请结合研究计划书完善测量指标的填写。该研究尚未获得伦理委员会批准,请于批准后再开始纳入参试者,并与我们联系上传批件。 超声引导下颈交感神经阻滞对眼部神经痛的治疗观察

注册号:

Registration number:

ChiCTR2200058709 

最近更新日期:

Date of Last Refreshed on:

2023-03-12 20:49:20 

注册时间:

Date of Registration:

2022-04-14 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

请结合研究计划书完善测量指标的填写。该研究尚未获得伦理委员会批准,请于批准后再开始纳入参试者,并与我们联系上传批件。 超声引导下颈交感神经阻滞对眼部神经痛的治疗观察

Public title:

Observation of ultrasound-guided cervical sympathetic block in the treatment of ocular neuralgia

注册题目简写:

English Acronym:

研究课题的正式科学名称:

超声引导下颈交感神经阻滞对眼部神经痛的治疗观察

Scientific title:

Observation of ultrasound-guided cervical sympathetic block in the treatment of ocular neuralgia

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:

李秀华 

研究负责人:

王古岩 

Applicant:

xiuhua li 

Study leader:

Guyan Wang 

申请注册联系人电话:

Applicant telephone:

15910771590

研究负责人电话:

Study leader's
telephone:

13910985139

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:

life9708lxh@126.com

研究负责人电子邮件:

Study leader's E-mail:

life9708lxh@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:

北京市东城区东交民巷1号

研究负责人通讯地址:

北京市东城区东交民巷1号

Applicant address:

No1 Dongjiaomin Lane, Dongcheng District, Beijing

Study leader's address:

No1 Dongjiaomin Lane, Dongcheng District, Beijing

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:

北京同仁医院

Applicant's institution:

Tongren Hospital, Beijing

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:

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:

北京同仁医院

Primary sponsor:

Tongren Hospital, Beijing

研究实施负责(组长)单位地址:

北京市东城区东交民巷1号

Primary sponsor's address:

o1 Dongjiaomin Lane, Dongcheng District, Beijing

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

北京

市(区县):

Country:

China

Province:

Beijing

City:

单位(医院):

北京同仁医院

具体地址:

北京市东城区东交民巷1号

Institution
hospital:

Tongren Hospital

Address:

o1 Dongjiaomin Lane, Dongcheng District, Beijing

经费或物资来源:

Source(s) of funding:

No

研究疾病:

神经病理性疼痛  

Target disease:

neuropathic pain

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:

治疗新技术临床试验 

Study phase:

New Treatment Measure Clinical Study

研究设计:

病例对照研究 

Study design:

Case-Control study 

研究目的:

观察颈上交感神经节阻滞镇痛术对眼及眼周痛的作用及疗效,多学科多模式治疗复杂性难治性眼痛,缓解患者的紧张焦虑,提高患者的生活质量  

Objectives of Study:

To observe the effect and efficacy of superior cervical sympathetic ganglion block on eye pain and periocular pain, to treat complicated and refractory eye pain with multi-discipline, to relieve patients' tension and anxiety, and improve their quality of life.

药物成份或治疗方案详述:

 

Description for medicine or protocol of treatment in detail:

 

纳入标准:

Inclusion criteria

排除标准:

(1)出凝血障碍、穿刺部位感染;
(2)心脏束支传导阻滞的患者;
(3)孕妇及不能配合操作的患者;
(4)不同意参与观察,患者或家属拒绝签署知情同意书。

Exclusion criteria:

(1) Coagulation disorder and infection of puncture site;
(2) patients with heart bundle branch block;
(3) pregnant women and patients who cannot cooperate with the operation;
(4) Patients or their family members refuse to sign informed consent when they do not agree to participate in observation.

研究实施时间:

Study execute time:

From 2022-07-01 00:00:00 To 2023-07-01 00:00:00  

征募观察对象时间:

Recruiting time:

From 2022-07-31 00:00:00 To 2024-01-31 00:00:00

干预措施:

Interventions:

组别:

1

样本量:

36

Group:

one

Sample size:

干预措施:

星状神经节阻滞

干预措施代码:

Intervention:

stellate ganglion block

Intervention code:

组别:

2

样本量:

36

Group:

two

Sample size:

干预措施:

颈上交感神经节阻滞

干预措施代码:

Intervention:

Supracervical sympathetic ganglion block

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

北京 

市(区县):

 

Country:

China

Province:

Beijing

City:

单位(医院):

北京同仁医院 

单位级别:

三级甲等 

Institution
hospital:

Tongren Hospital

Level of the institution:

Grade A, Class 3 Hospital

测量指标:

Outcomes:

指标中文名:

疼痛评分<3的时间

指标类型:

主要指标

Outcome:

time of pain score<3

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:

No

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 18 years
最大 Max age 90 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):

统计分析人员根据计算机自动分析产生分组,统计软件Ralloc版本3.5.2 (Statacorp College Station, TX, USA)

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

Statistical analyst used a computer generated allocation sequence from Statistical Software Stata 10.0 module Ralloc version 3.5.2 (Statacorp College Station, TX, USA)

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):

2024.07

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

2024.07

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:

CRF

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

CRF

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2022-04-14 23:48:37