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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: |
ChiCTR2200061367 |
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最近更新日期: Date of Last Refreshed on: |
2022-06-22 01:20:40 |
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注册时间: Date of Registration: |
2022-06-22 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: |
评价玉屏通窍片治疗持续性变应性鼻炎(肺脾两虚证)有效性和安全性的多中心、随机、双盲、安慰剂平行对照Ⅲ期临床试验 |
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Public title: |
A multicenter, randomized, double-blind, placebo-controlled phase iii clinical trial to evaluate the efficacy and safety of Yuping Tongqiao Tablet in the treatment of persistent allergic rhinitis (syndrome of deficiency of lung and spleen) |
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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: |
评价玉屏通窍片治疗持续性变应性鼻炎(肺脾两虚证)有效性和安全性的多中心、随机、双盲、安慰剂平行对照Ⅲ期临床试验 |
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Scientific title: |
A multicenter, randomized, double-blind, placebo-controlled phase iii clinical trial to evaluate the efficacy and safety of Yuping Tongqiao Tablet in the treatment of persistent allergic rhinitis (syndrome of deficiency of lung and spleen) |
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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: |
ChiMCTR2200006192 |
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申请注册联系人: |
肖丽娜 |
研究负责人: |
王俊阁 |
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Applicant: |
Lina Xiao |
Study leader: |
Junge Wang |
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申请注册联系人电话: Applicant telephone: |
+86 15732190274 |
研究负责人电话:
Study leader's |
+86 18901176299 |
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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: |
xiaolina@yiling.cn |
研究负责人电子邮件: Study leader's E-mail: |
wjgent@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: |
石家庄天山大街238号 |
研究负责人通讯地址: |
北京市东城区美术馆后街 23 号 |
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Applicant address: |
238 Tianshan Street, Shijiazhuang, Hebei, China |
Study leader's address: |
23 Back Street, Art Museum, Dongcheng 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: |
北京以岭药业有限公司 |
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Applicant's institution: |
Beijing Yiling Pharmaceutical Co., Ltd |
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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: |
2022BL01-012-02 |
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: |
首都医科大学附属北京中医医院医学伦理委员会 |
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Name of the ethic committee: |
Medical Ethics Committee of Beijing Hospital of Traditional Chinese Medicine |
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伦理委员会批准日期: Date of approved by ethic committee: |
2022-05-26 00:00:00 | ||
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伦理委员会联系人: |
王晶 |
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Contact Name of the ethic committee: |
Jing Wang |
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伦理委员会联系地址: |
北京市东城区美术馆后街69号北京中医医院景美办公区113 |
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Contact Address of the ethic committee: |
113, Jingmei Office District, Beijing Hospital of Traditional Chinese Medicine, 69 Back Street of Art Museum, Dongcheng 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: |
首都中医药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 Museum Back Street, Dongcheng 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: |
北京以岭药业有限公司 |
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Source(s) of funding: |
Beijing Yiling Pharmaceutical Co., Ltd |
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研究疾病: |
持续性变应性鼻炎 |
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Target disease: |
Persistent allergic rhinitis |
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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: |
进一步评价玉屏通窍片治疗持续性变应性鼻炎(肺脾两虚证)的有效性和安全性,为申报注册提供依据。 |
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Objectives of Study: |
To further evaluate the efficacy and safety of Yuping Tongqiao tablet in the treatment of persistent allergic rhinitis (syndrome of deficiency of lung and spleen), and to provide a basis for registration. |
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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18~65周岁(含18和65周岁),性别不限; |
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Inclusion criteria |
(1) Aged between 18 and 65 (including 18 and 65), regardless of gender; |
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排除标准: |
(1)合并严重鼻中隔偏曲、鼻窦炎、鼻息肉、肥厚性鼻炎等鼻部器质性病变; |
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Exclusion criteria: |
(1) complicated with severe nasal septum deviation, sinusitis, nasal polyp, hypertrophic rhinitis and other organic lesions of the nose; |
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研究实施时间: Study execute time: |
从 From 2022-03-05 00:00:00至 To 2023-12-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2022-07-01 00:00:00 至 To 2023-07-31 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): |
本试验采用区组随机化方法,各中心竞争入组,按照2:1的比例将受试者随机分配至试验组和安慰剂组 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
This trial adopts the method of block randomization, each center competes for the group, and the subjects are randomly assigned to the experimental group and the placebo group according to the ratio of 2:1. |
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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: |
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Blinding: |
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是否共享原始数据: IPD sharing |
是Yes |
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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): |
EDC系统 请阅读网页注册指南中关于 原始数据共享 的内容 |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
EDC |
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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: |
数据资料分别采用电子版进行采集和统计。 |
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Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
The data are collected and counted in electronic version respectively. |
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数据与安全监察委员会: Data and Safety Monitoring Committee: |
无/No |