ChiCTR2000033918 版本V1.3 版本创建时间2020/06/16 19:05:30 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:

ChiCTR2000033918 

最近更新日期:

Date of Last Refreshed on:

2020-06-16 19:02:53 

注册时间:

Date of Registration:

2020-06-16 00:00:00 

注册号状态:

补注册

Registration Status:

Retrospective registration

注册题目:

机器人辅助 Oxford 单髁膝关节置换术 (UKA) 中部件定位优于传统技术:一项 5 年随访研究

Public title:

Superior component position during robotic-assisted Oxford unicompartmental knee arthroplasty (UKA) compared with conventional technique: a 5-year follow-up study

注册题目简写:

English Acronym:

研究课题的正式科学名称:

机器人辅助 Oxford 单髁膝关节置换术 (UKA) 中部件定位优于传统技术:一项 5 年随访研究

Scientific title:

Superior component position during robotic-assisted Oxford unicompartmental knee arthroplasty (UKA) compared with conventional technique: a 5-year follow-up 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:

张震祥 

研究负责人:

张震祥 

Applicant:

Zhenxiang Zhang 

Study leader:

Zhenxiang Zhang 

申请注册联系人电话:

Applicant telephone:

+86 21 86532798

研究负责人电话:

Study leader's telephone:

+86 21 86532798

申请注册联系人传真 :

Applicant Fax:

+86 21 86532798

研究负责人传真:

Study leader's fax:

+86 21 86532798

申请注册联系人电子邮件:

Applicant E-mail:

Zhenxiangzhang1982@126.com

研究负责人电子邮件:

Study leader's E-mail:

Zhenxiangzhang1982@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:

江苏省泰州市海陵区太湖路366号

研究负责人通讯地址:

江苏省泰州市海陵区太湖路366号

Applicant address:

366 Taihu Road, Hailing District, Taizhou, Jiangsu

Study leader's address:

366 Taihu Road, Hailing District, Taizhou, Jiangsu

申请注册联系人邮政编码:

Applicant postcode:

225300

研究负责人邮政编码:

Study leader's postcode:

225300

申请人所在单位:

江苏省泰州市人民医院骨科

Applicant's institution:

Orthopedic Department, Taizhou People's Hospital

研究负责人所在单位:

江苏省泰州市人民医院骨科

Affiliation of the Leader:

Orthopedic Department, Taizhou People's Hospital

是否获伦理委员会批准:

否/No

Approved by ethic committee:

No

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:

江苏省泰州市人民医院

Primary sponsor:

Taizhou People's Hospital

研究实施负责(组长)单位地址:

江苏省泰州市海陵区太湖路366号

Primary sponsor's address:

366 Taihu Road, Hailing District, Taizhou, Jiangsu

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):

泰州

Country:

China

Province:

Jiangsu

City:

Taizhou

单位(医院):

泰州市人民医院

具体地址:

海陵区太湖路366号

Institution
hospital:

Taizhou People's Hospital

Address:

366 Taihu Road, Hailing District

经费或物资来源:

自费

Source(s) of funding:

self-raised

Target disease:

Unicompartmental knee arthroplasty

Target disease code:

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

探索性研究/预试验 

Study phase:

0

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

机器人辅助 Oxford 单髁膝关节置换术 (UKA) 中部件定位优于传统技术:一项 5 年随访研究。  

Objectives of Study:

Superior component position during robotic-assisted Oxford unicompartmental knee arthroplasty (UKA) compared with conventional technique: A 5-year follow-up 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:

(1) 年龄 45-75 岁;(2) ASA 分级 Ⅰ-Ⅲ 级;(3) 术前活动正常;(4) 股-髌间室 Ⅲ 级以下、外侧间室 Ⅳ 级以下关节炎改变;(5) BMI≤30,内翻小于 10°

Inclusion criteria

(1) 45-75 years old; (2) the evaluated ASA physical status between I-III; (3) with normal mobilization before operations; (4) the changes of arthritis below grade III in the femoral-patella compartment and below grade IV in the lateral compartment; (5) BMI ≤ 30 and the varus degree less than 10°.

排除标准:

韧带功能不全;损伤相关关节炎;畸形加重;神经运动障碍;对侧膝关节、髋关节、足部或踝关节病理状态导致明显步态改变或疼痛;最终需要 TKA 的患者。

Exclusion criteria:

insuf?ciency of ligament; in?ammation-related arthritis; augmentation for the deformity; disorders in neurological movement; pathological status of the contralateral knee, hips, feet, or ankles resulting in obvious gait alteration or pain; those eventually requiring a TKA.

研究实施时间:

Study execute time:

From 2010-01-01 00:00:00 To 2020-01-01 00:00:00  

征募观察对象时间:

Recruiting time:

From 2010-01-01 00:00:00 To 2015-01-01 00:00:00  

干预措施:

Interventions:

组别:

ROA组vs传统技术组

样本量:

85

Group:

ROA group vs COA group

Sample size:

干预措施:

机器人辅助手术 vs 传统技术

干预措施代码:

Intervention:

Robotic-assisted surgery vs conventional technique

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):

泰州 

Country:

China 

Province:

Jiangsu 

City:

Taizhou 

单位(医院):

泰州市人民医院 

单位级别:

三级甲等 

Institution
hospital:

Taizhou People's Hospital

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

KSP 功能量表

指标类型:

主要指标

Outcome:

KSP scores

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

KSF功能量表

指标类型:

主要指标

Outcome:

KSF scores

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

KSC功能量表

指标类型:

主要指标

Outcome:

KSC scores

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:

结束

/Completed

年龄范围:

Participant age:

最小 Min age years
最大 Max age years

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):

根据计算机生成的程序对参与者进行随机分组。随机化代码由独立研究者保存,以确保盲态。在收集知情同意书和获得基线测量值后,将受试者随机分配到机器人辅助或传统 UKA 组。根据应用的技术采用分层随机化。

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

Participants have been randomized according to a computer-generated procedure. The randomization codes have been kept by an independent researcher ensuring blindness. The subjects have been randomly assigned into robotic-assisted or conventional UKA groups following collection of informed consent and acquisition of baseline measur

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

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):

-

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

-

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:

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

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

Data collection and management consists of two parts, one is case record form and the other is electronic collection and management system

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2020-06-16 18:59:01