ChiCTR2000035406 版本V1.0 版本创建时间2020/08/10 22:59:53 中国临床试验注册中心

审核状态:

Project audit state:

通过审核

Successful

注册号:

Registration number:

ChiCTR2000035406 

最近更新日期:

Date of Last Refreshed on:

2020-08-10 22:59:47 

注册时间:

Date of Registration:

1990-01-01 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

审核中(一)磺达肝癸钠用于预防呼吸系统疾病患者静脉血栓栓塞事件:多中心、前瞻性、随机、对照研究

Public title:

Fondaparinux in the prevention of venous thromboembolism in patients with respiratory diseases: a multicenter, prospective, randomized, controlled trial

注册题目简写:

Foster

English Acronym:

Foster

研究课题的正式科学名称:

磺达肝癸钠用于预防呼吸系统疾病患者静脉血栓栓塞事件:多中心、前瞻性、随机、对照研究

Scientific title:

Fondaparinux in the prevention of venous thromboembolism in patients with respiratory diseases: a multicenter, prospective, randomized, controlled trial

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:

曹洁 

研究负责人:

曹洁 

Applicant:

JieCao 

Study leader:

JieCao 

申请注册联系人电话:

Applicant telephone:

13132088076

研究负责人电话:

Study leader's telephone:

13132088076

申请注册联系人传真 :

Applicant Fax:

研究负责人传真:

Study leader's fax:

申请注册联系人电子邮件:

Applicant E-mail:

tjcaojie@sina.com

研究负责人电子邮件:

Study leader's E-mail:

tjcaojie@sina.com

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:

天津市和平区鞍山道154号天津医科大学总医院

研究负责人通讯地址:

天津市和平区鞍山道154号天津医科大学总医院

Applicant address:

General Hospital of Tianjin Medical University, 154 Anshan Road, Heping District, Tianjin

Study leader's address:

General Hospital of Tianjin Medical University, 154 Anshan Road, Heping District, Tianjin

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:

天津医科大学总医院

Applicant's institution:

Tianjin Medical University 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:

是/Yes

Approved by ethic committee:

Yes

伦理委员会批件文号:

Approved No. of ethic committee:

IRB2020-YX-03301

伦理委员会批件附件:

Approved file of Ethical Committee:

查看附件View

批准本研究的伦理委员会名称:

天津医科大学总医院医学伦理委员会

Name of the ethic committee:

Medical ethics committee of General Hospital of Tianjin Medical University

伦理委员会批准日期:

Date of approved by ethic committee:

2020-07-02 00:00:00

伦理委员会联系人:

金冬来

Contact Name of the ethic committee:

Donglai Jin

伦理委员会联系地址:

天津市和平区鞍山道154号天津医科大学总医院科研楼1楼伦理委员会办公室

Contact Address of the ethic committee:

Ethics committee office, 1st floor, scientific research building, Tianjin Medical University General Hospital, 154 Anshan Road, Heping District, Tianjin

伦理委员会联系人电话:

Contact phone of the ethic committee:

0226.361044

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:

天津医科大学总医院

Primary sponsor:

Tianjin Medical University General Hospital

研究实施负责(组长)单位地址:

天津市和平区鞍山道154号天津医科大学总医院

Primary sponsor's address:

General Hospital of Tianjin Medical University, 154 Anshan Road, Heping District, Tianjin

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

天津

市(区县):

和平区

Country:

China

Province:

Tianjin

City:

Heping District

单位(医院):

天津医科大学总医院

具体地址:

和平区鞍山道154号

Institution
hospital:

Tianjin Medical University General Hospital

Address:

154 Anshan Road, Heping District

经费或物资来源:

中国健康促进基金会

Source(s) of funding:

China Health Promotion Foundation

Target disease:

Chronic obstructive pulmonary disease (COPD), lung cancer, interstitial lung disease, pneumonia

Target disease code:

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

探索性研究/预试验 

Study phase:

0

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

主要研究目的:评价两种抗凝药物磺达肝癸钠和低分子肝素在预防呼吸系统疾病VTE高危风险患者中的有效性。 次要目的:评价两种抗凝药物磺达肝癸钠和低分子肝素在预防呼吸系统疾病VTE高危风险患者中的安全性。  

Objectives of Study:

Objective: To evaluate the efficacy of two anticoagulant drugs fondaparinux and low molecular weight heparin in the prevention of respiratory diseases with high risk of VTE. Secondary objective: To evaluate the safety of two anticoagulants fondaparinux sodium and low molecular weight heparin in the prevention of respiratory diseases in patients at high risk of VTE.

药物成份或治疗方案详述:

磺达肝癸钠组:2.5mg,QD,皮下注射,7-14天给药; 低分子肝素组:4000 AxaIU (0.4 ml),皮下注射,QD,7-14天给药 

Description for medicine or protocol of treatment in detail:

Fondaparinux sodium group: 2.5mg QD, subcutaneous injection, 7-14 days; Low molecular weight heparin group: 4000 axaiu (0.4 ml), subcutaneous injection, QD, 7-14 days 

纳入标准:

1.年龄≥18岁的呼吸系统疾病住院患者;
2.根据Padua评分≥4分,需要使用抗凝药物进行VTE预防的患者;
3.患者或法定代理人已被告知研究的性质,理解方案中的规定,能够保证依从性;

Inclusion criteria

1. Hospitalized patients with respiratory diseases over 18 years old;

2. Patients who need anticoagulant drugs to prevent VTE according to Padua score ≥ 4;

3. Patients or legal representatives have been informed of the nature of the study and understand the provisions in the protocol to ensure compliance;

排除标准:

1.对磺达肝癸钠和依诺肝素过敏或存在禁忌症;
2.出血高风险:出血性疾病、出血倾向、出血体质或凝血障碍患者或病史;
3.存在甲状腺功能亢进、严重肝肾功能不全等抗凝药物使用禁忌患者;
4.已参与其他药物/器械的研究或在另一药物/器械研究的随访期间;
5.患者可能对研究方案不依从(包括随访期),如精神异常、酗酒或吸毒等;

Exclusion criteria:

1. Allergy or contraindication to fondaparinux and enoxaparin;

2. High risk of bleeding: patients or history of hemorrhagic diseases, bleeding tendency, bleeding constitution or coagulation disorders;

3. Patients with hyperthyroidism and severe hepatic and renal insufficiency were contraindicated;

4. Having participated in the research of other drugs / devices or during the follow-up period of another drug / device research;

5. Patients may not comply with the research protocol (including the follow-up period), such as mental disorders, alcohol or drug abuse, etc;

研究实施时间:

Study execute time:

From 2020-07-31 00:00:00 To 2020-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2020-07-31 00:00:00 To 2021-01-31 00:00:00  

干预措施:

Interventions:

组别:

磺达肝癸钠

样本量:

564

Group:

Fondaparinux sodium

Sample size:

干预措施:

2.5mg,QD,皮下注射,7-14天给药;

干预措施代码:

Intervention:

5 mg, QD, subcutaneous injection, 7-14 days.

Intervention code:

组别:

低分子肝素

样本量:

564

Group:

Low molecular weight heparin

Sample size:

干预措施:

4000 AxaIU (0.4 ml),QD,皮下注射,7-14天给药

干预措施代码:

Intervention:

4000 axaiu (0.4 ml), QD, subcutaneous injection, 7-14 days

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

天津 

市(区县):

和平区 

Country:

China 

Province:

Tianjin 

City:

Heping District 

单位(医院):

天津医科大学总医院 

单位级别:

三甲 

Institution
hospital:

Tianjin Medical University General Hospital

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

7天血栓事件(包括下肢深静脉血栓形成,肺栓塞,导管内血栓形成)

指标类型:

主要指标

Outcome:

7-day thrombotic events (including lower extremity deep vein thrombosis, pulmonary embolism, and intraductal thrombosis)

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

7天出血事件(任何出血事件,血小板减少)

指标类型:

主要指标

Outcome:

7-day bleeding event (any bleeding event, thrombocytopenia)

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

30天出血事件

指标类型:

次要指标

Outcome:

30 day bleeding events

Type:

Secondary 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:

标本中文名:

血液

组织:

Sample Name:

blood

Tissue:

人体标本去向

使用后销毁  

说明

Fate of sample:

Destruction after use  

Note:

征募研究对象情况:

Recruiting status:

正在进行

Recruiting

年龄范围:

Participant age:

最小 Min age 18 years
最大 Max age 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):

由研究医生使用电子数据收集系统(EDC)对患者进行1:1随机分配

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

Patients were randomly assigned by the study doctor using the electronic data collection system (EDC)

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:

本研究采用开放设计。

Blinding:

This study adopts open design.

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

Yes

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):

试验文章发表以论文的形式

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

Experimental articles are published in the form of papers

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:

填写病历报告表,使用电子采集和管理系统进行数据管理

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

Fill in the medical record report form, and use the electronic collection and management system for data management

数据与安全监察委员会:

Data and Safety Monitoring Committee:

暂未确定/Not yet

注册人:

Name of Registration:

 2020-08-10 22:59:47