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注册号: Registration number: |
ChiCTR2000040794 |
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最近更新日期: Date of Last Refreshed on: |
2021-04-11 01:59:34 |
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注册时间: Date of Registration: |
2020-12-10 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: |
YZJ-1139片治疗原发性慢性失眠症有效性和安全性的随机、双盲、安慰剂平行对照、多中心、Ⅱ期临床试验 |
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Public title: |
YZJ - 1139 pieces of treatment of chronic insomnia efficacy and safety of the parallel randomized, double blind, placebo controlled, multicenter, phase II clinical trials |
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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: |
YZJ-1139片治疗原发性慢性失眠症有效性和安全性的随机、双盲、安慰剂平行对照、多中心、Ⅱ期临床试验 |
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Scientific title: |
YZJ - 1139 pieces of treatment of chronic insomnia efficacy and safety of the parallel randomized, double blind, placebo controlled, multicenter, phase II clinical trials |
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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: |
江涛涛 |
研究负责人: |
江涛涛 |
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Applicant: |
TAOTAO JIANG |
Study leader: |
TAOTAO JIANG |
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申请注册联系人电话: Applicant telephone: |
+86 18019115273 |
研究负责人电话:
Study leader's |
+86 18019115273 |
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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: |
taotaoj@haiyapharma.com |
研究负责人电子邮件: Study leader's E-mail: |
taotaoj@haiyanpharma.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: |
上海市自由贸易试验区李冰路67弄8号 |
研究负责人通讯地址: |
上海市自由贸易试验区李冰路67弄8号 |
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Applicant address: |
8 Lane 67th, Libing Road, Shanghai Pilot Free Trade Zone, Shanghai, China |
Study leader's address: |
8 Lane 67th, Libing Road, Shanghai Pilot Free Trade Zone, Shanghai, China |
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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: |
上海海雁医药科技有限公司 |
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Applicant's institution: |
Shanghai Haiyan Medical Technology Co., LTD |
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研究负责人所在单位: |
上海海雁医药科技有限公司 |
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Affiliation of the Leader: |
Shanghai Haiyan Medical Technology Co., LTD |
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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: |
2019PHA027-003 |
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: |
北京大学人民医院伦理审查委员会 |
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Name of the ethic committee: |
Ethics Review Committee of Peking University People's Hospital |
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伦理委员会批准日期: Date of approved by ethic committee: |
2020-03-17 00:00:00 | ||
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伦理委员会联系人: |
王方 |
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Contact Name of the ethic committee: |
FANG WANG |
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伦理委员会联系地址: |
北京市西城区西直门南大街11号 |
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Contact Address of the ethic committee: |
11 Xizhimen Street South, Xicheng District, Beijing, 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: |
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研究实施负责(组长)单位: |
北京大学人民医院 |
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Primary sponsor: |
Peking University People's Hospital |
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研究实施负责(组长)单位地址: |
北京市西直门南大街11号北京人民大学住院部C区12层睡眠中心1207室 |
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Primary sponsor's address: |
Room 1207, Sleep Center, 12th Floor, Area C, Inpatient Department, Renmin University, 11 Xizhimen Street South, 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: |
有外部资助 |
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Source(s) of funding: |
With external funding |
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研究疾病: |
失眠 |
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Target disease: |
insomnia |
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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: |
II期临床试验 | ||||||||||||||||||||||
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Study phase: |
2 |
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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: |
主要目的:本研究的主要目的是评估YZJ-1139片短期治疗原发性慢性失眠症的有效性和安全性,探索最佳有效剂量,为Ⅲ期临床试验提供依据。 次要目的:评估YZJ-1139片治疗原发性慢性失眠症的疗效反弹、撤药反应。 |
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Objectives of Study: |
The main purpose, The main purpose of this study was to evaluate the YZJ - 1139 short-term efficacy and safety of the treatment of chronic insomnia, explore the best effective dose, provide the basis for Ⅲ stage of clinical trials.A secondary purpose, To evaluate the rebound and withdrawal response of yZJ-1139 tablets in the treatment of primary chronic insomnia. |
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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. 与神经疾病相关的睡眠障碍,如抑郁、焦虑、痴呆所致睡眠障碍;抑郁:HAMD抑郁量表评分≥18分或项目#3(自杀意念)评分为3 分及以上;焦虑:HAMA焦虑量表评分≥14分;痴呆:MMSE量表评分小学程度≤20分,中学程度(包括中专)≤22分,大学程度(包括大专)≤23分。 |
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Exclusion criteria: |
1. Sleep disorders associated with neurological disease, such as depression, anxiety, and dementia; Depression: HAMD score >=18 or item 3 (suicidal idea) score 3 or aboveAnxiety: HAMA score >=14; Dementia: MMSE score <=20 for primary school education, <=22 for secondary school education (including technical secondary school education), <=23 for university education (including junior college education); |
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研究实施时间: Study execute time: |
从 From 2019-04-01 00:00:00至 To 2020-10-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2019-06-26 00:00:00 至 To 2020-08-24 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): |
统计师编盲 |
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Randomization Procedure (please state who generates the random number sequence and by what method): |
The statistician was blind |
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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: |
Not stated |
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Blinding: |
Not stated |
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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): |
CDE |
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The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
CDE |
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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 |
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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 |