|
审核状态: Project audit state: |
通过审核 Successful |
|
注册号: Registration number: |
ChiCTR2100048582 |
|
最近更新日期: Date of Last Refreshed on: |
2021-07-11 04:31:34 |
|
注册时间: Date of Registration: |
2021-07-11 00:00:00 |
|
注册号状态: |
预注册 |
|
Registration Status: |
Prospective registration |
|
注册题目: |
心功能分级和心脏舒张功能分级对麻醉手术风险预测的差异性--前瞻性队列研究 |
|
Public title: |
Performance Differences between NYHA Functional Classification and Diastolic Dysfunction Grade in Perioperative Risk Prediction: a prospective cohort study |
|
注册题目简写: |
心功能分级和心脏舒张功能分级与麻醉手术风险 |
|
English Acronym: |
Cardiac function grade and diastolic function grade and the risk of anesthesia surgery |
|
研究课题的正式科学名称: |
心功能分级和心脏舒张功能分级对麻醉手术风险预测的差异性--前瞻性队列研究 |
|
Scientific title: |
Performance Differences between NYHA Functional Classification and Diastolic Dysfunction Grade in Perioperative Risk Prediction: a prospective cohort 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: |
金小高 |
研究负责人: |
金小高 |
|
Applicant: |
Xiaogao Jin |
Study leader: |
Xiaogao Jin |
|
申请注册联系人电话: Applicant telephone: |
18378344400 |
研究负责人电话: Study leader's telephone: |
18378344400 |
|
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: |
jinxiaogao@yeah.net |
研究负责人电子邮件: Study leader's E-mail: |
jinxiaogao@yeah.net |
|
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: |
郑州大学附属郑州中心医院麻醉与围术期医学科 |
研究负责人通讯地址: |
郑州大学附属郑州中心医院麻醉与围术期医学科 |
|
Applicant address: |
Zhengzhou Central Hospital affiliated to Zhengzhou University |
Study leader's address: |
Zhengzhou Central Hospital affiliated to Zhengzhou University |
|
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: |
郑州大学附属郑州中心医院 |
||
|
Applicant's institution: |
Zhengzhou Central Hospital Affiliated to Zhengzhou University |
||
|
研究负责人所在单位: |
郑州大学附属郑州中心医院 |
||
|
Affiliation of the Leader: |
|
||
|
是否获伦理委员会批准: |
是/Yes |
||
|
Approved by ethic committee: |
Yes |
||
|
伦理委员会批件文号: Approved No. of ethic committee: |
202143 |
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: |
郑州市中心医院医学伦理委员会 |
||
|
Name of the ethic committee: |
The Ethics Committee of Zhengzhou Central Hospital |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2021-07-02 00:00:00 |
||
|
伦理委员会联系人: |
刘瑞华 |
||
|
Contact Name of the ethic committee: |
Ruihua Liu |
||
|
伦理委员会联系地址: |
郑州大学附属郑州中心医院 |
||
|
Contact Address of the ethic committee: |
Zhengzhou Central Hospital Affiliated to Zhengzhou University |
||
|
伦理委员会联系人电话: Contact phone of the ethic committee: |
0371-61172993 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
zbdywk@126.com |
|
研究实施负责(组长)单位: |
郑州大学附属郑州中心医院 |
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
Primary sponsor: |
Zhengzhou Central Hospital Affiliated to Zhengzhou University, Zhengzhou, 450007, China |
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
河南省郑州大学附属郑州中心医院 |
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
Primary sponsor's address: |
Zhengzhou Central Hospital Affiliated to Zhengzhou University, Zhengzhou, 450007, China |
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
经费或物资来源: |
无 |
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
Source(s) of funding: |
None |
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
Target disease: |
heart disease |
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
Target disease code: |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
研究类型: |
观察性研究 |
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
Study type: |
Observational study |
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
研究所处阶段: |
探索性研究/预试验 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
Study phase: |
0 |
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
研究设计: |
诊断性病例对照试验 |
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
Study design: |
Diagnostic test: case-control |
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
研究目的: |
比较心功能分级和心脏舒张功能分级对预测心脏射血分数正常但舒张功能不全患者麻醉结果的可靠性---前瞻性队列研究 |
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
Objectives of Study: |
Performance Differences between NYHA Functional Classification and Diastolic Dysfunction Grade in Perioperative Risk Prediction: a prospective cohort study |
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
药物成份或治疗方案详述: |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
Description for medicine or protocol of treatment in detail: |
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
纳入标准: |
2021年07月15日-2021年10月15日在上述三家医院进行择期手术的且有心脏超声检查的大于18岁患者。 |
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
Inclusion criteria |
All patients with Echo-cardiogram examination who underwent elective surgery in the above three hospitals from July 15, 2021 to October 15, 2021. |
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
排除标准: |
1.EF值大于50% |
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
Exclusion criteria: |
1.EF value greater than 50% |
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2021-07-15 00:00:00至 To 2021-10-15 00:00:00 |
征募观察对象时间: Recruiting time: |
从From 2021-07-15 00:00:00 至 To 2021-10-15 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: |
男女均可 |
Gender: |
Both |
||||||
|
随机方法(请说明由何人用什么方法产生随机序列): |
预试验,没有随机方法 |
||||||||
|
Randomization Procedure (please state who generates the random number sequence and by what method): |
None 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: |
None |
|
Blinding: |
None |
|
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 |
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): |
在对原始数据进行整理后,上传数据到中国临床试验中心,实现共享。2021年11月20日-2022年02月20日: 公开并上传所有数据 |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
The clinical trial plan to release all data through Chinese clinical trial registry between November 20, 2021 and February 20, 2021. The public data should be arranged and approved before release. |
|
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 Record Form, CRF |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |