ChiCTR2300077966 版本V1.1 版本创建时间2024/07/07 19:33:59 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:

ChiCTR2300077966 

最近更新日期:

Date of Last Refreshed on:

2023-11-24 16:16:52 

注册时间:

Date of Registration:

2023-11-24 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

针刺联合推拿治疗动眼神经麻痹的临床随机对照实验研究

Public title:

Effect of acupuncture combined with massage on oculomotor paralysis: a randomized clinical trial

注册题目简写:

English Acronym:

研究课题的正式科学名称:

针刺联合推拿治疗动眼神经麻痹的临床随机对照实验研究

Scientific title:

Effect of acupuncture combined with massage on oculomotor paralysis: a randomized clinical trial

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:

黄艳 

研究负责人:

黄艳 

Applicant:

Huang Yan 

Study leader:

Huang Yan 

申请注册联系人电话:

Applicant telephone:

+86 159 7009 4281

研究负责人电话:

Study leader's
telephone:

+86 159 7009 4281

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:

286322430@qq.com

研究负责人电子邮件:

Study leader's E-mail:

286322430@qq.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:

江西省赣州市章贡区西津路16号

研究负责人通讯地址:

江西省赣州市章贡区西津路16号

Applicant address:

No.16, Xijin Road, Zhanggong District, Ganzhou City, Jiangxi Province

Study leader's address:

No.16, Xijin Road, Zhanggong District, Ganzhou City, Jiangxi Province

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:

赣州市中医院

Applicant's institution:

Ganzhou Hospital of Traditional Chinese Medicine

研究负责人所在单位:

赣州市中医院

Affiliation of the Leader:

Ganzhou Hospital of Traditional Chinese Medicine

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:

GZSZYYKYLL20230095

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:

赣州市中医院医学伦理委员会

Name of the ethic committee:

Medical Ethics Committee of Ganzhou City Hospital of Traditional Chinese Medicine

伦理委员会批准日期:

Date of approved by ethic committee:

2023-11-03 00:00:00

伦理委员会联系人:

王磊

Contact Name of the ethic committee:

Wanglei

伦理委员会联系地址:

江西省赣州市章贡区西津路16号

Contact Address of the ethic committee:

No.16, Xijin Road, Zhanggong District, Ganzhou City, Jiangxi Province

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 797 801 9167

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:

赣州市中医院

Primary sponsor:

Ganzhou Hospital of Traditional Chinese Medicine

研究实施负责(组长)单位地址:

江西省赣州市章贡区西津路16号

Primary sponsor's address:

No.16, Xijin Road, Zhanggong District, Ganzhou City, Jiangxi Province

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

江西省

市(区县):

赣州市

Country:

China

Province:

Jiangxi Province

City:

Ganzhou City

单位(医院):

赣州市中医院

具体地址:

江西省赣州市章贡区西津路16号

Institution
hospital:

Ganzhou Hospital of Traditional Chinese Medicine

Address:

No.16, Xijin Road, Zhanggong District, Ganzhou City, Jiangxi Province

经费或物资来源:

赣州市中医院

Source(s) of funding:

Ganzhou Hospital of Traditional Chinese Medicine

研究疾病:

动眼神经麻痹  

Target disease:

oculomotor paralyses

研究疾病代码:

Target disease code:

研究类型:

干预性研究

Study type:

Interventional study

研究所处阶段:

II期临床试验 

Study phase:

2

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

本研究旨在通过临床随机对照试验 ,观察针刺联合推拿治疗动眼神经麻痹的临床疗效,从而为临床治疗动眼神经麻痹提供安全且有效的方法。  

Objectives of Study:

This study aims to observe the clinical efficacy of acupuncture combined with massage in the treatment of ooculomotor paralyses, thus providing a safe and effective method for the clinical treatment of oculomotor paralyses.

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

纳入标准:1、符合动眼神经麻痹症的诊断标准;2、年龄大于18岁小于75,性别不限;3、原发病病情控制稳定者;4签署知情同意书。

Inclusion criteria

1. Meet the diagnostic criteria of oculomotor paralyses; 2.To be aged 18 to 75 years old (both males and female patients are included) and 3. Primary disease with stable condition; 4 sign informed consent.

排除标准:

1)进行性眼外肌麻痹综合症(Shy-Gonatas综合症);先天性斜视、高度近视屈光不正者;做过眼科眼外肌手术斜视矫正术的患者 2)年龄小于18岁或大于75岁的患者 3)有严重心脏病或肝肾等疾病危及生命,以及意识不清者 4)严重感染者;眼局部感染者 5)妊娠期的妇女 6)精神病患者 7)患有传染性疾病患者 8)严重进展性疾病(如恶性肿瘤)或预后不良使患者极度衰竭的疾病 9)已知的出血倾向(止血或凝血功能障碍);目前正在使用治疗剂量的抗凝药,存在针刺后出血风险的患者 10)正在参加其它临床试验 11)拒绝签署知情同意书的患者

Exclusion criteria:

1. history of Shy-Gonatas syndrome, congenital strabismus,high myopia,extrocular muscle epithesis; 2. complications of severe systematic diseases such as cardiocerebrovascular disease, liver or kidney disease, or unconsciousness; 3. severe infection or infection around eyes; 4. pregnancy or lactation; 5. mental disease; 6. severe contagious disease; 7. serious progressive disease (malignant tumor) or poor prognosis caused multiple failure; 8. known bleeding tendency (Hemostatic Disorders or blood coagulation disorders); taken therapeutic dose anticoagulant drug caused bleeding risk after acupuncture; 9. participating other clinical trail; 10. refuse to sign the informed consent document.

研究实施时间:

Study execute time:

From 2023-12-01 00:00:00 To 2025-12-01 00:00:00  

征募观察对象时间:

Recruiting time:

From 2023-12-01 00:00:00 To 2024-06-01 00:00:00

干预措施:

Interventions:

组别:

联合治疗组

样本量:

30

Group:

Combination treatment group

Sample size:

干预措施:

针刺联合推拿

干预措施代码:

Intervention:

acupuncture combined with massage

Intervention code:

组别:

对照组

样本量:

30

Group:

control group

Sample size:

干预措施:

针刺

干预措施代码:

Intervention:

acupuncture

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

江西省 

市(区县):

赣州市 

Country:

China

Province:

Jiangxi Province

City:

Ganzhou City

单位(医院):

赣州市中医院 

单位级别:

三甲 

Institution
hospital:

Ganzhou Hospital of Traditional Chinese Medicine

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

颈椎活动度复视检查评分

指标类型:

主要指标

Outcome:

Cervical range of mobility diplopia examination score

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

眼裂宽度

指标类型:

主要指标

Outcome:

Distance between eyelid fissure

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

疗效

指标类型:

主要指标

Outcome:

Curative effect

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

眼球移动距离

指标类型:

次要指标

Outcome:

Eye movement distance

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

瞳孔大小

指标类型:

主要指标

Outcome:

Pupil size

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:

血液

组织:

Sample Name:

Blood

Tissue:

人体标本去向

使用后销毁  

说明

Fate of sample:

Destruction after use  

Note:

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:

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):

SPSS26.0随机数字法

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

SPSS26.0 Random number method

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:

本研究为双盲、随机、对照试验。受试者不知道其分组情况,治疗者不参与数据收集;统计、数据管理人员也不会参与患者的干预。

Blinding:

This study was a double-blinded, randomized, controlled trial. Te subjects had no knowledge of the distribution. Terapists will not be involved in collecting data, and data managers will not articipate in the intervention of patients.

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):

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

Not stated

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:

Not stated

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

Not stated

数据与安全监察委员会:

Data and Safety Monitoring Committee:

暂未确定/Not yet

注册人:

Name of Registration:

 2023-11-24 16:16:30