穴药调治滑胎再孕前肾虚血瘀型薄型子宫内膜的前瞻性、多中心、对照、真实世界临床研究

注册号:

Registration number:

ChiCTR2200062697 

最近更新日期:

Date of Last Refreshed on:

2023-04-06 18:24:16 

注册时间:

Date of Registration:

2022-08-15 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

穴药调治滑胎再孕前肾虚血瘀型薄型子宫内膜的前瞻性、多中心、对照、真实世界临床研究

Public title:

Prospective, multicenter, controlled, real-world clinical study on acupoint application combined with traditional Chinese medicine in the treatment of thin endometrium of kidney deficiency and blood stasis type before habitual abortion pregnancy

注册题目简写:

English Acronym:

研究课题的正式科学名称:

穴药调治滑胎再孕前肾虚血瘀型薄型子宫内膜的前瞻性、多中心、对照、真实世界临床研究

Scientific title:

Prospective, multicenter, controlled, real-world clinical study on acupoint application combined with traditional Chinese medicine in the treatment of thin endometrium of kidney deficiency and blood stasis type before habitual abortion pregnancy

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:

ChiMCTR2200006496

申请注册联系人:

黄玉 

研究负责人:

姜丽娟 

Applicant:

Yu Huang 

Study leader:

Lijuan Jiang 

申请注册联系人电话:

Applicant telephone:

+86 15808711207

研究负责人电话:

Study leader's
telephone:

+86 13668781266

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:

huangyu_km@163.com

研究负责人电子邮件:

Study leader's E-mail:

Jianglijuan0825@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:

云南省昆明市华晨路1号

研究负责人通讯地址:

云南省昆明市华晨路1号

Applicant address:

1 Huachen Road, Kunming, Yunnan

Study leader's address:

1 Huachen Road, Kunming, Yunnan

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:

云南中医药大学第一附属医院(云南省中医医院)

Applicant's institution:

Yunnan Provincial Hospital of Traditional Chinese Medicine

研究负责人所在单位:

云南中医药大学第一附属医院(云南省中医医院)

Affiliation of the Leader:

Yunnan Provincial Hospital of Traditional Chinese Medicine

是否获伦理委员会批准:

Approved by ethic committee:

Yes

伦理委员会批件文号:

Approved No. of ethic committee:

YL[2022]伦审字(017)-02

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:

云南省中医医院医学伦理委员会

Name of the ethic committee:

Medical Ethics Committee of Yunnan Provincial Hospital of Traditional Chinese Medicine

伦理委员会批准日期:

Date of approved by ethic committee:

2022-06-10 00:00:00

伦理委员会联系人:

马军

Contact Name of the ethic committee:

Jun Ma

伦理委员会联系地址:

云南省昆明市五华区光华街120号

Contact Address of the ethic committee:

120 Guanghua Street, Wuhua District, Kunming, Yunnan

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:

云南省中医医院

Primary sponsor:

Yunnan Provincial Hospital of Traditional Chinese Medicine

研究实施负责(组长)单位地址:

云南省昆明市华晨路1号

Primary sponsor's address:

1 Huachen Road, Kunming, Yunnan

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

云南

市(区县):

昆明

Country:

China

Province:

Yunnan

City:

Kunming

单位(医院):

云南省中医医院

具体地址:

云南省昆明市华晨路1号

Institution
hospital:

Yunnan Provincial Hospital of Traditional Chinese Medicine

Address:

1 Huachen Road, Kunming, Yunnan

经费或物资来源:

云南省科技厅重大科技专项计划项目(项目编号:202102AA100008)

Source(s) of funding:

Major Science and Technology Special Plan Project of Yunnan Provincial Department of Science and Technology (Project No.: 202102AA100008)

研究疾病:

滑胎再孕前肾虚血瘀型薄型子宫内膜  

Target disease:

thin endometrium of kidney deficiency and blood stasis type before habitual abortion pregnancy

研究疾病代码:

Target disease code:

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

其它 

Study phase:

N/A

研究设计:

非随机对照试验 

Study design:

Non randomized control 

研究目的:

评估穴位贴敷联合助孕养膜和畅方调治滑胎再孕前肾虚血瘀型薄型子宫内膜的临床疗效及安全性。  

Objectives of Study:

To evaluate the clinical efficacy and safety of acupoint application combined with Zhuyun Yangmo Hechang Prescription in the treatment of thin endometrium of kidney deficiency and blood stasis type before habitual abortion pregnancy.

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

Inclusion criteria

排除标准:

1.生殖器官先天畸形或有器质性病变者,如子宫纵隔、残角子宫、卵巢囊肿等影响卵泡发育、排卵者;
2.下丘脑、垂体因素影响卵泡发育、排卵者;
3.恶性肿瘤造成的卵巢组织破坏,放射、手术或炎症对卵巢的损害,影响卵泡发育、排卵者;
4.有严重的心血管、肝、肾及全身性严重疾病者;
5.意识模糊不清、无法准确表达不适症状者;
6.已知对研究药物(包括本研究药物辅料)或其类似物过敏者,或过敏体质者(如对两种或两种以上药物、食物和花粉过敏者);
7.敏感性皮肤、皮肤过敏症、急/慢性荨麻疹等皮肤疾病患者;

Exclusion criteria:

1. Congenital malformations or organic diseases of reproductive organs, such as uterine mediastinum, residual horn uterus, ovarian cyst, etc., which affect follicular development and ovulation;
2. Hypothalamic and pituitary factors affect follicular development and ovulation;
3. Ovarian tissue damage caused by malignant tumors, radiation, surgery or inflammation damage to the ovary, affecting follicular development and ovulation;
4. Have serious cardiovascular, liver, kidney and systemic diseases;
5. Vague consciousness and unable to accurately express discomfort symptoms;
6. Those who are known to be allergic to the study drug (including the excipients of the study drug) or its analogues, or those with allergic constitution (such as those who are allergic to two or more drugs, food and pollen);
7. Patients with sensitive skin, skin allergy, acute / chronic urticaria and other skin diseases.

研究实施时间:

Study execute time:

From 2022-08-01 00:00:00 To 2023-12-31 00:00:00  

征募观察对象时间:

Recruiting time:

From 2022-08-01 00:00:00 To 2023-09-30 00:00:00

干预措施:

Interventions:

组别:

试验组

样本量:

150

Group:

Test group

Sample size:

干预措施:

穴位敷贴联合助孕养膜和畅方

干预措施代码:

Intervention:

acupoint application combined with Zhuyun Yangmo Hechang Prescription

Intervention code:

组别:

对照组

样本量:

150

Group:

control group

Sample size:

干预措施:

助孕养膜和畅方

干预措施代码:

Intervention:

Zhuyun Yangmo Hechang Prescription

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

云南 

市(区县):

昆明 

Country:

China

Province:

Yunnan

City:

Kunming

单位(医院):

云南省中医医院 

单位级别:

三级甲等 

Institution
hospital:

Yunnan Provincial Hospital of Traditional Chinese Medicine

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

云南 

市(区县):

昭通 

Country:

China

Province:

Yunnan

City:

Kunming

单位(医院):

昭通市中医医院 

单位级别:

三级甲等 

Institution
hospital:

Zhaotong Hospital of Traditional Chinese Medicine

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

云南 

市(区县):

普洱 

Country:

China

Province:

Yunnan

City:

Pu'er

单位(医院):

普洱市中医医院 

单位级别:

三级甲等 

Institution
hospital:

Pu'er Hospital of Traditional Chinese Medicine

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

云南 

市(区县):

腾冲 

Country:

China

Province:

Yunnan

City:

Tengchong

单位(医院):

腾冲市中医医院 

单位级别:

二级甲等 

Institution
hospital:

Tengchong Hospital of Traditional Chinese Medicine

Level of the institution:

Secondary A

国家:

中国

省(直辖市):

云南 

市(区县):

宣威 

Country:

China

Province:

Yunnan

City:

Xuanwei

单位(医院):

宣威市中医院 

单位级别:

三级甲等 

Institution
hospital:

Xuanwei Hospital of Traditional Chinese Medicine

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

中医临床症状积分

指标类型:

主要指标

Outcome:

TCM clinical symptom score

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

子宫内膜厚度

指标类型:

次要指标

Outcome:

Endometrial thickness

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

子宫内膜分型

指标类型:

次要指标

Outcome:

Endometrial typing

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

子宫内膜血流参数指标(子宫动脉PI、RI、S/D)

指标类型:

次要指标

Outcome:

Endometrial blood flow parameters (uterine artery PI, RI, S/D)

Type:

Secondary 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:

血液

组织:

Sample Name:

Blood

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 years
最大 Max age years

性别:

女性

Gender:

Female

随机方法(请说明由何人用什么方法产生随机序列):

非随机

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

Non random

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

否No

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):

暂未确定

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

Not yet

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:

暂未确定

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

Not yet

数据与安全监察委员会:

Data and Safety Monitoring Committee:

无/No

注册人:

Name of Registration:

 2022-08-15 23:45:54