ChiCTR2000033404 版本V1.0 版本创建时间2020/05/31 14:46:25 中国临床试验注册中心

审核状态:

Project audit state:

通过审核

Successful

注册号:

Registration number:

ChiCTR2000033404 

最近更新日期:

Date of Last Refreshed on:

2020-05-31 14:46:20 

注册时间:

Date of Registration:

1990-01-01 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

待编辑(五)乌梅丸方对早醒型失眠患者肠道菌群的调节和临床疗效的研究

Public title:

The clinical efficacy research and Intestinal flora of WuMeiWan Decoction in treatment of early awakening insomnia

注册题目简写:

English Acronym:

研究课题的正式科学名称:

乌梅丸方对早醒型失眠患者肠道菌群的调节和临床疗效的研究

Scientific title:

The clinical efficacy research and Intestinal flora of WuMeiWan Decoction in treatment of early awakening insomnia

研究课题代号(代码):

Study subject ID:

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:

朱晓松 

研究负责人:

朱晓松 

Applicant:

Zhu Xiaosong 

Study leader:

Zhu xiaosong 

申请注册联系人电话:

Applicant telephone:

15106677973

研究负责人电话:

Study leader's telephone:

15106677973

申请注册联系人传真 :

Applicant Fax:

研究负责人传真:

Study leader's fax:

申请注册联系人电子邮件:

Applicant E-mail:

zxs_sdu@163.com

研究负责人电子邮件:

Study leader's E-mail:

zxs_sdu@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):

申请注册联系人通讯地址:

山东省临沂市兰山区解放路东段27号

研究负责人通讯地址:

山东省临沂市兰山区解放路东段27号

Applicant address:

No. 27 Eastern Section of Jiefang Rd, Lanshan district, Linyi City, Shandong Prov

Study leader's address:

No. 27 Eastern Section of Jiefang Rd, Lanshan district, Linyi City, Shandong Prov

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:

申请人所在单位:

临沂市人民医院

Applicant's institution:

Linyi City People's Hospital

研究负责人所在单位:

临沂市人民医院

Affiliation of the Leader:

Linyi City People's Hospital

是否获伦理委员会批准:

是/Yes

Approved by ethic committee:

Yes

伦理委员会批件文号:

Approved No. of ethic committee:

YX15001

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:

临沂市人民医院伦理委员会

Name of the ethic committee:

Ethics Committee of Linyi City People's Hospital

伦理委员会批准日期:

Date of approved by ethic committee:

2020-05-21 00:00:00

伦理委员会联系人:

肖帅

Contact Name of the ethic committee:

Xiao Shuai

伦理委员会联系地址:

山东省临沂市兰山区解放路东段27号

Contact Address of the ethic committee:

No. 27 Eastern Section of Jiefang Rd, Lanshan district, Linyi City, Shandong Prov

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:

临沂市人民医院

Primary sponsor:

Linyi City People's Hospital

研究实施负责(组长)单位地址:

山东省临沂市兰山区解放路东段27号

Primary sponsor's address:

No. 27 Eastern Section of Jiefang Rd, Lanshan district, Linyi City, Shandong Prov

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

山东

市(区县):

临沂

Country:

China

Province:

Shandong

City:

Linyi

单位(医院):

临沂市人民医院

具体地址:

兰山区解放路东段27号

Institution
hospital:

Linyi City People's Hospital

Address:

27 East Section of Jiefang Road, Lanshan District

经费或物资来源:

山东省中医药科技发展项目医院配资

Source(s) of funding:

Shandong TCM science and technology development project hospital funding

Target disease:

early awakening insomnia

Target disease code:

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

I期临床试验 

Study phase:

1

研究设计:

病例对照研究 

Study design:

Case-Control study 

研究目的:

观察乌梅丸治疗早醒型失眠的临床疗效及对患者肠道菌群的影响。  

Objectives of Study:

To observe The clinical efficacy research and Intestinal flora of WuMeiWan Decoction in treatment of early awakening insomnia

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

(1)符合西医失眠症的诊断标准
(2)符合早醒的临床表现:睡眠觉醒时间较正常时间提前30min以上,甚至比平时早醒1~2h,总的睡眠时间少于6h;包括以下1至数项:四肢厥冷、巅顶疼痛、口渴、饥不欲食、心烦及躁动不安等寒热错杂之象。
(3)PSQI总分>7分;
(4)年龄在18岁~60之间,男女不限;
(5)了解本项药物的临床观察意义,对从事该项的研究人员的临床随访及临床评价积极配合,依从性好;
(6)病人在完全知情的情况下自愿参加本研究;
(7)3个月内未应用损伤肝功、肾功的药物者;
(8)3个月以内否认参加过其它治疗受试患者;
(9)一周内没有服用过镇静安神药物;
(10)意识清楚,同意及能够配合采集临床资料者

Inclusion criteria

(1) in line with the western medicine diagnostic criteria for insomnia
(2) in accordance with the clinical manifestations of early awakening: sleep awakening time than normal time above 30 min in advance, or wake up earlier than usual 1 ~ 2 h, the total sleep time is less than 6 h; Includes the following 1 to several items: extremities cold, apex pain, thirst, hunger, restlessness and restlessness.
(3) the total PSQI score was > and 7;
(4) between the ages of 18 and 60, both male and female;
(5) to understand the clinical observation significance of this drug, actively cooperate with the clinical follow-up and clinical evaluation of the researchers engaged in this drug, and have good compliance;
(6) patients voluntarily participate in this study with full knowledge;
(7) drugs that damage liver and kidney functions have not been applied within 3 months;
(8) denied participating in other treatments within 3 months;
(9) have not taken any sedatives within one week;
(10) those who are conscious, agree and able to cooperate in collecting clinical data.

排除标准:

(1)凡不符合纳入标准者;
(2)以多梦、睡眠浅社会功能受损为主诉的失眠患者;
(3)排除继发性失眠:失眠因全身性疾患如疼痛、发热、咳嗽、手术、受外界干扰等,以及躯体性疾病或精神障碍性疾病引起的失眠,如:抑郁症;焦虑症;精神疾病患者;
(4)合并有心、脑血管,肺、肝、肾和造血系统等严重原发性和严重器质性疾病患者;
(5)过敏体质的患者;
(6)妊娠期及哺乳期的妇女;
(7)有酗酒和药物依赖及滥用药物的患者;
(8)失代偿的呼吸功能不全患者,重症肌无力、重症睡眠呼吸暂停综合症患者

Exclusion criteria:

(1) those failing to meet the inclusion criteria;
(2) patients with insomnia who complained of multiple dreams and impaired shallow social function;
(3) excluding secondary insomnia: insomnia caused by systemic diseases such as pain, fever, cough, surgery, external interference, etc., as well as insomnia caused by physical diseases or mental disorders, such as depression; Anxiety disorder; People with mental illness;
(4) patients with serious primary and serious organic diseases including heart, cerebrovascular, lung, liver, kidney and hematopoietic system;
(5) patients with allergic constitution;
(6) women during pregnancy and lactation;
(7) patients with alcohol and drug dependence and substance abuse;
(8) patients with decompensated respiratory dysfunction, myasthenia gravis and severe sleep apnea

研究实施时间:

Study execute time:

From 2020-01-01 00:00:00 To 2021-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2020-07-01 00:00:00 To 2021-06-30 00:00:00  

干预措施:

Interventions:

组别:

健康人

样本量:

20

Group:

Normal group

Sample size:

干预措施:

干预措施代码:

Intervention:

no

Intervention code:

组别:

疾病组

样本量:

20

Group:

Disease group

Sample size:

干预措施:

乌梅丸治疗

干预措施代码:

Intervention:

treat with Wumeiwan

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

山东 

市(区县):

 

Country:

China 

Province:

Shandong 

City:

 

单位(医院):

临沂市人民医院 

单位级别:

三甲 

Institution
hospital:

Linyi City People's Hospital

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

肠道菌群

指标类型:

主要指标

Outcome:

intestinal flora

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

匹兹堡睡眠质量指数量表

指标类型:

主要指标

Outcome:

PSQI

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

中医生活质量量表

指标类型:

主要指标

Outcome:

Quality of life scale of traditional Chinese Medicine

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

采集人体标本:

Collecting sample(s)
from participants:

标本中文名:

粪便

组织:

Sample Name:

facaes

Tissue:

人体标本去向

使用后销毁  

说明

Fate of sample:

Destruction after use  

Note:

征募研究对象情况:

Recruiting status:

尚未开始

Not yet recruiting

年龄范围:

Participant age:

最小 Min age 18 years
最大 Max age 60 years

性别:

男女均可

Gender:

Both

随机方法(请说明由何人用什么方法产生随机序列):

由门诊医生随机选择

Randomization Procedure (please state who generates the random number sequence and by what method):

Randomly selected by an outpatient physician

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

盲法:

Blinding:

是否共享原始数据:

IPD sharing

Yes

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):

试验完成6个月内,中国临床试验注册中心原始数据共享平台公开, http://www.medresman.org.cn.

The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url):

The trial will be published on IPD Sharing Platform within 6 months of completion, http://www.medresman.org.cn.

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:

病例记录表

Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture:

Case Record Form, CRF

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2020-05-31 14:46:20