麒麟丸对体外受精-胚胎移植助孕患者妊娠结局影响的随机、双盲、安慰剂对照试验

注册号:

Registration number:

ITMCTR1900002731

最近更新日期:

Date of Last Refreshed on:

2019-11-01

注册时间:

Date of Registration:

2019-11-01

注册号状态:

Registration Status:

预注册

Prospective registration

注册题目:

麒麟丸对体外受精-胚胎移植助孕患者妊娠结局影响的随机、双盲、安慰剂对照试验

Public title:

A randomized, double-blind, placebo-controlled clinical trial to evaluate the effects of Qilin Pill on pregnancy outcomes in patients undergoing in vitro fertilization-embryo transfer

注册题目简写:

English Acronym:

研究课题的正式科学名称:

麒麟丸对体外受精-胚胎移植助孕患者妊娠结局影响的随机、双盲、安慰剂对照试验

Scientific title:

A randomized, double-blind, placebo-controlled clinical trial to evaluate the effects of Qilin Pill on pregnancy outcomes in patients undergoing in vitro fertilization-embryo transfer

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:

ChiCTR1900027111 ; ChiMCTR1900002731

申请注册联系人:

白俊

研究负责人:

贺丰杰

Applicant:

Bai Jun

Study leader:

He Fengjie

申请注册联系人电话:

Applicant telephone:

+86 15769212098

研究负责人电话:

Study leader's telephone:

+86 13892908898

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:

baijun2098@163.com

研究负责人电子邮件:

Study leader's E-mail:

hefengjie2013@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:

陕西省咸阳市秦都区渭阳西路副2号

研究负责人通讯地址:

陕西省咸阳市秦都区渭阳西路副2号

Applicant address:

2 Weiyang Road West, Qindu District, Xianyang, Shaanxi

Study leader's address:

2 Weiyang Road West, Qindu District, Xianyang, Shaanxi

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:

陕西中医药大学附属医院

Applicant's institution:

Affiliated Hospital of Shaanxi University of Chinese Medicine

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:

SZFYRMEC-PJ-2019年第【01】号

伦理委员会批件附件:

Approved file of Ethical Committee:

查看附件

批准本研究的伦理委员会名称:

陕西中医药大学附属医院生殖医学伦理委员会

Name of the ethic committee:

Reproductive Medicine Ethics Committee of Affiliated Hospital of Shaanxi University of Chinese Me

伦理委员会批准日期:

Date of approved by ethic committee:

2019/6/18 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:

陕西中医药大学附属医院

Primary sponsor:

Affiliated Hospital of Shaanxi University of Chinese Medicine

研究实施负责(组长)单位地址:

陕西省咸阳市秦都区渭阳西路副2号

Primary sponsor's address:

2 Weiyang Road West, Qindu District, Xianyang, Shaanxi

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

陕西省

市(区县):

咸阳

Country:

China

Province:

Shaanxi

City:

Xiangyang

单位(医院):

陕西中医药大学附属医院

具体地址:

秦都区渭阳西路副2号

Institution
hospital:

Affiliated Hospital of Shaanxi University of Chinese Medicine

Address:

2 Weiyang Road West, Qindu District

经费或物资来源:

重大疑难疾病中西医协作临床试点项目

Source(s) of funding:

Pilot Project of Clinical Collaboration of Traditional Chinese Medicine and Western Medicine for Major Difficult Diseases

研究疾病:

不孕症

研究疾病代码:

Target disease:

Infertility

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:

其它

Others

研究目的:

评价接受体外受精-胚胎移植治疗的不孕女性,使用麒麟丸对妊娠结局的影响。

Objectives of Study:

To assess the efficacies of Qilin Pill on pregnancy outcomes in infertile women undergoing IVF-ET treatment.

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. 愿意接受口服中药治疗并签署知情同意书的患者; 2. 符合本病西医诊断标准者及国家卫计委体外受精-胚胎移植技术适应症; 3. 符合中医不孕症肝郁肾虚辨证标准; 4. 年龄25~42岁; 5. 基础FSH≤ 10 IU/L; 6. AFC≥8个; 7. 中国公民; 8. 采用体外受精-胚胎移植技术助孕者(长方案及超常方案)。

Inclusion criteria

1. Patients who are willing to take oral medications of traditional Chinese medicine (TCM) and sign the informed consent form; 2. In line with both the western diagnostic criteria and indications of IVF-ET set by National Health Commission of the People's Republic of China; 3. Infertility with liver-stagnation and kidney-deficiency according to TCM syndrome differentiation standard; 4. Aged 25 to 42; 5. Basal follicle stimulating hormone (bFSH) <=10 IU/L; 6. Antral follicle count (AFC) >= 8; 7. Chinese citizens; 8. Assisted reproduction with IVF-ET (long protocol or ultra-long protocol).

排除标准:

1. 子宫腺肌病、子宫肌瘤压迫宫腔线; 2. 未处理的输卵管积水; 3. 未治愈子宫内膜疾病; 4. 冻胚移植的女性; 5. 入组前3个月使用治疗不孕症相关中药的患者; 6. 正参加或一个月内参加了其他中药临床试验的患者; 7. 有辅助生殖技术禁忌症者; 8. 存在严重生殖道解剖异常者; 9. 反复种植失败者(经历3次及以上移植周期,且累积移植至少4枚卵裂期优质胚胎或3枚优质囊胚而未获得临床妊娠)。

Exclusion criteria:

1. Adenomyosis or uterine fibroids compressing the uterine cavity line; 2. Untreated hydrosalpinx; 3. Endometrial diseases being not cured; 4. Frozen embryo transplantation; 5. Treatment of TCM for infertility within 3 months; 6. Patients who are participating or have participated in other clinical trials of TCM within one month; 7. Contraindications to assisted reproductive technology; 8. Severe anatomical abnormalities of the reproductive tract; 9. Repeated implantation failure (RIF, failure to clinical pregnancy after transfer in three or more IVF treatment cycles, with cumulative transfer of at least four cleavage-stage high-quality embryos or three high-quality blastocysts).

研究实施时间:

Study execute time:

From 2019-11-01

To      2020-06-30

征募观察对象时间:

Recruiting time:

From 2019-11-01

To      2020-06-30

干预措施:

Interventions:

组别:

长方案安慰剂组

样本量:

378

Group:

Placebo Group with long protocol

Sample size:

干预措施:

服用安慰剂

干预措施代码:

Intervention:

taking placebo

Intervention code:

组别:

长方案试验组

样本量:

378

Group:

Qilin Pill Group with long protocol

Sample size:

干预措施:

服用麒麟丸

干预措施代码:

Intervention:

taking Qilin Pill

Intervention code:

组别:

超长方案试验组

样本量:

378

Group:

Qilin Pill Group with ultra-long protocol

Sample size:

干预措施:

服用麒麟丸

干预措施代码:

Intervention:

taking Qilin Pill

Intervention code:

组别:

超长方案安慰剂组

样本量:

378

Group:

Placebo Group with ultra-long protocol

Sample size:

干预措施:

服用安慰剂

干预措施代码:

Intervention:

taking Qilin Pill

Intervention code:

样本总量 Total sample size : 1512

研究实施地点:

Countries of recruitment
and research settings:

国家:

中国

省(直辖市):

陕西省

市(区县):

西安

Country:

China

Province:

Shannxi

City:

Xi'an

单位(医院):

西北妇女儿童医院

单位级别:

三级甲等

Institution/hospital:

Northwest Women and Children's Hospital

Level of the institution:

Tertiary A

测量指标:

Outcomes:

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:

指标中文名:

活产率

指标类型:

主要指标

Outcome:

live birth 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:

正在进行

Recruiting

年龄范围:

最小 25
Min age years
最大 42
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):

该试验设计为随机、双盲、安慰剂对照临床试验,通过计算机程序以1:1的比例按照长方案和超常方案被随机分配为两层。每层内按照1:1比例随机分配为麒麟丸试验组和安慰剂组(由药厂制作外表与真正药物相同的药丸)。

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

In this randomized, double-blind, placebo-controlled clinical trial, randomization was completed by a research assistant not otherwise involved in the study: a table of numbers representing long protocol and ultra-long protocol was randomized (1:1) by a computer program.

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):

不公开

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

private

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:

西北妇女儿童医院生殖医学中心内部数据库及病例报告表

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

Case Report Form and Data base of Reproduction Center of the Northwest Women and Children's Hospital

数据管理委员会:

Data Managemen Committee:

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):

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