阻塞性睡眠呼吸中止症對慢性阻塞性肺病病人 (重疊症候群)之影響:就缺氧與心血管事件之生物標記之研究

注册号:

Registration number:

ChiCTR-OOC-15006691 

最近更新日期:

Date of Last Refreshed on:

2015-07-04 10:10:58 

注册时间:

Date of Registration:

2015-07-02 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

阻塞性睡眠呼吸中止症對慢性阻塞性肺病病人 (重疊症候群)之影響:就缺氧與心血管事件之生物標記之研究

Public title:

The impact of obstructive sleep apnea in patients with chronic obstructive pulmonary disease: Biomarkers of hypoxemia and cardiovascular events

注册题目简写:

English Acronym:

研究课题的正式科学名称:

阻塞性睡眠呼吸中止症對慢性阻塞性肺病病人 (重疊症候群)之影響:就缺氧與心血管事件之生物標記之研究

Scientific title:

The impact of obstructive sleep apnea in patients with chronic obstructive pulmonary disease: Biomarkers of hypoxemia and cardiovascular events

研究课题代号(代码):

Study subject ID:

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:

申请注册联系人:

蘇剛正 

研究负责人:

蘇剛正 

Applicant:

Kang-Cheng Su 

Study leader:

Kang-Cheng Su 

申请注册联系人电话:

Applicant telephone:

+886-2-28712121 ext 8928

研究负责人电话:

Study leader's
telephone:

+886-2-28712121 ext 8928

申请注册联系人传真 :

Applicant Fax:

+886-2-77368928

研究负责人传真:

Study leader's fax:

+886-2-77368928

申请注册联系人电子邮件:

Applicant E-mail:

kcsu@vghtpe.gov.tw

研究负责人电子邮件:

Study leader's E-mail:

kcsu@vghtpe.gov.tw

申请单位网址(自愿提供):

Applicant website(voluntary supply):

研究负责人网址(自愿提供):

Study leader's website(voluntary supply):

申请注册联系人通讯地址:

台灣臺北市北投區石牌路二段 201 號

研究负责人通讯地址:

台灣臺北市北投區石牌路二段 201 號

Applicant address:

No.201, Sec. 2, Shipai Rd., Beitou District, Taipei City, Taiwan 11217

Study leader's address:

No.201, Sec. 2, Shipai Rd., Beitou District, Taipei City, Taiwan 11217

申请注册联系人邮政编码:

Applicant postcode:

研究负责人邮政编码:

Study leader's postcode:

申请人所在单位:

臺北榮民總醫院

Applicant's institution:

Taipei Veterans General Hospital

研究负责人所在单位:

Affiliation of the Leader:

是否获伦理委员会批准:

Approved by ethic committee:

Yes

伦理委员会批件文号:

Approved No. of ethic committee:

2015-04-008BC

伦理委员会批件附件:

Approved file of Ethical Committee:

批准本研究的伦理委员会名称:

臺北榮民總醫院人體試驗委員會

Name of the ethic committee:

Institutinal Review Board of Taipei Veterans General Hospital

伦理委员会批准日期:

Date of approved by ethic committee:

2015-04-14 00:00:00

伦理委员会联系人:

Contact Name of the ethic committee:

伦理委员会联系地址:

Contact Address of the ethic committee:

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:

研究实施负责(组长)单位:

Department of Chest Medicine

Primary sponsor:

Yen Tjing Ling Medical Foundtion

研究实施负责(组长)单位地址:

台灣臺北市北投區石牌路二段 201 號

Primary sponsor's address:

No.201, Sec. 2, Shipai Rd., Beitou District, Taipei City, Taiwan 11217

试验主办单位(项目批准或申办者):

Secondary sponsor:

经费或物资来源:

嚴慶齡基金會

Source(s) of funding:

Yen Tjing Ling Medical Foundtion

研究疾病:

阻塞性睡眠呼吸中止症, 慢性阻塞性肺病  

Target disease:

obstructive sleep apnea, COPD

研究疾病代码:

Target disease code:

研究类型:

观察性研究

Study type:

Observational study

研究所处阶段:

其它 

Study phase:

N/A

研究设计:

单臂 

Study design:

Single arm 

研究目的:

比較不同疾病類型之以下指標 (慢性阻塞性肺病 阻塞性睡眠呼吸中止症 重疊症候群): a.血中生物標記:HIF-1, IL-6, CRP, fibrinogen, D-dimer, NT-pro-BNP。 b.臨床指標:肺功能(FEV1、FVC),睡眠檢查參數(AHI、desaturation time)  

Objectives of Study:

To compare patients categoried by differest group (COPD, OSA, overlap) 1. The difference of serum biomarkers represented by serum HIF-1, IL-6, CRP, fibrinogen, D-dimer, NT-pro-BNP among the three groups; 2. The association of inflammation markers and PSG data ( including AHI, desaturation time), and clinical data (including lung function, BMI, cardiac echo).

药物成份或治疗方案详述:

無藥物介入 

Description for medicine or protocol of treatment in detail:

No drug intervention 

纳入标准:

Inclusion criteria

排除标准:

a. 合併明顯支氣管擴張症、肺癌、活動性肺結核或其他肺部 疾病足以影響研究結果者。
b. 懷疑惑已證實有血栓性疾病者(如心肌梗塞、腦血管栓塞、深層靜脈栓塞、或肺栓塞等)。
c. 病人已有顯著之心血管問題者(缺血性心臟病、瓣膜性心臟病、心肌病變、主動脈瘤、心衰竭等)。
d. 過去4週有使用過抗生素或全身性類固醇者。

Exclusion criteria:

1. Clinically overt bronchiectasis, lung cancer, active tuberculosis, or other known specific pulmonary disease and a chest X-ray indicating diagnosis other than COPD that might interfere with the study;
2. Suspected or proven thromboemolic diseases, such as cerebral or myocardial infaction, pulmonary embolism, deep vein thrombosis, etc.;
3. Patients with significant cardiovascular disease (ischemic heart disease, vascular heart disease, cardiomyopathy, aortic aneurysm, heart failure);
4. Patients received systemic steroid 4 weeks prior to the commencement of study.

研究实施时间:

Study execute time:

From 2015-07-06 00:00:00 To 2017-06-30 00:00:00  

征募观察对象时间:

Recruiting time:

From 2015-07-06 00:00:00 To 2017-06-30 00:00:00

干预措施:

Interventions:

组别:

Case series

样本量:

100

Group:

Case series

Sample size:

干预措施:

Nil

干预措施代码:

Intervention:

Nil

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中國

省(直辖市):

台灣 

市(区县):

臺北市 

Country:

China

Province:

Taiwan

City:

Taibei

单位(医院):

臺北榮民總醫院 

单位级别:

臺北榮民總醫院 

Institution
hospital:

Taipei Veterans General Hospital

Level of the institution:

Taipei Veterans General Hospital

测量指标:

Outcomes:

指标中文名:

缺氧誘發因子1

指标类型:

主要指标

Outcome:

HIF-1

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

介白質-6

指标类型:

主要指标

Outcome:

IL-6

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

快速反應蛋白

指标类型:

主要指标

Outcome:

C-reactive protein

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

凝血酶原

指标类型:

主要指标

Outcome:

Fibrinogen

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

D-二聚體

指标类型:

主要指标

Outcome:

D-dimer

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

N端前腦利鈉肽

指标类型:

主要指标

Outcome:

NT-pro-BNP

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

肺功能

指标类型:

主要指标

Outcome:

lung function

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

間歇性缺氧指標

指标类型:

主要指标

Outcome:

Apnea-Hyponea-index

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

采集人体标本:

Collecting sample(s)
from participants:

征募研究对象情况:

Recruiting status:

尚未开始

Not yet recruiting

年龄范围:

Participant age:

最小 Min age 40 years
最大 Max age 90 years

性别:

男女均可

Gender:

Both

随机方法(请说明由何人用什么方法产生随机序列):

無隨機分配

Randomization Procedure (please state who generates the random number sequence and by what method):

Non-randomized study

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

盲法:

Blinding:

试验完成后的统计结果(上传文件):

Calculated Results after
the Study Completed(upload file):

是否共享原始数据:

IPD sharing

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):

臺北榮民總醫院

The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url):

Taipei Veterans General Hopspital

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:

臺北榮民總醫院

Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture:

Taipei Veterans General Hopspital

数据与安全监察委员会:

Data and Safety Monitoring Committee:

注册人:

Name of Registration:

 2015-07-04 10:10:59