A multicenter, prospective, real-world study on the treatment of stable chronic obstructive pulmonary disease with Guben Kechuan granules

注册号:

Registration number:

ITMCTR2024000226

最近更新日期:

Date of Last Refreshed on:

2024-08-13

注册时间:

Date of Registration:

2024-08-13

注册号状态:

Registration Status:

预注册

Prospective registration

注册题目:

固本咳喘颗粒治疗稳定期慢性阻塞性肺疾病多中心、前瞻性真实世界研究

Public title:

A multicenter, prospective, real-world study on the treatment of stable chronic obstructive pulmonary disease with Guben Kechuan granules

注册题目简写:

English Acronym:

研究课题的正式科学名称:

固本咳喘颗粒治疗稳定期慢性阻塞性肺疾病多中心、前瞻性真实世界研究

Scientific title:

A multicenter, prospective, real-world study on the treatment of stable chronic obstructive pulmonary disease with Guben Kechuan granules

研究课题的正式科学名称简写:

Scientific title acronym:

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:

胡明瑞

研究负责人:

张炜

Applicant:

Hu Mingrui

Study leader:

Zhang Wei

申请注册联系人电话:

Applicant telephone:

+86 187 6273 9064

研究负责人电话:

Study leader's telephone:

+86 158 2763 9709

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:

1492054276@qq.com

研究负责人电子邮件:

Study leader's E-mail:

1492054276@qq.com

申请单位网址(自愿提供):

Study leader's 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:

上海市浦东新区张衡路528号

研究负责人通讯地址:

上海市浦东新区张衡路528号

Applicant address:

528 Zhangheng Road, Pudong New Area, Shanghai

Study leader's address:

528 Zhangheng Road, Pudong New Area, Shanghai

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:

上海中医药大学附属曙光医院

Applicant's institution:

Shanghai University of Traditional Chinese Medicine Affiliated Shuguang Hospital

是否获伦理委员会批准:

Approved by ethic committee:

伦理委员会批件文号:

Approved No. of ethic committee:

2023-1359-126-01

伦理委员会批件附件:

Approved file of Ethical Committee:

View

批准本研究的伦理委员会名称:

上海中医药大学附属曙光医院伦理委员会

Name of the ethic committee:

Ethics Committee of Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine

伦理委员会批准日期:

Date of approved by ethic committee:

2023/9/27 0:00:00

伦理委员会联系人:

马俊坚

Contact Name of the ethic committee:

Ma Junjian

伦理委员会联系地址:

上海市浦东新区张衡路528号

Contact Address of the ethic committee:

528 Zhangheng Road, Pudong New Area, Shanghai

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 21 2025 6070

伦理委员会联系人邮箱:

Contact email of the ethic committee:

1492054276@qq.com

研究实施负责(组长)单位:

上海中医药大学附属曙光医院

Primary sponsor:

Shanghai University of Traditional Chinese Medicine Affiliated Shuguang Hospital

研究实施负责(组长)单位地址:

上海市浦东新区张衡路528号

Primary sponsor's address:

528 Zhangheng Road, Pudong New Area, Shanghai

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

上海

市(区县):

Country:

China

Province:

Shanghai

City:

单位(医院):

上海中医药大学附属曙光医院

具体地址:

上海市浦东新区张衡路528号

Institution
hospital:

Shanghai University of Traditional Chinese Medicine Affiliated Shuguang Hospital

Address:

528 Zhangheng Road, Pudong New Area, Shanghai

经费或物资来源:

自筹

Source(s) of funding:

self-funded

研究疾病:

慢性阻塞性肺疾病

研究疾病代码:

Target disease:

chronic obstructive pulmonary disease

Target disease code:

研究类型:

Study type:

干预性研究

Interventional study

研究设计:

Study design:

随机平行对照

randomized controlled trial(parallel group design)

研究所处阶段:

Study phase:

上市后药物

Post-marketing clinical trial

研究目的:

1.评价在真实医疗环境下,固本咳喘颗粒治疗稳定期慢性阻塞性肺疾病患者的临床转归; 2.评估固本咳喘颗粒在慢性阻塞性肺疾病临床应用的安全性。

Objectives of Study:

1. To evaluate the clinical outcomes of Guben Kechuan Granules in treating stable chronic obstructive pulmonary disease patients in a real medical environment; 2. To evaluate the safety of Guben Kechuan Granules in clinical application of chronic obstructive pulmonary 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:

1.符合慢性阻塞性肺疾病西医诊断标准; 2.符合慢性阻塞性肺疾病中医“肺肾两虚”证候诊断标准; 3.慢性阻塞性肺疾病临床稳定期,近4周无呼吸道感染及AECOPD; 4.年龄18-80岁,性别不限; 5.自愿接受治疗,并签署知情同意书。

Inclusion criteria

1. Meets the diagnostic criteria of Western medicine for chronic obstructive pulmonary disease; 2. Meets the diagnostic criteria for the "lung kidney deficiency" syndrome of chronic obstructive pulmonary disease in traditional Chinese medicine; 3. Chronic obstructive pulmonary disease is clinically stable, with no respiratory infections or AECOPD in the past 4 weeks; 4. Aged 18-80 years old, regardless of gender; 5. Volunteer to receive treatment and sign an informed consent form.

排除标准:

1.哮喘、支气管扩张、肺纤维化所致的气流受限患者; 2.曾接受肺移植术或肺切除术者; 3.患有严重的高血压、心力衰竭、心律失常、糖尿病、原发性心、肝、肾、血液、神经系统症状等控制不理想者; 4.肺部肿瘤、恶性肿瘤(距离初次诊断时间<5年,或存在影像学或肿瘤标记物等检查证实的复发、转移,或正在进行放疗、化疗、靶向治疗、免疫治疗等); 5.对已知药物成分过敏者; 6.孕妇、计划妊娠或哺乳期妇女; 7.研究者认为不适合入组者。

Exclusion criteria:

1. Patients with airflow restriction caused by asthma, bronchiectasis, and pulmonary fibrosis; 2. Those who have undergone lung transplantation or pneumonectomy; 3. Patients with severe hypertension, heart failure, arrhythmia, diabetes, primary heart, liver, kidney, blood, nervous system symptoms and other poor control; 4. Lung tumors, malignant tumors (less than 5 years from initial diagnosis, or with recurrence or metastasis confirmed by imaging or tumor markers, or undergoing radiotherapy, chemotherapy, targeted therapy, immunotherapy, etc.); 5. Individuals who are allergic to known drug ingredients; 6. Pregnant, planned or lactating women; 7. Researchers believe that it is not suitable for inclusion in the study.

研究实施时间:

Study execute time:

From 2024-09-01

To      2027-08-31

征募观察对象时间:

Recruiting time:

From 2024-09-01

To      2027-08-31

干预措施:

Interventions:

组别:

观察者

样本量:

150

Group:

Observation Group

Sample size:

干预措施:

常规治疗+固本咳喘颗粒

干预措施代码:

Intervention:

Routine treatment+Guben Kechuan granules

Intervention code:

组别:

对照组

样本量:

50

Group:

Control Group

Sample size:

干预措施:

常规治疗

干预措施代码:

Intervention:

Routine treatmen

Intervention code:

样本总量 Total sample size : 200

研究实施地点:

Countries of recruitment
and research settings:

国家:

中国

省(直辖市):

上海

市(区县):

Country:

China

Province:

Shanghai

City:

单位(医院):

上海中医药大学附属曙光医院

单位级别:

三级甲等

Institution/hospital:

Shanghai University of Traditional Chinese Medicine Affiliated Shuguang Hospital

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

慢阻肺急性加重(AECOPD)在观察期的发生频率

指标类型:

主要指标

Outcome:

The frequency of acute exacerbation of chronic obstructive pulmonary disease (AECOPD) during the observation period

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

首次AECOPD发作严重程度

指标类型:

次要指标

Outcome:

Severity of first AECOPD attack

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

观察期内中/重度AECOPD发生频率

指标类型:

次要指标

Outcome:

Frequency of moderate/severe AECOPD during the observation period

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

中医症候积分

指标类型:

次要指标

Outcome:

Traditional Chinese Medicine Syndrome Score

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

匹兹堡睡眠质量指数量表

指标类型:

附加指标

Outcome:

Pittsburgh Sleep Quality Index Scale

Type:

Additional indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

临床重要恶化指标(CID)

指标类型:

次要指标

Outcome:

Clinical Significant Deterioration Indicators (CID)

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

焦虑自评量表

指标类型:

附加指标

Outcome:

Self-rating anxiety scale

Type:

Additional indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

6分钟步行距离

指标类型:

次要指标

Outcome:

6-minute walking distance

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

呼吸困难评分分级

指标类型:

次要指标

Outcome:

Respiratory difficulty score grading

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

健康状况调查问卷

指标类型:

附加指标

Outcome:

Health Survey Questionnaire

Type:

Additional 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

指标类型:

次要指标

Outcome:

Lung function indicators

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

SpO2

指标类型:

附加指标

Outcome:

SpO2

Type:

Additional indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

自我评估测试

指标类型:

次要指标

Outcome:

Self Assessment 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:

主要临床症状评分

指标类型:

次要指标

Outcome:

Main clinical symptom score

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:

尚未开始

Not yet recruiting

年龄范围:

最小 18
Min age years
最大 80
Max age years

Recruiting status:

Participant age:

性别:

Gender:

男女均可

Both

随机方法(请说明由何人用什么方法产生随机序列):

随机方式:实效性随机。 随机原则:遵循患者意愿,同意随机的患者按简单随机法入组;不愿随机的,按患者意愿入组。

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

Random method: Effectiveness random. Randomization principle: Following the patient's wishes, patients who agree to be randomized will be enrolled using a simple randomization method; Those who do not wish to be randomized will be enrolled according to the patient's wishes.

盲法:

Blinding:

NA

是否共享原始数据:

IPD sharing:

No

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):

COPD专病库 http://copd.shivictory.com/home/main

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

COPD specialized disease library http://yun.shivictory.com/home/main/

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:

COPD专病库 http://copd.shivictory.com/home/main

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

COPD specialized disease library http://yun.shivictory.com/home/main/

数据管理委员会:

Data Managemen Committee:

Yes

研究计划书或研究结果报告发表信息
(杂志名称、期、卷、页,时间;或网址):

Publication information of the protocol/research results report
(name of the journal, volume, issue, pages, time; or website):

ITMCTR BJ-ICP:07032215-5 Tip: IE8 is recommended Use the system with widescreen display resolution above