要结果测量
结果测量 |
大体时间 |
---|---|
Physician's overall judgement by medical interview into four grades: 1. Improved 2. No Change 3. Aggravated 4.Unassessable
大体时间:Up to 4 weeks after start of treatment
|
Up to 4 weeks after start of treatment
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始
2005年4月1日
初级完成 (实际的)
2007年9月1日
研究注册日期
首次提交
2008年1月31日
首先提交符合 QC 标准的
2014年6月26日
首次发布 (估计)
2014年6月27日
研究记录更新
最后更新发布 (估计)
2014年6月27日
上次提交的符合 QC 标准的更新
2014年6月26日
最后验证
2014年6月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.