ChiCTR-TRC-10000983 版本V1.0 版本创建时间2015/06/17 23:21:46 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:

ChiCTR-TRC-10000983 

最近更新日期:

Date of Last Refreshed on:

2015-05-04 11:56:07 

注册时间:

Date of Registration:

2010-07-17 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

改良子宫切口在前置胎盘患者剖宫产术中临床应用评估研究方案

Public title:

clinical application of improved uterus incision in placenta previa cesarean section

注册题目简写:

English Acronym:

研究课题的正式科学名称:

改良子宫切口在前置胎盘患者剖宫产术中临床应用评估研究方案

Scientific title:

Randomized controlled clinical trials of improved uterus incision in placenta previa cesarean section in comparison with tradition incision

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:

颜婷 

研究负责人:

邹丽 

Applicant:

Yan Ting 

Study leader:

Zou Li 

申请注册联系人电话:

Applicant telephone:

+86 13477033419

研究负责人电话:

Study leader's
telephone:

+86 027 85351639

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:

276472670@qq.com

研究负责人电子邮件:

Study leader's E-mail:

medzouli@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:

中国武汉协和医院产科

研究负责人通讯地址:

中国武汉协和医院产科

Applicant address:

Obstetrics Department of Wuhan Union Hospital, Wuhan province, China

Study leader's address:

Obstetrics Department of Wuhan Union Hospital, Wuhan province, China

申请注册联系人邮政编码:

Applicant postcode:

430000

研究负责人邮政编码:

Study leader's postcode:

430000

申请人所在单位:

华中科技大学附属协和医院产科

Applicant's institution:

Obstetrics Department of Wuhan Union Hospital, Wuhan province, China

研究负责人所在单位:

Affiliation of the Leader:

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:

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:

2013-08-26 00:00:00

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:

华中科技大学附属协和医院产科

Primary sponsor:

Obstetrics Department of Wuhan Union Hospital, Wuhan province, China

研究实施负责(组长)单位地址:

湖北武汉解放大道1277

Primary sponsor's address:

Obstetrics Department of Wuhan Union Hospital, Wuhan province, China

试验主办单位(项目批准或申办者):

Secondary sponsor:

经费或物资来源:

协和医院院内项目

Source(s) of funding:

Subject Funding of Wuhan Union Hospital

研究疾病:

前置胎盘  

Target disease:

placenta previa

研究疾病代码:

O03

Target disease code:

O03

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

I期临床试验 

Study phase:

1

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

以传统子宫下段横切口为对照评价改良子宫切口在前置胎 盘患者剖宫产术应用的有效性和安全性  

Objectives of Study:

Evaluate the safety and effectiveness of improved incision in comparison with tradition incision

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.符合前置胎盘诊断标准且B超结果显示子宫前壁下段有胎盘附着或胎位异常者。
2.育龄妇女
3.肝肾功能无明显异常(ALT、AST、Cr超过正常上限1.5倍以上)
4.既往无严重的心、肝、肾等重要脏器严重器质性疾病及糖尿病、结核等疾病病史
5.自愿作为受试对象并已签署知情同意

Inclusion criteria

1.Meet the diagnostic criteria of placenta previa,and placenta previa adhere to lower segment of anterior uterine in B ultrasound;2.Women of childbearing age;3.without serious liver and kidney dysfunction (ALT, AST, Cr, higher than 1.5 times of upper limit of normal);4.without serious organic diseases of vital organs (such as heart, liver, kidney) or diabetes TB in previous history;5.Sign the informed consent voluntarily.

排除标准:

1.不符合前置胎盘诊断标准
2.既往有严重器质性病变病史
3.发热
4.严重感染
5.病人有自身免疫性疾病
6. 观察医师认为的其它不符合入选的情况

Exclusion criteria:

1.do not meet the diagnostic criteria of placenta previa;
2.with serious organic diseases of vital organs in previous history;
3.fever;
4.serious infection;
5.with autoimmune disease;
6.other situations that doctors consider should exclude.

研究实施时间:

Study execute time:

From 2010-01-01 00:00:00 To 2012-01-01 00:00:00  

征募观察对象时间:

Recruiting time:

From 2010-01-01 00:00:00 To 2012-01-01 00:00:00

干预措施:

Interventions:

组别:

1

样本量:

55

Group:

1

Sample size:

干预措施:

传统手术切口

干预措施代码:

Intervention:

traditional Incision

Intervention code:

组别:

2

样本量:

65

Group:

2

Sample size:

干预措施:

改良子宫切口(L或J型)

干预措施代码:

Intervention:

improved incision

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

湖北 

市(区县):

武汉 

Country:

China

Province:

Hubei

City:

Wuhan

单位(医院):

武汉协和医院 

单位级别:

三甲医院 

Institution
hospital:

Wuhan Union Hospital

Level of the institution:

Tertiary A hospital

测量指标:

Outcomes:

指标中文名:

术后首次下床活动时间

指标类型:

主要指标

Outcome:

volume of bleeding in surgery

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

术后排气时间

指标类型:

主要指标

Outcome:

time of fetus parturition

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

术中出血量

指标类型:

次要指标

Outcome:

The first time getting out of bed after surgery

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

术中输血量

指标类型:

次要指标

Outcome:

the first time farting after surgery

Type:

Secondary 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Apgar评分

指标类型:

次要指标

Outcome:

volume of blood transfusion

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

胎儿娩出时间

指标类型:

次要指标

Outcome:

Apgar Score

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

并发症发生率

指标类型:

次要指标

Outcome:

Incidence of complication

Type:

Secondary 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:

正在进行

Recruiting

年龄范围:

Participant age:

最小 Min age years
最大 Max age 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):

随机数字表

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

随机数字表

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:

临床医生 否 数据采集人员 是 患者 否 研究设计者 否 统计分析人员 是

Blinding:

data analysis staff: yes data collection staff: yes trial organizer: no doctors: no patients: no

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

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):

武汉协和医院产科

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

Obstetrics Department of Wuhan Union Hospital, Wuhan province, China

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:

武汉协和医院产科

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

Obstetrics Department of Wuhan Union Hospital, Wuhan province, China

数据与安全监察委员会:

Data and Safety Monitoring Committee:

注册人:

Name of Registration:

 2010-09-23 00:00:00