Clinical study of Jinshuibao Capsule to improve ivF-ET pregnancy outcome in infertile patients with renal deficiency and ovarian reserve dysfunction

注册号:

Registration number:

ITMCTR2000003948

最近更新日期:

Date of Last Refreshed on:

2020-08-25

注册时间:

Date of Registration:

2020-08-25

注册号状态:

Registration Status:

预注册

Prospective registration

注册题目:

金水宝胶囊改善肾虚型卵巢储备功能减退不孕患者IVF-ET妊娠结局的临床研究

Public title:

Clinical study of Jinshuibao Capsule to improve ivF-ET pregnancy outcome in infertile patients with renal deficiency and ovarian reserve dysfunction

注册题目简写:

English Acronym:

研究课题的正式科学名称:

金水宝胶囊改善肾虚型卵巢储备功能减退不孕患者IVF-ET妊娠结局的临床研究

Scientific title:

Clinical study of Jinshuibao Capsule to improve ivF-ET pregnancy outcome in infertile patients with renal deficiency and ovarian reserve dysfunction

研究课题的正式科学名称简写:

Scientific title acronym:

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:

ChiCTR2000036736 ; ChiMCTR2000003948

申请注册联系人:

俞瑾

研究负责人:

俞瑾

Applicant:

Jin Yu

Study leader:

Jin Yu

申请注册联系人电话:

Applicant telephone:

+86 15821627980

研究负责人电话:

Study leader's telephone:

+86 15821627980

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:

395005545@163.com

研究负责人电子邮件:

Study leader's E-mail:

395005545@163.com

申请单位网址(自愿提供):

Study leader's 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:

上海市徐汇区广元路145号

研究负责人通讯地址:

上海市徐汇区广元路145号

Applicant address:

145 Guangyuan Road, Xuhui District, Shanghai, China

Study leader's address:

145 Guangyuan Road, Xuhui District, Shanghai, China

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:

中国福利会国际和平妇幼保健院

Applicant's institution:

China Welfare Association International Peace Maternal and Child Health Hospital

是否获伦理委员会批准:

Approved by ethic committee:

伦理委员会批件文号:

Approved No. of ethic committee:

伦理委员会批件附件:

Approved file of Ethical Committee:

批准本研究的伦理委员会名称:

Name of the ethic committee:

伦理委员会批准日期:

Date of approved by ethic committee:

2013/8/26 0:00:00

伦理委员会联系人:

Contact Name of the ethic committee:

伦理委员会联系地址:

Contact Address of the ethic committee:

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:

中国福利会国际和平妇幼保健院

Primary sponsor:

China Welfare Association International Peace Maternal and Child Health Hospital

研究实施负责(组长)单位地址:

上海市徐汇区广元路145号

Primary sponsor's address:

145 Guangyuan Road, Xuhui District, Shanghai, China

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

上海

市(区县):

Country:

China

Province:

Shanghai

City:

单位(医院):

中国福利会国际和平妇幼保健院

具体地址:

徐汇区广元路145号

Institution
hospital:

China Welfare Association International Peace Maternal and Child Health Hospital

Address:

145 Guangyuan Road, Xuhui District

经费或物资来源:

申康项目

Source(s) of funding:

Shen-kang project

研究疾病:

卵巢功能减退相关性不孕症

研究疾病代码:

Target disease:

Infertility associated with ovarian dysfunction

Target disease code:

研究类型:

Study type:

干预性研究

Interventional study

研究设计:

Study design:

随机平行对照

randomized controlled trial(parallel group design)

研究所处阶段:

Study phase:

上市后药物

Post-marketing clinical trial

研究目的:

明确金水宝胶囊对DOR患者卵巢功能及IVF-ET妊娠结局的改善作用,拓展金水宝胶囊的临床应用范围。

Objectives of Study:

To clarify the improvement effect of Jinshuibao capsule on ovarian function and IVF-ET pregnancy outcome of DOR patients, and expand the scope of clinical application of Jinshuibao capsule.

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)年龄段为18到39岁; (2)同时符合DOR西医诊断标准、不孕症诊断标准及中医诊断标准; (3)均拟在中国福利会国际和平妇幼保健院生殖中心行IVF-ET 移植(采用 GnRH-a 超长方案自然周期冻融胚胎移植 D3); (4)未曾行药物治疗或曾服用药物但已停药3个月以上者; (5)自愿参加本临床研究,并签署相关知情同意书。

Inclusion criteria

(1) The age range is 18 to 39; (2) It conforms to the diagnostic criteria of western medicine and Chinese medicine at the same time; (3) All planned to perform IVF-ET transplantation in the Reproductive Center of The International Peace Maternal and Child Health Center of China Welfare Association (ADOPT GNRH-A ultra-long natural cycle freeze-thawed embryo transplantation D3); (4) those who have not taken medication or have taken medication but have stopped taking medication for more than 3 months; (5) Volunteer to participate in this clinical study and sign the relevant informed consent.

排除标准:

(1)符合IVF-ET 及其衍生技术的禁忌症中任意一条者均予以排除; (2)近3个月内应用激素类药物者; (3)排卵障碍因素、免疫因素、染色体异常因素造成不孕症者; (4)男方精液分析异常者; (5)有严重药物过敏史者; (6)合并有乳腺或其他生殖器官疾病如子宫多发肌瘤、多囊卵巢综合症、子宫内膜异位症症、生殖器官畸形或生理缺陷等患者,或同时患有严重内科疾病者等; (7)对多种药物过敏或已知对本药组成成分过敏者; (8)正参加其他临床实验项目者。

Exclusion criteria:

(1) Any contraindications in accordance with IVF-ET and its derived technologies shall be excluded; (2) Those who have used hormone drugs in recent 3 months; (3) Infertility caused by ovulation disorders, immune factors and chromosomal abnormalities; (4) Abnormal analysis of male semen; (5) Persons with a history of severe drug allergy; (6) Patients with breast or other reproductive organ diseases, such as multiple uterine fibroids, polycystic ovary syndrome, endometriosis, malformation of reproductive organs or physiological defects, or those with serious medical diseases; (7) People who are allergic to multiple drugs or have known allergies to the components of this drug; (8) Participating in other clinical trial projects.

研究实施时间:

Study execute time:

From 2020-10-01

To      2022-09-30

征募观察对象时间:

Recruiting time:

From 2020-10-01

To      2021-09-30

干预措施:

Interventions:

组别:

Group 2

样本量:

54

Group:

Group 2

Sample size:

干预措施:

辅酶Q10胶囊

干预措施代码:

Intervention:

Coenzyme Q10 capsules

Intervention code:

组别:

Group 1

样本量:

54

Group:

Group 1

Sample size:

干预措施:

金水宝胶囊

干预措施代码:

Intervention:

Jinshuibao capsule

Intervention code:

样本总量 Total sample size : 108

研究实施地点:

Countries of recruitment
and research settings:

国家:

中国

省(直辖市):

上海

市(区县):

Country:

China

Province:

Shanghai

City:

单位(医院):

中国福利会国际和平妇幼保健院

单位级别:

三级甲等专科

Institution/hospital:

China Welfare Association International Peace Maternal and Child Health Hospital

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

实验室指标

指标类型:

次要指标

Outcome:

laboratory index

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

临床症状

指标类型:

次要指标

Outcome:

clinical symptoms

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

临床妊娠率

指标类型:

主要指标

Outcome:

clinical pregnancy rate

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:

血清

组织:

Sample Name:

serum

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:

尚未开始

Not yet recruiting

年龄范围:

最小
Min age years
最大
Max age years

Recruiting status:

Participant age:

性别:

Gender:

女性

Female

随机方法(请说明由何人用什么方法产生随机序列):

本项目拟采用简单随机法,根据SAS软件产生随机数字。

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

This project intends to adopt simple random method and generate random Numbers according to SAS software.

盲法:

双盲

Blinding:

Double blind

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个月后在网络平台公开(https://pan.baidu.com/disk/home?#/all?path=%2F&vmode=list)

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

The trial was published on the network platform 6 months after completion(https://pan.baidu.com/disk/home?#/all?path=%2F&vmode=list)

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:

通过CRF表进行数据采集及管理

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

Data collection and management through CRF table

数据管理委员会:

Data Managemen Committee:

Yes

研究计划书或研究结果报告发表信息
(杂志名称、期、卷、页,时间;或网址):

Publication information of the protocol/research results report
(name of the journal, volume, issue, pages, time; or website):

ITMCTR BJ-ICP:07032215-5 Tip: IE8 is recommended Use the system with widescreen display resolution above