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审核状态: Project audit state: |
通过审核 Successful |
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注册号: Registration number: |
ChiCTR2200057025 |
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最近更新日期: Date of Last Refreshed on: |
2023-02-03 17:50:19 |
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注册时间: Date of Registration: |
2022-02-26 00:00:00 |
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注册号状态: |
预注册 |
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Registration Status: |
Prospective registration |
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注册题目: |
肃肺平喘方改善支气管扩张症合并气流受限的临床研究 |
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Public title: |
Clinical study on improving bronchiectasis with airflow limitation by Sufei Pingchuan Decoction |
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注册题目简写: |
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English Acronym: |
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研究课题的正式科学名称: |
肃肺平喘方改善支气管扩张症合并气流受限的临床研究 |
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Scientific title: |
Clinical study on improving bronchiectasis with airflow limitation by Sufei Pingchuan Decoction |
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研究课题代号(代码): Study subject ID: |
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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: |
ChiMCTR2200005661 |
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申请注册联系人: |
袁沙沙 |
研究负责人: |
苗青 |
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Applicant: |
Yuan Shasha |
Study leader: |
Miao Qing |
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申请注册联系人电话: Applicant telephone: |
+86 18301103200 |
研究负责人电话:
Study leader's |
+86 13910812309 |
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申请注册联系人传真 : Applicant Fax: |
研究负责人传真: Study leader's fax: |
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申请注册联系人电子邮件: Applicant E-mail: |
384482587@qq.com |
研究负责人电子邮件: Study leader's E-mail: |
miaoqing55@sina.com |
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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): |
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申请注册联系人通讯地址: |
北京市海淀区西苑操场1号 |
研究负责人通讯地址: |
北京市海淀区西苑操场1号 |
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Applicant address: |
1 Xiyuan Playground, Haidian District, Beijing |
Study leader's address: |
1 Xiyuan Playground, Haidian District, Beijing |
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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: |
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申请人所在单位: |
中国中医科学院西苑医院 |
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Applicant's institution: |
Xiyuan Hospital, Chinese Academy of Chinese Medical Sciences |
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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: |
2021XLA122-4 |
伦理委员会批件附件: Approved file of Ethical Committee: |
查看附件View |
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批准本研究的伦理委员会名称: |
中国中医科学院西苑医院医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee of Xiyuan Hospital, Chinese Academy of Chinese Medical Sciences |
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伦理委员会批准日期: Date of approved by ethic committee: |
2022-01-27 00:00:00 | ||
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伦理委员会联系人: |
訾明杰 |
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Contact Name of the ethic committee: |
Zi Mingjie |
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伦理委员会联系地址: |
北京市海淀区西苑操场1号 |
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Contact Address of the ethic committee: |
1 Xiyuan Playground, Haidian District, Beijing |
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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: |
中国中医科学院西苑医院 |
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Primary sponsor: |
Xiyuan Hospital, Chinese Academy of Chinese Medical Sciences |
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研究实施负责(组长)单位地址: |
北京市海淀区西苑操场1号 |
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Primary sponsor's address: |
1 Xiyuan Playground, Haidian District, Beijing |
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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: |
中国中医科学院西苑医院 |
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Source(s) of funding: |
Xiyuan Hospital, Chinese Academy of Chinese Medical Sciences |
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研究疾病: |
支气管扩张症 |
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Target disease: |
Bronchiectasis |
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研究疾病代码: |
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Target disease code: |
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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: |
探索性研究/预试验 | ||||||||||||||||||||||
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Study phase: |
0 |
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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: |
1.探讨肃肺平喘方通过改善支气管扩张症合并气流受限,进而改善患者肺功能及生活质量的有效性;为提高支气管扩张症临床疗效提供新的理论和突破点; 2.探讨肃肺平喘方降低炎症水平,从而改善支气管扩张症合并气流受限的机制。 |
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Objectives of Study: |
1. To investigate the effectiveness of Sufei Pingchuan Decoction in improving lung function and quality of life of patients by improving bronchiectasis with airflow limitation ; to provide new theories and breakthroughs for improving the clinical efficacy of bronchiectasis ; 2.To investigate the mechanism of Sufei Pingchuan Decoction in reducing inflammation and improving bronchiectasis with airflow limitation. |
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药物成份或治疗方案详述: |
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Description for medicine or protocol of treatment in detail: |
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纳入标准: |
(1)符合支气管扩张症诊断标准的门诊病人;(2)入组前3月内肺功能显示气流受限,且经病史采集及体格检查未发现急性加重者;(3)年龄18-70岁;(4)中医辨证为肺脾气虚、痰热蕴肺者;(5)愿依从医师的诊断、治疗安排并签署知情同意书者。 |
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Inclusion criteria |
( 1 ) Outpatients who meet the diagnostic criteria of bronchiectasis ; ( 2 ) Patients whose pulmonary function showed airflow limitation within 3 months before admission, and no acute exacerbation was found by medical history collection and physical examination ; ( 3 ) 18-70 years of age ; ( 4 ) TCM syndrome differentiation for lung and spleen qi deficiency, phlegm heat lung ; ( 5 ) Wish to comply with the physician 's diagnosis, treatment arrangements and sign an informed consent. |
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排除标准: |
(1)以咯血为主要表现的干性支扩患者;(2)入组前4周内曾出现病情变化者;(3)非结核分枝杆菌(NTM)、变应性支气管肺曲霉菌病(ABPA)等特殊的支扩患者;(4)对噻托溴铵过敏者或具有药物禁忌症(如窄角型青光眼、表现严重的前列腺增生、膀胱颈狭窄及尿潴留等);(5)妊娠妇女或哺乳期妇女;(6)慢性酗酒史或滥用药物史或任何影响依从性的因素;(7)合并有严重心、脑血管、肝、肾和造血系统、消化性溃疡等原发性疾病者;(8)肝肾功能异常:肝(ALT或AST)超过正常值上限一倍以上或肾功能(BUN或Cr)异常者;(9)精神病患者;(10)1个月内参加过其它临床试验者;(11)研究者认为不适入选的其他情况。 |
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Exclusion criteria: |
( 1 ) Patients with dry bronchiectasis characterized by hemoptysis ; ( 2 ) Patients who have experienced changes in their condition within 4 weeks before enrollment ; ( 3 ) Special bronchiectasis patients such as nontuberculous mycobacteria ( NTM ) and allergic bronchopulmonary aspergillosis ( ABPA ) ; ( 4 ) Patients who were allergic to tiotropium bromide or had drug contraindications ( such as narrow angle glaucoma, severe prostate hyperplasia, bladder neck stenosis and urinary retention ) ; ( 5 ) pregnant women or lactation women ; ( 6 ) chronic alcohol abuse history or drug abuse history or any factor affecting compliance ; ( 7 ) Those with serious heart, cerebrovascular, liver, kidney and hematopoietic system, peptic ulcer and other primary diseases ; ( 8 ) Abnormal liver and kidney function : liver ( ALT or AST ) more than double the upper limit of normal value or abnormal renal function ( BUN or Cr ) ; ( 9 ) Psychiatric patients ; ( 10 ) Having participated in other clinical trials within one month ; ( 11 ) Other situations that the researchers think are not suitable for inclusion. |
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研究实施时间: Study execute time: |
从 From 2022-01-27 00:00:00至 To 2023-02-28 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2022-02-26 00:00:00 至 To 2022-12-31 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: |
尚未开始 Not yet recruiting |
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): |
由临床试验统计单位负责,通过SPSS生成随机数字分组表后进行分组 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Responsible for clinical trial statistics, through SPSS to generate random number grouping table after grouping |
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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: |
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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 |
否No |
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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): |
通过Excel表格整理后共享 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Shared by Excel |
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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: |
数据采集为病例记录表;数据管理为Excel表格 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Data collection for case records ; data management for Excel tables |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |