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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: |
ChiCTR2300067872 |
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最近更新日期: Date of Last Refreshed on: |
2023-01-30 09:41:21 |
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注册时间: Date of Registration: |
2023-01-30 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: |
评价散寒化湿颗粒与Paxlovid对照治疗轻型/中型新型冠状病毒感染有效性和安全性的随机、开放、多中心临床研究 |
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Public title: |
A randomized, controlled and open clinical study evaluating the efficacy and safety of Sanhanhuashi granules versus Paxlovid in the treatment of mild/medium-sized Covid-19 |
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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: |
评价散寒化湿颗粒与Paxlovid对照治疗轻型/中型新型冠状病毒感染有效性和安全性的随机、开放、多中心临床研究 |
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Scientific title: |
A randomized, controlled and open clinical study evaluating the efficacy and safety of Sanhanhuashi granules versus Paxlovid in the treatment of mild/medium-sized Covid-19 |
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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: |
赵宾江 |
研究负责人: |
曹彬 |
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Applicant: |
Zhao Binjiang |
Study leader: |
Cao Bin |
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申请注册联系人电话: Applicant telephone: |
+86 15300025287 |
研究负责人电话:
Study leader's |
+86 01084206264 |
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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: |
zbj287@163.com |
研究负责人电子邮件: Study leader's E-mail: |
caobin_ben@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: |
江苏省连云港市经济技术开发区江宁工业园康缘路58号 |
研究负责人通讯地址: |
北京市朝阳区樱花东街 2号 |
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Applicant address: |
58 Kangyuan Road, Jiangning Industrial Park, Economic and Technological Development Zone, Lianyun'gang, Jiangsu |
Study leader's address: |
No.2, Yinghuayuan East Street, 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: |
江苏康缘药业股份有限公司 |
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Applicant's institution: |
Jiangsu Kanion Pharmaceutical Co, Ltd. |
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研究负责人所在单位: |
中日友好医院 |
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Affiliation of the Leader: |
China-Japan Friendship 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: |
YW2023-005-01 |
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: |
中日友好医院药物临床试验伦理委员会 |
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Name of the ethic committee: |
China-Japan Friendship Hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
2023-01-18 00:00:00 | ||
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伦理委员会联系人: |
赵志霞 |
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Contact Name of the ethic committee: |
Zhao Zhixia |
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伦理委员会联系地址: |
北京市朝阳区樱花东街 2号 |
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Contact Address of the ethic committee: |
No.2, Yinghuayuan East Street, Beijing |
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伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 10 84205645 |
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: |
中日友好医院 |
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Primary sponsor: |
China-Japan Friendship Hospital |
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研究实施负责(组长)单位地址: |
北京市朝阳区樱花东街 2号 |
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Primary sponsor's address: |
No.2, Yinghuayuan East Street, 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: |
江苏康缘药业股份有限公司 |
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Source(s) of funding: |
Jiangsu Kanion Pharmaceutical Co, Ltd. |
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研究疾病: |
新型冠状病毒感染 |
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Target disease: |
Covid-19 |
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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: |
上市后药物 | ||||||||||||||||||||||
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Study phase: |
4 |
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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. 与Paxlovid对照,评价散寒化湿颗粒颗粒治疗轻型/中型新型冠状病毒感染的有效性; 2. 评价散寒化湿颗粒颗粒治疗轻型/中型新型冠状病毒感染的安全性 。 |
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Objectives of Study: |
1. evaluate the efficacy of Sanhanhuashi granules for the treatment of mild/medium-sized Covid-19 in comparison with Paxlovid. 2. To evaluate the safety of Sanhanhuashi granules in the treatment of mild/medium-sized Covid-19 . |
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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.年龄18~70周岁(包含两端),性别不限; |
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Inclusion criteria |
1.Patients aged 18-70 years (inclusive). Regardless of gender. 2. Diagnosis of COVID-19 by SARS-CoV-2 nucleic acid test/ or antigen test. 3.The subjects were classified as mild/moderate type COVID-19. 4. First onset of symptoms ≤ 72 hours from first dose of trial drug. 5. Three or more of the following symptoms: fever, stuffy or runny nose, sore throat, cough, shortness of breath or difficulty breathing, muscle or body aches, headache, malaise, nausea, vomiting, diarrhea. 6. Signed an informed consent form. |
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排除标准: |
1.经研究者判断在随机前可能进展为重型或危重型COVID-19者; |
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Exclusion criteria: |
1.investigators to be likely to progress to severe or critical COVID-19 before randomization. 2.Meets severe /critical early warning indicators. 3.Aged >65 years and not vaccinated against the Covid-19 vaccine. 4.Chronic lung disease (e.g., chronic obstructive pulmonary disease, moderate/severe asthma, interstitial lung disease, cystic fibrosis, and pulmonary hypertension) and maintenance dialysis. 5.Compromised immune system. (e.g. AIDS , long-term use of corticosteroids or other immunosuppressive drugs resulting in a hypoimmune state). 6.Obese (BMI ≥ 30 kg/m2). 7.Heavy smokers. 8.Pregnant patients, pregnant patients and breastfeeding patients. 9.Male subjects whose wives or partners are planning to become pregnant during the study period. 10.Have used the same type of proprietary Chinese medicine for more than 2 days before enrollment. 11.Treatment with antivirals against SARS-CoV-2 or SARS-CoV-2 monoclonal antibody prior to randomization. 12.Have received neutralizing antibodies or convalescent plasma therapy due to COVID-19. 13.Those who used drugs prohibited in the Paxlovid instructions before enrollment. 14.Has hypersensitivity or other contraindication to any of the components of the study interventions. 15.Those with a white blood cell count exceeding 20% of the upper limit of normal in routine blood work, or those with large amounts of pus sputum suspected of bacterial infection. 16.Previous administration with any investigational drug within 30 days before the study drug administration. 17.Patients who are considered unsuitable for clinical trials by the researcher. |
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研究实施时间: Study execute time: |
从 From 2023-01-18 00:00:00至 To 2024-01-17 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2023-01-30 00:00:00 至 To 2023-09-30 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): |
计算机分层区组随机,由统计专业人员采用SAS v9.4产生随机序列号。 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
Stratified blocked randomization procedure is provided by a professional statistician using SAS v9.4 |
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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): |
试验完结后通过论文发表形式公开 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
After the end of the trial through the publication of papers |
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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: |
本研究采用电子数据采集系统(EDC)进行数据管理。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Electronic data acquisition system (EDC) was used for data management in this study. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |