注册号: Registration number: |
ChiCTR-IPR-15006847 |
最近更新日期: Date of Last Refreshed on: |
2018-10-28 |
注册时间: Date of Registration: |
2015-05-18 |
注册号状态: |
补注册 |
Registration Status: |
Retrospective registration |
注册题目: |
玉屏风颗粒治疗小儿反复呼吸道感染安全性和有效性的随机、双盲、阳性药和安慰剂平行对照、多中心临床试验 |
Public title: |
The Safety and Efficacy of Yu Ping Feng Granule on Children with Recurrent Respiratory Tract Infections: A Multicenter, Randomized, Double-Blind, Three-arm Trial |
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: |
玉屏风颗粒治疗小儿反复呼吸道感染安全性和有效性的随机、双盲、阳性药和安慰剂平行对照、多中心临床试验 |
Scientific title: |
The Safety and Efficacy of Yu Ping Feng Granule on Children with Recurrent Respiratory Tract Infections: A Multicenter, Randomized, Double-Blind, Three-arm Trial |
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: |
申请注册联系人: |
袁丰瑞 |
研究负责人: |
申昆玲 |
Applicant: |
Yuan fengrui |
Study leader: |
Shen Kunling |
申请注册联系人电话: Applicant telephone: |
+86 0757 88333128 |
研究负责人电话: Study leader's telephone: |
+86 010-59616629 |
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: |
yuanfengrui@china-tcm.com.cn |
研究负责人电子邮件: Study leader's E-mail: |
kunlingshen1717@163.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: |
广东省佛山市顺德区容桂高新技术园科苑横四路1号 |
研究负责人通讯地址: |
北京西城区南礼士路56号 |
Applicant address: |
1 Fouth Cross Ke-Yuan Road, Shunde District, Foshan, Guangdong, China |
Study leader's address: |
56 South Lishi Road, Xicheng District, Beijing, China |
申请注册联系人邮政编码: Applicant postcode: |
528303 |
研究负责人邮政编码: Study leader's postcode: |
100045 |
申请人所在单位: |
中国医药集团中国中药有限公司 |
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Applicant's institution: |
China TCM Co., Ltd |
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: |
[2014]-Y-004-C |
伦理委员会批件附件: Approved file of Ethical Committee: |
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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儿童医院医学伦理委员会 |
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Name of the ethic committee: |
Medical ethic committee of Beijing Children Hospital, Capital Medical University |
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伦理委员会批准日期: Date of approved by ethic committee: |
2014-12-09 | ||
伦理委员会联系人: |
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Contact Name of the ethic committee: |
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伦理委员会联系地址: |
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Contact Address of the ethic committee: |
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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儿童医院 |
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Primary sponsor: |
Beijing Children Hospital, Capital Medical University |
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研究实施负责(组长)单位地址: |
北京市西城区南礼士路56号 |
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Primary sponsor's address: |
56 South Lishi Road, Xicheng 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: |
中国中药有限公司 |
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Source(s) of funding: |
China TCM Co., Ltd |
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研究疾病: |
小儿反复呼吸道感染 |
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Target disease: |
Recurrent Respiratory Tract Infections in Children |
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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 | ||||||||||||||||||||||||||||||||||||||||||||
Study phase: |
4 |
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研究目的: |
1.评价玉屏风颗粒减少小儿反复呼吸道感染的次数和改善病情作用; 2.评价玉屏风颗粒治疗小儿反复呼吸道感染表虚不固证的中医证候改善作用; 3.观察玉屏风颗粒临床应用的安全性。 |
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Objectives of Study: |
To evaluate the effectiveness and safety of Yu Ping Feng granule on children with RRTI. |
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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.符合小儿反复呼吸道感染西医诊断标准; 2.非急性感染期患儿,或急性感染期恢复后≥1周; 3.符合中医表虚不固证辨证标准; 4.年龄在2~6岁; 5.家长或监护人签署了知情同意书。 |
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Inclusion criteria |
1. Subjects are diagnosed as pediatric recurrent respiratory tract infections; 2. Subjects are not in acute infection or recovered from acute infection no less than 1 week; 3. The symptoms of subjects are in accordance to the traditional Chinese medicine syndrome category; 4. Age between 2 to 6; 5. Informed consent forms must be signed by parents or legal guardians of the subjects. |
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排除标准: |
1.原发性免疫缺陷病、先天性呼吸道畸形、先天性心脏病、胃食管反流症(GERD)、肺发育异常等基础疾病引起的呼吸道感染; 2.近1月内用过免疫抑制剂或免疫增强剂,以及服用其他治疗反复呼吸道感染药物者; 3.严重营养不良、佝偻病、贫血、支气管哮喘患者及合并心、脑、肝、肾及造血等系统严重原发性疾病者;其中ALT>1.5N(N为正常值上限)者; Cr>正常值上限者; 4.对试验用药过敏或过敏体质者(对两种及以上食物或药物过敏者); 5.研究者认为存在任何不适合入选或者影响参与或完成研究因素的患者; 6.3个月内参加其他临床试验者。 |
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Exclusion criteria: |
1. Patients with respiratory infection caused by primary immunodeficiency disease, congenital pulmonary airway malformation, gastroesophageal reflux disease (GERD), and pulmonary dysplasia; 2. Used immunosuppressants or immunoenhancive drug within 1 month, or use other treatments for RRTI; 3. Patients with severe malnutrition, rickets, anemia, asthma, and/or other vital organ disease, including those ALT level exceed 1.5 times than normal upper limit, or Cr level exceed normal upper limit; 4. Patients who are allergic to the experimental drug or allergic to more than one food or drugs; 5. Subjects who Deemed to be not appropriate to attend the trial or having problem completing the trial; 6. Subjects who attended other clinical trials within 3 monthes. |
研究实施时间: Study execute time: |
从From2014-09-16至To 2016-09-15 |
征募观察对象时间: Recruiting time: |
从From2014-09-17至To 2016-01-28 |
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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