ChiCTR2000035286 版本V1.2 版本创建时间2020/08/07 23:32:43 中国临床试验注册中心

审核状态:

Project audit state:

通过审核

Successful

注册号:

Registration number:

ChiCTR2000035286 

最近更新日期:

Date of Last Refreshed on:

2020-08-07 23:30:49 

注册时间:

Date of Registration:

2020-08-06 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

前置胎盘严重产后出血临床高危因素分析

Public title:

Analysis of clinical high-risk factors for severe postpartum hemorrhage of placenta previa

注册题目简写:

English Acronym:

研究课题的正式科学名称:

前置胎盘严重产后出血临床高危因素分析

Scientific title:

Analysis of clinical high-risk factors for severe postpartum hemorrhage of placenta previa

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:

姜子燕 

研究负责人:

葛志平 

Applicant:

Jiang ziyan 

Study leader:

Ge Zhiping 

申请注册联系人电话:

Applicant telephone:

+86 13512534017

研究负责人电话:

Study leader's
telephone:

+86 13851528816

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:

zyjiangchm@163.com

研究负责人电子邮件:

Study leader's E-mail:

gzp88142@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:

南京市广州路300号

研究负责人通讯地址:

南京市广州路300号

Applicant address:

300 Guangzhou Road, Nanjing, Jiangsu, China

Study leader's address:

300 Guangzhou Road, Nanjing, Jiangsu, China

申请注册联系人邮政编码:

Applicant postcode:

210029

研究负责人邮政编码:

Study leader's postcode:

210029

申请人所在单位:

南京医科大学第一附属医院/江苏省人民医院

Applicant's institution:

The First Affiliated Hospital of Nanjing Medical University

研究负责人所在单位:

南京医科大学第一附属医院/江苏省人民医院

Affiliation of the Leader:

The First Affiliated Hospital of Nanjing 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:

2020-SR-256

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:

南京医科大学第一附属医院伦理委员会

Name of the ethic committee:

Ethics Committee of the First Affiliated Hospital of Nanjing Medical University

伦理委员会批准日期:

Date of approved by ethic committee:

2020-07-15 00:00:00

伦理委员会联系人:

张馥敏

Contact Name of the ethic committee:

Zhang Fumin

伦理委员会联系地址:

南京市广州路300号

Contact Address of the ethic committee:

南京医科大学第一附属医院/江苏省人民医院

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 025-68306360

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:

南京医科大学第一附属医院/江苏省人民医院

Primary sponsor:

First Affiliated Hospital of Nanjing Medical University

研究实施负责(组长)单位地址:

南京市广州路300号

Primary sponsor's address:

300 guangzhou Road

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

江苏

市(区县):

南京

Country:

China

Province:

Jiangsu

City:

Nanjing

单位(医院):

南京医科大学第一附属医院

具体地址:

广州路300号

Institution
hospital:

The First Affiliated Hospital of Nanjing Medical University

Address:

300 Guangzhou Road

经费或物资来源:

国家自然科学基金面上项目

Source(s) of funding:

National Natural Science Foundation of China (81971407)

研究疾病:

胎盘植入  

Target disease:

Placenta Accreta Spectrum

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:

横断面 

Study design:

Cross-sectional 

研究目的:

通过回顾性研究前置胎盘严重产后出血(>2000mL)的临床危险因素,推导出前置胎盘患者严重产后出血方程,建立风险评估系统。  

Objectives of Study:

Through retrospective research on the clinical risk factors of severe postpartum hemorrhage (> 2000mL) in the placenta previa patients. To build the equation of severe postpartum hemorrhage in patients and help establish the scoring system for the risk assessment.

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

在我院产科分娩的前置胎盘孕妇。

Inclusion criteria

all the patients of placenta previa

排除标准:

高血压、心脏病、血液系统疾病等妊娠并发症及合并症。

Exclusion criteria:

Pregnancy complications and complications such as hypertension, heart disease, and blood system diseases.

研究实施时间:

Study execute time:

From 2012-10-01 00:00:00 To 2020-07-30 00:00:00  

征募观察对象时间:

Recruiting time:

From 2020-08-04 00:00:00 To 2020-12-31 00:00:00

干预措施:

Interventions:

组别:

case series

样本量:

500

Group:

case series

Sample size:

干预措施:

干预措施代码:

Intervention:

Nil

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

江苏 

市(区县):

南京 

Country:

China

Province:

Jiangsu

City:

Nanjing

单位(医院):

南京医科大学第一附属医院 

单位级别:

三甲 

Institution
hospital:

The First Affiliated Hospital of Nanjing Medical University

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

产后出血量

指标类型:

主要指标

Outcome:

volume of blood loss

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

孕妇一般临床特征

指标类型:

次要指标

Outcome:

clinical characteristics

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

子宫切除率

指标类型:

主要指标

Outcome:

rate of hysterectomy

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

ICU收住率

指标类型:

主要指标

Outcome:

ICU admission

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

新生儿窒息率

指标类型:

主要指标

Outcome:

Neonatal asphyxia 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:

组织:

Sample Name:

N/A

Tissue:

人体标本去向

其它  

说明

Fate of sample:

0thers  

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 18 years
最大 Max age 45 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):

N/A

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

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):

论文支持材料

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

supportive material from artical

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:

病例记录表

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

case report form

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2020-08-06 23:10:54