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注册号: Registration number: |
ChiCTR2200066348 |
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最近更新日期: Date of Last Refreshed on: |
2023-06-11 16:07:18 |
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注册时间: Date of Registration: |
2022-12-01 00:00:00 |
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注册号状态: |
补注册 |
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Registration Status: |
Retrospective registration |
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注册题目: |
一项评价吸入用盐酸氨溴索溶液改善(成人)下呼吸道感染疾病粘痰症状的有效性和安全性的随机、双盲、安慰剂平行对照、多中心的临床研究 |
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Public title: |
A randomized, double-blind, placebo-controlled, multicenter clinical study to evaluate the efficacy and safety of inhaled ambroxol hydrochloride solution in improving sputum property of (adult) lower respiratory tract infections |
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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: |
一项评价吸入用盐酸氨溴索溶液改善(成人)下呼吸道感染疾病粘痰症状的有效性和安全性的随机、双盲、安慰剂平行对照、多中心的临床研究 |
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Scientific title: |
A randomized, double-blind, placebo-controlled, multicenter clinical study to evaluate the efficacy and safety of inhaled ambroxol hydrochloride solution in improving sputum property of (adult) lower respiratory tract infections |
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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: |
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申请注册联系人: |
杨凯 |
研究负责人: |
陈荣昌 |
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Applicant: |
Kai Yang |
Study leader: |
Rongchang Chen |
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申请注册联系人电话: Applicant telephone: |
+86 188 4589 2814 |
研究负责人电话:
Study leader's |
+86 139 0227 3260 |
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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: |
yang.kai@szhospital.com |
研究负责人电子邮件: Study leader's E-mail: |
chenrc@vip.163.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: |
广东省深圳市罗湖区东门北路1017号 |
研究负责人通讯地址: |
广东省深圳市罗湖区东门北路1017号 |
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Applicant address: |
1017, Dongmen North Road, Luohu District, Shenzhen, Guangdong |
Study leader's address: |
1017, Dongmen North Road, Luohu District, Shenzhen, Guangdong |
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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: |
深圳市人民医院 |
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Applicant's institution: |
Shenzhen people's hospital |
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研究负责人所在单位: |
广州医科大学附属第一医院/深圳市人民医院 |
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Affiliation of the Leader: |
First Affiliated Hospital of Guangzhou Medical University/Shenzhen people's hospital |
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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: |
伦理[2017]-药物-028-02 |
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: |
广州医科大学附属第一医院医学伦理委员会 |
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Name of the ethic committee: |
Ethics Committee of First Affiliated Hospital of Guangzhou Medical University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2017-12-28 00:00:00 | ||
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伦理委员会联系人: |
余达加 |
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Contact Name of the ethic committee: |
Dajia Yu |
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伦理委员会联系地址: |
广东省广州市越秀区沿江西路151号 |
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Contact Address of the ethic committee: |
151, Yanjiang West Road, Yuexiu District, Guangzhou, Guangdong |
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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: |
广州医科大学附属第一医院 |
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Primary sponsor: |
First Affiliated Hospital of Guangzhou Medical University |
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研究实施负责(组长)单位地址: |
广东省广州市越秀区沿江西路151号 |
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Primary sponsor's address: |
151, Yanjiang West Road, Yuexiu District, Guangzhou, Guangdong |
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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: |
银谷制药有限责任公司 |
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Source(s) of funding: |
Yingu Pharmaceutical Co Ltd |
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研究疾病: |
下呼吸道感染疾病 |
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Target disease: |
Lower respiratory tract infections |
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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: |
III期临床试验 | ||||||||||||||||||||||
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Study phase: |
3 |
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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: |
评价吸入用盐酸氨溴索溶液改善下呼吸道感染疾病粘痰症状的有效性和安全性。 |
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Objectives of Study: |
To evaluate the efficacy and safety of inhaled ambroxol hydrochloride solution in improving sputum property of lower respiratory tract infections. |
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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: |
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Inclusion criteria |
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排除标准: |
1. 已知对试验用药物所含成分过敏者; |
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Exclusion criteria: |
1. Those who are known to be allergic to the ingredients contained in the experimental drug; 2. Patients with pulmonary tuberculosis, pneumoconiosis, lung cancer, pulmonary interstitial disease, bronchial asthma, Bronchiectasis with hemoptysis, pulmonary interstitial fibrosis and other serious respiratory diseases; 3. Patients with severe cardiovascular, cerebrovascular, liver, kidney, and hematopoietic system primary diseases; Alanine Transaminase ALT, Asparagus cochinchinensis aminotransferase AST are greater than 1.5 times the upper limit of normal value, and serum creatinine Cr is greater than the upper limit of normal value (refer to the normal value range of laboratory examination in the center); Fever accompanied by clear symptoms of bacterial infection, with a white blood cell count greater than 1.5 times the upper limit of normal; 4. Patients who are addicted to alcohol or drugs, have a history of epilepsy or are accompanied by mental disorders; 5. Pregnant, lactating women or those planning to conceive (including men and women); 6. Those who have participated or are currently participating in other clinical trials within 3 months; 7. Patients with thick sputum caused by airway stenosis and difficulty in coughing up (such as a history of respiratory tumors, foreign body obstruction, etc.); 8. Those who are combined with cerebrovascular accidents, cachexia, severe consumptive diseases, muscle weakness, and long-term bed rest, resulting in weak or unable to expectorate phlegm, as well as other sputum that cannot be expectorated and require nebulized inhalation or tracheotomy for sputum discharge; 9. Those who cannot cooperate with nebulization inhalation therapy or require physical expectoration; 10. Other patients who the researchers believe are not suitable for the trial. |
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研究实施时间: Study execute time: |
从 From 2017-03-01 00:00:00至 To 2020-12-22 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2018-04-10 00:00:00 至 To 2020-11-16 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: |
结束 /Completed |
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): |
由独立于本试验之外的统计师使用SAS9.4按照试验组:对照组 1:1的比例,用区组随机化方法产生随机数,将受试者随机分入试验组和对照组。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
The statisticians independent of this trial use SAS9.4 to generate random numbers by block randomization method according to the 1:1 ratio of treatment group to control group, and randomly divide the subjects into treatment group and control group. |
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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: |
不公开/Private |
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盲法: |
无 |
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Blinding: |
None |
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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): |
临床试验公共管理平台(http://www.medresman.org.cn/login.aspx) |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
Resman(http://www.medresman.org.cn/login.aspx) |
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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: |
电子采集和管理系统 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
EDC |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |