|
注册号: Registration number: |
ChiCTR2100049841 |
|
最近更新日期: Date of Last Refreshed on: |
2022-04-16 06:42:23 |
|
注册时间: Date of Registration: |
2021-08-10 00:00:00 |
|
注册号状态: |
预注册 |
|
Registration Status: |
Prospective registration |
|
注册题目: |
基于子宫内膜容受性检测的个体化胚胎移植对 PGT 患者妊娠结局的影响:多中心、 随机、对照、开放标签的临床试验 |
|
Public title: |
Effect of individualized embryo transfer based on endometrial receptivity test on clinical outcome of embryo implantation in patients with Preimplantation Genetic Testing: a multicenter, randomized, controlled, open-label clinical trial |
|
注册题目简写: |
|
|
English Acronym: |
|
|
研究课题的正式科学名称: |
基于子宫内膜容受性检测的个体化胚胎移植对 PGT 患者妊娠结局的影响:多中心、 随机、对照、开放标签的临床试验 |
|
Scientific title: |
Effect of individualized embryo transfer based on endometrial receptivity test on clinical outcome of embryo implantation in patients with Preimplantation Genetic Testing: a multicenter, randomized, controlled, open-label clinical trial |
|
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: |
干润新 |
研究负责人: |
李艳萍 |
|
Applicant: |
Gan Runxin |
Study leader: |
Li Yanping |
|
申请注册联系人电话: Applicant telephone: |
+86 18508422003 |
研究负责人电话:
Study leader's |
+86 13607317798 |
|
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: |
grxhehe@126.com |
研究负责人电子邮件: Study leader's E-mail: |
liyanp@csu.edu.cn |
|
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: |
中国湖南省长沙市开福区湘雅路87号 |
研究负责人通讯地址: |
中国湖南省长沙市开福区湘雅路87号 |
|
Applicant address: |
87 Xiangya Road, Kaifu District, Changsha, Hunan, China |
Study leader's address: |
87 Xiangya Road, Kaifu District, Changsha, Hunan, 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: |
中南大学湘雅医院 |
||
|
Applicant's institution: |
Xiangya Hospital, Central South University |
||
|
研究负责人所在单位: |
中南大学湘雅医院 |
||
|
Affiliation of the Leader: |
Xiangya Hospital, Central South University |
||
|
是否获伦理委员会批准: |
是 |
||
|
Approved by ethic committee: |
Yes |
||
|
伦理委员会批件文号: Approved No. of ethic committee: |
科202201036 |
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: |
中南大学湘雅医院生殖医学伦理委员会 |
||
|
Name of the ethic committee: |
Medical Ethics Committee of Xiangya Hospital Central South University |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2022-01-29 00:00:00 | ||
|
伦理委员会联系人: |
肖佩君 |
||
|
Contact Name of the ethic committee: |
Xiao Peijun |
||
|
伦理委员会联系地址: |
中国湖南省长沙市开福区湘雅路87号 |
||
|
Contact Address of the ethic committee: |
87 Xiangya Road, Kaifu District, Changsha, Hunan, China |
||
|
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: |
中南大学湘雅医院 |
||||||||||||||||||||||
|
Primary sponsor: |
Xiangya Hospital, Central South University |
||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
中国湖南省长沙市开福区湘雅路87号湘雅医院 |
||||||||||||||||||||||
|
Primary sponsor's address: |
87 Xiangya Road, Kaifu District, Changsha, Hunan, China |
||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||
|
经费或物资来源: |
亿康基因有限公司 |
||||||||||||||||||||||
|
Source(s) of funding: |
Yikon Genomics Ltd |
||||||||||||||||||||||
|
研究疾病: |
不孕症 |
||||||||||||||||||||||
|
Target disease: |
infertility |
||||||||||||||||||||||
|
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: |
随机平行对照 |
||||||||||||||||||||||
|
Study design: |
Parallel |
||||||||||||||||||||||
|
研究目的: |
主要目的: 1.通过一项多中心临床研究,比较根据ERT计算的时间进行胚胎移植与传统时间进行胚胎移植对于PGT 患者临床妊娠结局的影响,建立一种有效的辅助生殖技术胚胎移植策略; 2.调查WOI移位在不孕症人群中的发生率,解析WOI移位的高危因素。 |
||||||||||||||||||||||
|
Objectives of Study: |
Main purpose: 1. Through a multi-center clinical study, compare the effects of embryo transfer based on ERT calculation time and traditional time embryo transfer on clinical pregnancy outcomes of PGT patients, and establish an effective assisted reproductive technology embryo transfer strategy; 2. Investigate the incidence of WOI translocation in infertile population, and analyze the high-risk factors of WOI translocation. |
||||||||||||||||||||||
|
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.可能影响着床的子宫病变(包括宫腔粘连史、子宫内膜息肉、子宫内膜炎、子宫内膜结 核、子宫内膜增生、薄型子宫内膜、粘膜下肌瘤、子宫腺肌病),子宫畸形; |
||||||||||||||||||||||
|
Exclusion criteria: |
1. Uterine lesions that may affect implantation (including history of intrauterine adhesions, endometrial polyps, endometritis, endometrial tuberculosis, endometrial hyperplasia, thin endometrium, submucosal fibroids, adenomyosis ), uterine malformation; |
||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2021-08-01 00:00:00至 To 2023-08-31 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2022-03-01 00:00:00 至 To 2023-07-30 00:00:00 |
|
干预措施: Interventions: |
|
|
研究实施地点: Countries of recruitment and research settings: |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
测量指标: Outcomes: |
|
|
采集人体标本:
Collecting sample(s)
|
|
|
征募研究对象情况: Recruiting status: |
尚未开始 Not yet recruiting |
年龄范围: Participant age: |
|
||||||
|
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): |
分层区组随机(1:1):按照生殖医疗结构进行分层,再在各个生殖医疗结构内进行受试者的区组随机化 1:1进行随机分组。 |
||||||||
|
Randomization Procedure (please state who generates the random number sequence and by what method): |
stratified block randomization(1:1):Stratification was performed according to reproductive medical structures, and the patients were randomized in each reproductive medical structure with a 1:1 block randomization. |
||||||||
|
是否公开试验完成后的统计结果: Calculated Results after the Study Completed public access: |
公开/Public |
|
盲法: |
Not stated |
|
Blinding: |
Not stated |
|
试验完成后的统计结果(上传文件): |
|
|
Calculated Results after
|
|
|
是否共享原始数据: IPD sharing |
是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): |
研究结果发表后6个月,向研究者联系索取原始数据 |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
6 months after publication of results and Contact the researcher for raw data |
|
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: |
病例报告表及电子采集和管理系统 |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
Case Record Form and Electronic Data Capture |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |