静脉复合麻醉用于取卵术对妊娠结局的影响:一项回顾性研究

注册号:

Registration number:

ChiCTR2200058833 

最近更新日期:

Date of Last Refreshed on:

2022-12-30 10:21:39 

注册时间:

Date of Registration:

2022-04-17 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

静脉复合麻醉用于取卵术对妊娠结局的影响:一项回顾性研究

Public title:

Effect of intravenous combined anesthesia on pregnancy outcome during oocyte retrieval: a retrospective study

注册题目简写:

English Acronym:

研究课题的正式科学名称:

静脉复合麻醉用于取卵术对妊娠结局的影响:一项回顾性研究

Scientific title:

Effect of intravenous combined anesthesia on pregnancy outcome during oocyte retrieval: a retrospective study

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:

鲁显福 

研究负责人:

鲁显福 

Applicant:

Xian-Fu Lu 

Study leader:

Xian-Fu Lu 

申请注册联系人电话:

Applicant telephone:

+86 18256031820

研究负责人电话:

Study leader's
telephone:

+86 18256031820

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:

lxf0001@126.com

研究负责人电子邮件:

Study leader's E-mail:

lxf0001@126.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:

安徽省合肥市蜀山区绩溪路218号

研究负责人通讯地址:

安徽省合肥市蜀山区绩溪路218号

Applicant address:

218 Jixi Road, Shushan District, Hefei, Anhui

Study leader's address:

218 Jixi Road, Shushan District, Hefei, Anhui, 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:

安徽医科大学第一附属医院

Applicant's institution:

First Affiliated Hospital of Anhui Medical University

研究负责人所在单位:

安徽医科大学第一附属医院

Affiliation of the Leader:

First Affiliated Hospital of Anhui Medical University

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:

PJ2022-02-39

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:

安徽医科大学第一附属医院临床医学研究伦理委员会

Name of the ethic committee:

Ethics Committee of Clinical Medical Research, the First Affiliated Hospital of Anhui Medical University

伦理委员会批准日期:

Date of approved by ethic committee:

2022-02-17 00:00:00

伦理委员会联系人:

周涛

Contact Name of the ethic committee:

Tao Zhou

伦理委员会联系地址:

安徽省合肥市蜀山区绩溪路218号安徽医科大学第一附属医院行政楼6F

Contact Address of the ethic committee:

6F, Administration Building, The First Affiliated Hospital of Anhui Medical University, 218 Jixi Road, Shushan District, Hefei, Anhui

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 0551-62923537

伦理委员会联系人邮箱:

Contact email of the ethic committee:

331417268@qq.com

研究实施负责(组长)单位:

安徽医科大学第一附属医院

Primary sponsor:

The First Affiliated Hospital of Anhui Medical University

研究实施负责(组长)单位地址:

安徽省合肥市蜀山区绩溪路218号

Primary sponsor's address:

218 Jixi Road, Shushan District, Hefei, Anhui

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

安徽

市(区县):

合肥

Country:

China

Province:

Anhui

City:

Hefei

单位(医院):

安徽医科大学第一附属医院

具体地址:

安徽省合肥市蜀山区绩溪路218号

Institution
hospital:

First Affiliated Hospital of Anhui Medical University

Address:

218 Jixi Road, Shushan District

经费或物资来源:

安徽医科大学第一附属医院院长基金

Source(s) of funding:

Dean's Fund of the First Affiliated Hospital of Anhui Medical University

研究疾病:

不孕症  

Target disease:

Infertility

研究疾病代码:

Target disease code:

研究类型:

观察性研究

Study type:

Observational study

研究所处阶段:

回顾性研究 

Study phase:

Retrospective study

研究设计:

病例对照研究 

Study design:

Case-Control study 

研究目的:

不同静脉用药方案在无痛取卵术中的应用对辅助生殖助孕结局的影响  

Objectives of Study:

The influence of the application of different intravenous medications in painless egg retrieval on the outcome of assisted reproduction

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. 接受植入前基因诊断(PGD)或植入前基因筛选(PGS)患者;
2. 正在参加其他临床研究者。

Exclusion criteria:

1. Patients receiving the preimplantation genetic diagnosis (PGD) or preimplantation genetic screening (PGS);
2. Those who are participating in other clinical research.

研究实施时间:

Study execute time:

From 2021-06-01 00:00:00 To 2024-06-30 00:00:00  

征募观察对象时间:

Recruiting time:

From 2022-06-01 00:00:00 To 2024-06-30 00:00:00

干预措施:

Interventions:

组别:

对照组

样本量:

500

Group:

Control group

Sample size:

干预措施:

哌替啶 50 mg

干预措施代码:

Intervention:

Meperidine 50 mg

Intervention code:

组别:

A组

样本量:

500

Group:

Group A

Sample size:

干预措施:

依托咪酯+丙泊酚

干预措施代码:

Intervention:

Etomidate + Propofol

Intervention code:

组别:

B组

样本量:

500

Group:

Group B

Sample size:

干预措施:

依托咪酯+瑞芬太尼

干预措施代码:

Intervention:

Etomidate + Remifentanil

Intervention code:

组别:

C组

样本量:

500

Group:

Group C

Sample size:

干预措施:

依托咪酯+丙泊酚+瑞芬太尼

干预措施代码:

Intervention:

Etomidate + Propofol + Remifentanil

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

安徽 

市(区县):

合肥 

Country:

China

Province:

Anhui

City:

Hefei

单位(医院):

安徽医科大学第一附属医院 

单位级别:

三甲 

Institution
hospital:

First Affiliated Hospital of Anhui Medical University

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

IVF/ICSI 周期结局

指标类型:

主要指标

Outcome:

IVF/ICSI cycle outcome

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

妊娠结局

指标类型:

主要指标

Outcome:

Pregnancy outcome

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

手术时间、麻醉药物和剂量

指标类型:

附加指标

Outcome:

Operation time, anesthetic drugs and dosage

Type:

Additional indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

麻醉不良反应

指标类型:

附加指标

Outcome:

Adverse reactions to anesthesia

Type:

Additional 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:

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 40 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):

收集 2018年1月至2021年1月在安徽医科大学附属第一医院生殖医学中心进行 体外授精、卵母细胞浆内单精子注射技术辅助生殖技术助孕的患者,治疗周期的临床及实验室资料。 根据患者的麻醉方式分为无静脉麻醉组(对照组)、丙泊酚+依托咪酯组(A组)、依托咪酯+瑞芬组(B组)、依托咪酯+丙泊酚+瑞分组(C组)。

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

We will collect patients who underwent in vitro fertilization and intracytoplasmic sperm injection technology assisted reproductive technology in the Reproductive Medicine Center of the First Affiliated Hospital of Anhui Medical University from January 2018 to January 2021, and the clinical and experimental treatment cycle

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:

Blinding:

试验完成后的统计结果(上传文件):

Calculated Results after
the Study Completed(upload file):

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):

试验完成后可以给主要负责人发邮件索取原始数据

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

After the test is completed, you can email the main person in charge to request the original 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(CRF表, Version 1.0)

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

Case Report Form (CRF Form, Version 1.0)

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2022-04-17 21:07:13