注册号: Registration number: |
ChiCTR2000029589 |
最近更新日期: Date of Last Refreshed on: |
2020-06-28 |
注册时间: Date of Registration: |
2020-02-05 |
注册号状态: |
预注册 |
Registration Status: |
Prospective registration |
注册题目: |
以常规治疗为对照,评价热毒宁注射液治疗新型冠状病毒肺炎有效性和安全性的前瞻性、随机、开放、多中心临床研究 |
Public title: |
A prospective, randomized,open, multi-center clinical trial evaluating the efficiency and safety of Reduning injection in the treatment of novel coronavirus pneumonia (COVID-19) |
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: |
以常规治疗为对照,评价热毒宁注射液治疗新型冠状病毒肺炎有效性和安全性的前瞻性、随机、开放、多中心临床研究 |
Scientific title: |
A prospective, randomized,open, multi-center clinical trial evaluating the efficiency and safety of Reduning injection in the treatment of novel coronavirus pneumonia (COVID-19) |
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: |
ChiMCTR2000002972 |
申请注册联系人: |
王辉 |
研究负责人: |
刘清泉 |
Applicant: |
Wang Hui |
Study leader: |
Liu Qingquan |
申请注册联系人电话: Applicant telephone: |
+86 13820738263 |
研究负责人电话: Study leader's telephone: |
+86 010-52176520 |
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: |
wangh@tice.com.cn |
研究负责人电子邮件: Study leader's E-mail: |
Liuqingquan2003@126.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): |
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申请注册联系人通讯地址: |
天津市静海区鄱阳湖路10号 |
研究负责人通讯地址: |
北京市东城区美术馆后街23号 |
Applicant address: |
10 Poyang Lake Road, Jinghai District, Tianjin, China |
Study leader's address: |
23 Art Gallery Back Street, Dongcheng District, Beijing, China |
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: |
天津中医药大学 |
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Applicant's institution: |
Tianjin University of Traditional Chinese Medicine |
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: |
TJUTCM-EC20200001 |
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: |
天津中医药大学医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee of Tianjin University of TCM |
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伦理委员会批准日期: Date of approved by ethic committee: |
2020-02-05 | ||
伦理委员会联系人: |
王辉 |
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Contact Name of the ethic committee: |
Wang Hui |
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伦理委员会联系地址: |
天津市静海区鄱阳湖路10号 |
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Contact Address of the ethic committee: |
10 Poyang Lake Road, Jinghai District, Tianjin, China |
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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: |
研究实施负责(组长)单位: |
首都医科大学附属北京中医医院 |
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Primary sponsor: |
Beijing hospital of Traditional Chinese Medicine |
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研究实施负责(组长)单位地址: |
北京市东城区美术馆后街23号 |
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Primary sponsor's address: |
23 Art Gallery Back Street, Dongcheng District, Beijing, China |
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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: |
自筹 |
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Source(s) of funding: |
raise independently |
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研究疾病: |
新型冠状病毒感染的肺炎(COVID-19) |
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Target disease: |
novel coronavirus pneumonia (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: |
探索性研究/预试验 | ||||||||||||||||||||||
Study phase: |
0 |
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研究目的: |
探索热毒宁注射液治疗新型冠状病毒肺炎的有效性和安全性。 |
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Objectives of Study: |
Explore the effectiveness and safety of Reduning injection in the treatment for pneumonia (common type) caused by new coronavirus (2019-nCoV). |
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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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研究设计: |
随机平行对照 |
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Study design: |
Parallel |
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纳入标准: |
(1)符合《新型冠状病毒感染的肺炎诊疗方案(试行第五版)》诊断标准; (2)临床分型为普通型、重型; (3)入组时具备发热、咳嗽、乏力中一项或一项以上症状; (4)确诊时间不超过48小时; (5)患者年龄≥18周岁。 |
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Inclusion criteria |
(1) Comply with the diagnostic criteria of "Pneumonitis Diagnosis and Treatment Scheme for New Coronavirus Infection (Trial Version 5)"; (2) The classification was judged as common and severe type; (3) Having one or more symptoms of fever, cough and fatigue when entering the group; (4) The diagnosis time does not exceed 48 hours; (5) Aged >= 18 years. |
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排除标准: |
(1)免疫缺陷疾病,或近3个月内使用免疫抑制剂或糖皮质激素者; (2)准备妊娠者、孕妇及哺乳期妇女; (3)过敏体质者(指对两种以上的药品或食品过敏或本次试验用药已知成份过敏); (4)精神病患者,或无自知能力者; (5)从筛选开始预计生存时间不超过48小时的患者; (6)筛选时已经气管插管,机械通气; (7)研究者认为有不适宜参加临床试验者。 |
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Exclusion criteria: |
(1) Immunodeficiency diseases, or those using immunosuppressive agents or glucocorticoids within the past 3 months; (2) Pregnancies, pregnant women and lactating women; (3) An allergic condition, such as a history of allergies to two or more drugs or foods, or a known allergy to the ingredients in this test); (4) Psychotic patients, or those without self-knowledge ability; (5) Patients whose estimated survival time does not exceed 48 hours from the start of screening; (6) Tracheal intubation and mechanical ventilation have been performed during screening; (7) Other problems that doctor's judgment is not suitable for the study. |
研究实施时间: Study execute time: |
从From2020-02-05至To 2021-12-31 |
征募观察对象时间: Recruiting time: |
从From2020-02-06至To 2021-12-30 |
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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