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注册号: Registration number: |
ChiCTR-TRC-09000460 |
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最近更新日期: Date of Last Refreshed on: |
2015-05-15 12:52:16 |
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注册时间: Date of Registration: |
2009-07-20 00:00:00 |
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注册号状态: |
补注册 |
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Registration Status: |
Retrospective registration |
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注册题目: |
大剂量N-乙酰半胱氨酸对治疗中、重度慢性阻塞性肺病病情加重的有效性和安全性的双盲安慰剂对照研究 |
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Public title: |
Placebo-controlled study on efficacy and safety of N-acetylysteine high dose in exacerbation of chronic obstructive plumonary disease |
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注册题目简写: |
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English Acronym: |
PANTHEON STUDY |
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研究课题的正式科学名称: |
大剂量N-乙酰半胱氨酸对治疗中、重度慢性阻塞性肺病病情加重的有效性和安全性的双盲安慰剂对照研究 |
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Scientific title: |
Placebo-controlled study on efficacy and safety of N-acetylysteine high dose in exacerbation of chronic obstructive plumonary disease |
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研究课题代号(代码): Study subject ID: |
4999M01 |
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在二级注册机构或其它机构的注册号: The registration number of the Partner Registry or other register: |
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申请注册联系人: |
夏其奎 |
研究负责人: |
钟南山 |
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Applicant: |
Qikui Xia |
Study leader: |
Nanshan Zhong |
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申请注册联系人电话: Applicant telephone: |
+86 13910737494 |
研究负责人电话:
Study leader's |
+86 020 83337750-6062 |
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申请注册联系人传真 : Applicant Fax: |
+86 010 87766547 |
研究负责人传真: Study leader's fax: |
+86 020 83186583 |
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申请注册联系人电子邮件: Applicant E-mail: |
xiaqikui@zambon.com.cn |
研究负责人电子邮件: Study leader's E-mail: |
xiaqikui@zambon.com.cn |
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申请单位网址(自愿提供): Applicant website(voluntary supply): |
http://www.zambon.com.cn/ |
研究负责人网址(自愿提供): Study leader's website(voluntary supply): |
http://www.gird.cn/ |
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申请注册联系人通讯地址: |
北京市西城区展览馆路外交学院24号院3号楼3单元201号 |
研究负责人通讯地址: |
广州市沿江西路151号广州医学院第一附属医院广州呼吸疾病研究所 |
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Applicant address: |
Room201, Tower 3, Unit 3, No.24, Zhanlanguan Road,Xicheng District, Beijing, China |
Study leader's address: |
No.151, West Yanjiang Road, Guangzhou City |
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申请注册联系人邮政编码: Applicant postcode: |
100037 |
研究负责人邮政编码: Study leader's postcode: |
510120 |
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申请人所在单位: |
海南赞邦制药有限公司 |
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Applicant's institution: |
Hainan Zambon Pharmaceuitical CO., Ltd |
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研究负责人所在单位: |
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Affiliation of the Leader: |
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是否获伦理委员会批准: |
是 |
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Approved by ethic committee: |
Yes |
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伦理委员会批件文号: Approved No. of ethic committee: |
医伦审(2009)第05号 |
伦理委员会批件附件: Approved file of Ethical Committee: |
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批准本研究的伦理委员会名称: |
广州医学院第一附属医院广州呼吸疾病研究所 |
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Name of the ethic committee: |
Ethics Commiitte of the First Affiliated Hospital of Guangzhou Medical College |
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伦理委员会批准日期: Date of approved by ethic committee: |
2013-08-26 00:00:00 | ||
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伦理委员会联系人: |
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Contact Name of the ethic committee: |
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伦理委员会联系地址: |
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Contact Address of the ethic committee: |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
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研究实施负责(组长)单位: |
广州医学院第一附属医院 |
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Primary sponsor: |
First Affiliated Hospital of Guangzhou Medical College |
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研究实施负责(组长)单位地址: |
广州市沿江西路151号广州医学院第一附属医院广州呼吸疾病研究所 |
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Primary sponsor's address: |
No.151, West Yanjiang Road, Guangzhou City |
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试验主办单位(项目批准或申办者): Secondary sponsor: |
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经费或物资来源: |
海南赞邦公司提供 |
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Source(s) of funding: |
Hainan Zambon Pharmaceuitical CO., Ltd |
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研究疾病: |
慢性阻塞性肺病(COPD) |
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Target disease: |
Chronic Obstructive Pulmonary Disease |
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研究疾病代码: |
L07 |
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Target disease code: |
L07 |
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研究类型: |
干预性研究 |
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Study type: |
Interventional study |
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研究所处阶段: |
上市后药物 | ||||||||||||||||||||||
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Study phase: |
4 |
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研究设计: |
随机平行对照 |
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Study design: |
Parallel |
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研究目的: |
本研究旨在研究每天富露施1200mg在降低中度到重度慢性阻塞性肺病(COPD)的患者的急性加重率的有效性 |
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Objectives of Study: |
To investigate the efficacy of N-acetylcysteine 1200 mg (600 twice a day) in reducing the exacerbation rate in patients suffering from moderate to severe Chronic Obstructive Pulmonary Disease (COPD). |
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药物成份或治疗方案详述: |
乙酰半胱氨酸片 活性成分:乙酰半胱氨酸 600mg 安慰剂 活性成份:0 |
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Description for medicine or protocol of treatment in detail: |
NAC activities components: NAC 600mg Placebo active components: Acetylcysteine 0mg |
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纳入标准: |
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Inclusion criteria |
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排除标准: |
? 诊断患有支气管哮喘, 囊肿性纤维化, 活动性肺结核, 肺炎, 支气管肺炎, 支气管扩张, 肺癌或者肺转移癌, 其它进展性致命疾病的患者。 |
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Exclusion criteria: |
1. Patients with a diagnosis of bronchial asthma, cystic fibrosis, active pulmonary tuberculosis, pneumonia, bronchial pneumonia, bronchiectasis, lung cancer or lung metastases, other progressively fatal disease; |
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研究实施时间: Study execute time: |
从 From 2009-02-01 00:00:00至 To 1990-01-01 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2009-06-01 00:00:00 至 To 2010-02-28 00:00:00 |
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干预措施: Interventions: |
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研究实施地点: Countries of recruitment and research settings: |
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测量指标: Outcomes: |
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采集人体标本:
Collecting sample(s)
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征募研究对象情况: Recruiting status: |
结束 /Completed |
年龄范围: Participant age: |
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性别: |
男女均可 |
Gender: |
Both |
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随机方法(请说明由何人用什么方法产生随机序列): |
计算机软件 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Computer Software |
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是否公开试验完成后的统计结果: Calculated Results after the Study Completed public access: |
公开/Public |
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盲法: |
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Blinding: |
Statistician: Blinding Investigator: Blinding Subjects: Blinding |
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试验完成后的统计结果(上传文件): |
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Calculated Results after
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是否共享原始数据: IPD sharing |
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共享原始数据的方式(说明:请填入公开原始数据日期和方式,如采用网络平台,需填该网络平台名称和网址): |
上海杰诚医药科技有限公司 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Medkey Med-Tech Development Co.,Ltd |
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数据采集和管理(说明:数据采集和管理由两部分组成,一为病例记录表(Case Record Form, CRF),二为电子采集和管理系统(Electronic Data Capture, EDC),如ResMan即为一种基于互联网的EDC: |
上海杰诚医药科技有限公司 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Medkey Med-Tech Development Co.,Ltd |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |