芪苈强心胶囊对肺动脉高压的干预作用

注册号:

Registration number:

ChiCTR2500100579 

最近更新日期:

Date of Last Refreshed on:

2025-04-11 08:51:52 

注册时间:

Date of Registration:

2025-04-11 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

芪苈强心胶囊对肺动脉高压的干预作用

Public title:

The intervention effect of Qili Qiangxin Capsules on pulmonary arterial hypertension

注册题目简写:

English Acronym:

研究课题的正式科学名称:

芪苈强心胶囊对左心疾病致肺高血压的作用及机制

Scientific title:

The effect and mechanism of Qili Qiangxin Capsules on pulmonary hypertension caused by left heart disease

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:

梁明亭 

研究负责人:

梁明亭 

Applicant:

Ming-ting Liang 

Study leader:

Ming-ting Liang 

申请注册联系人电话:

Applicant telephone:

+86 178 6253 6696

研究负责人电话:

Study leader's
telephone:

+86 635 827 6837

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:

lmting007@163.com

研究负责人电子邮件:

Study leader's E-mail:

lmting007@163.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:

山东省聊城市东昌西路67号聊城市人民医院

研究负责人通讯地址:

山东省聊城市东昌西路67号

Applicant address:

No. 67 Dongchang West Road, Liaocheng People's Hospital, Shandong Province

Study leader's address:

No. 67 Dongchang West Road, Liaocheng, Shandong

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:

聊城市人民医院

Applicant's institution:

Liaocheng People's Hospital

研究负责人所在单位:

聊城市人民医院

Affiliation of the Leader:

Liaocheng People's Hospital

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:

2025022

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:

聊城市人民医院医学伦理委员会

Name of the ethic committee:

Ethics Committee of Liaocheng People's Hospital

伦理委员会批准日期:

Date of approved by ethic committee:

2025-01-14 00:00:00

伦理委员会联系人:

唐哲栋

Contact Name of the ethic committee:

Tang ZheDong

伦理委员会联系地址:

山东省聊城市东昌西路67号

Contact Address of the ethic committee:

No. 67 Dongchang West Road, Liaocheng, Shandong

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 635 827 5750

伦理委员会联系人邮箱:

Contact email of the ethic committee:

tangzhedong@sina.com

研究实施负责(组长)单位:

聊城市人民医院

Primary sponsor:

Liaocheng People's Hospital

研究实施负责(组长)单位地址:

山东省聊城市东昌西路67号

Primary sponsor's address:

No. 67 Dongchang West Road, Liaocheng, Shandong

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

山东省

市(区县):

Country:

China

Province:

Shandong

City:

单位(医院):

聊城市人民医院

具体地址:

山东省聊城市东昌西路67号

Institution
hospital:

Liaocheng People's Hospital

Address:

No. 67 Dongchang West Road, Liaocheng, Shandong

经费或物资来源:

山东第二医科大学附属医院科技发展项目

Source(s) of funding:

Science and Technology Development Project of Shandong Second Medical University Affiliated Hospital

研究疾病:

左心疾病所致的肺高血压(包括心肌病、心力衰竭、心脏瓣膜病等),主要表现为胸闷、乏力、水肿、纳差、咳嗽等症状。  

Target disease:

Pulmonary hypertension caused by left heart disease

研究疾病代码:

Target disease code:

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

上市后药物 

Study phase:

4

研究设计:

非随机对照试验 

Study design:

Non randomized control 

研究目的:

芪苈强心胶囊对左心疾病所致肺高血压的干预作用及可能机制  

Objectives of Study:

The intervention effect and possible mechanism of Qili Qiangxin Capsules on pulmonary hypertension caused by left heart disease

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

Inclusion criteria

排除标准:

1.其它分类的肺高血压类型或正在口服降肺动脉高压的靶向药物;
2.合并急性炎症反应;
3.严重肝肾功能不全;
4.合并恶性肿瘤或自身免疫性疾病;

Exclusion criteria:

1.Other types of pulmonary hypertension or targeted drugs for oral lowering of pulmonary arterial hypertension;combined with acute inflammatory response;
2.Concomitant acute inflammatory disease;
3.severe liver and kidney dysfunction;
4.Merge malignant tumors or Immunodeficiency diseases;

研究实施时间:

Study execute time:

From 2025-01-01 00:00:00 To 2027-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2025-04-16 00:00:00 To 2026-03-31 00:00:00

干预措施:

Interventions:

组别:

常规药物治疗组

样本量:

100

Group:

Conventional medication group

Sample size:

干预措施:

指南推荐治疗心力衰竭的规范药物

干预措施代码:

Intervention:

Guidelines recommend standardized drugs for the treatment of heart failure

Intervention code:

组别:

联合芪苈强心胶囊组

样本量:

100

Group:

combined Qiliqiangxin capsule group

Sample size:

干预措施:

联合芪苈强心胶囊

干预措施代码:

Intervention:

combined Qiliqiangxin capsule

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

山东 

市(区县):

 

Country:

China

Province:

Shandong

City:

单位(医院):

聊城市人民医院 

单位级别:

三级甲等 

Institution
hospital:

Liaocheng People's Hospital

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

高迁移率族蛋白B1

指标类型:

次要指标

Outcome:

HMGB1

Type:

Secondary indicator

测量时间点:

治疗前及治疗后3月、6月及12月

测量方法:

酶联免疫吸附实验

Measure time point of outcome:

Before and after treatment for 3 months, 6 months, and 12 months

Measure method:

Elisa

指标中文名:

肺动脉收缩压

指标类型:

主要指标

Outcome:

Pulmonary artery systolic pressure

Type:

Primary indicator

测量时间点:

治疗前及治疗后3月、6月及12月

测量方法:

超声心动图

Measure time point of outcome:

Before and after treatment for 3 months, 6 months, and 12 months

Measure method:

Echocardiogram

指标中文名:

乳腺和肾脏表达的趋化因子

指标类型:

次要指标

Outcome:

CXCL14

Type:

Secondary indicator

测量时间点:

治疗前及治疗后3月、6月及12月

测量方法:

酶联免疫吸附实验

Measure time point of outcome:

Before and after treatment for 3 months, 6 months, and 12 months

Measure method:

Elisa

指标中文名:

6 分钟步行试验

指标类型:

次要指标

Outcome:

6 minutes walk test

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

氨基末端B型利钠肽前体

指标类型:

次要指标

Outcome:

NT-proBNP

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

WHO 分级

指标类型:

次要指标

Outcome:

WHO classification

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:

尚未开始

Not yet 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):

由研究者根据患者的治疗依从性分组

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

Grouping by researchers based on patients' treatment compliance

是否公开试验完成后的统计结果:

Calculated Results after the Study Completed public access:

不公开/Private

盲法:

开放标签

Blinding:

Open-label study

是否共享原始数据:

IPD sharing

是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):

原始数据公开日期:2027年6月。公开方式:可通过联系研究负责人邮箱获取(lmting007@163.com)

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

You can obtain it by contacting the email of the research leader(lmting007@163.com)

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:

患者数据采集通过电子病历获得,并建立电子文档进行专人管理。

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

Patient data collection is obtained through electronic medical records, and electronic documents are established for dedicated management.

数据与安全监察委员会:

Data and Safety Monitoring Committee:

无/No

注册人:

Name of Registration:

 2025-04-11 08:51:32