|
注册号: Registration number: |
ChiCTR2000031686 |
|
最近更新日期: Date of Last Refreshed on: |
2020-04-09 11:27:15 |
|
注册时间: Date of Registration: |
2020-04-07 00:00:00 |
|
注册号状态: |
预注册 |
|
Registration Status: |
Prospective registration |
|
注册题目: |
浮刺埋线治疗带状疱疹后遗神经痛的临床疗效及机制研究 |
|
Public title: |
Clinical Effect and Mechanism of Absorbable Suture Floating Implantation on Postherpetic Neuralgia |
|
注册题目简写: |
|
|
English Acronym: |
|
|
研究课题的正式科学名称: |
浮刺埋线治疗带状疱疹后遗神经痛的临床疗效及机制研究 |
|
Scientific title: |
Clinical Effect and Mechanism of Absorbable Suture Floating Implantation on Postherpetic 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: |
ChiMCTR2000003192 |
|
申请注册联系人: |
李庄 |
研究负责人: |
李庄 |
|
Applicant: |
Li Zhuang |
Study leader: |
Li Zhuang |
|
申请注册联系人电话: Applicant telephone: |
+86 15820406568 |
研究负责人电话:
Study leader's |
+86 15820406568 |
|
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: |
lilylee206@email.szu.edu.cn |
研究负责人电子邮件: Study leader's E-mail: |
lilylee206@email.szu.edu.cn |
|
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: |
深圳市福田区振华路2号深圳大学第一附属医院中西医结合分院治未病中心 |
研究负责人通讯地址: |
深圳市福田区振华路2号深圳大学第一附属医院中西医结合分院治未病中心 |
|
Applicant address: |
The First Affiliated Hospital of Shenzhen University, 2 Zhenhua Road, Futian District, Shenzhen, Guangdong |
Study leader's address: |
The First Affiliated Hospital of Shenzhen University, 2 Zhenhua Road, Futian District, Shenzhen, Guangdong |
|
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: |
广州中医药大学 |
||
|
Applicant's institution: |
Guangzhou University of Chinese Medicine |
||
|
研究负责人所在单位: |
广州中医药大学 |
||
|
Affiliation of the Leader: |
Guangzhou University of Chinese Medicine |
||
|
是否获伦理委员会批准: |
是 |
||
|
Approved by ethic committee: |
Yes |
||
|
伦理委员会批件文号: Approved No. of ethic committee: |
Y[2019]261 |
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: |
广州中医药大学第一附属医院伦理委员会 |
||
|
Name of the ethic committee: |
Ethics Committee of the First Affiliated Hospital of Guangzhou University of Chinese Medicine |
||
|
伦理委员会批准日期: Date of approved by ethic committee: |
2019-10-21 00:00:00 | ||
|
伦理委员会联系人: |
黎老师 |
||
|
Contact Name of the ethic committee: |
Teacher Li |
||
|
伦理委员会联系地址: |
广东省广州市白云区机场路6号广州中医药大学第一附属医院伦理委员会 |
||
|
Contact Address of the ethic committee: |
Ethics Committee of the First Affiliated Hospital of Guangzhou University of Chinese Medicine, 6 Jichang Road, Baiyun District, Guangzhou, Guangdong |
||
|
伦理委员会联系人电话: Contact phone of the ethic committee: |
+86 020-36588667, +86 020-36591965 |
伦理委员会联系人邮箱: Contact email of the ethic committee: |
gztcmlunli@163.com |
|
研究实施负责(组长)单位: |
广州中医药大学第一附属医院 |
||||||||||||||||||||||||||||||||||||||||||||
|
Primary sponsor: |
The First Affiliated Hospital of Guangzhou University of Chinese Medicine |
||||||||||||||||||||||||||||||||||||||||||||
|
研究实施负责(组长)单位地址: |
广东省广州市白云区机场路6号 |
||||||||||||||||||||||||||||||||||||||||||||
|
Primary sponsor's address: |
6 Jichang Road, Baiyun District, Guangzhou, Guangdong |
||||||||||||||||||||||||||||||||||||||||||||
|
试验主办单位(项目批准或申办者): Secondary sponsor: |
|
||||||||||||||||||||||||||||||||||||||||||||
|
经费或物资来源: |
国自然面上项目 ( 81574061), 深圳三名工程 ( SZSM201612049)。 |
||||||||||||||||||||||||||||||||||||||||||||
|
Source(s) of funding: |
National Nature Sceience Foudation of China (81574061); Three Leading Projects Fund of Shenzhen (SZSM201612049). |
||||||||||||||||||||||||||||||||||||||||||||
|
研究疾病: |
带状疱疹后遗神经痛 |
||||||||||||||||||||||||||||||||||||||||||||
|
Target disease: |
Postherpetic Neuralgia |
||||||||||||||||||||||||||||||||||||||||||||
|
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: |
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: |
1.治疗2疗程(8周后)对患者视觉模拟量表(VAS)、匹兹堡睡眠质量指数评分、抑郁自评量表(SDS),评估浮刺埋线的临床疗效,为临床治疗PHN提供治疗思路; 2. 通过PHN患者治疗2疗程(8周)前后Th1、Th2、Th17、Treg细胞的的变化,验证其是否参与PHN的发病,并探讨Th1、Th2、Th17、Treg细胞在PHN发病过程中的作用,完善PHN发病的免疫机制,为指导临床工作提供实验室依据,提供新的免疫思路; |
||||||||||||||||||||||||||||||||||||||||||||
|
Objectives of Study: |
1. Two courses of treatment (after eight weeks). The patient's visual analog scale (VAS), Pittsburgh Sleep Quality Index score, and depression self-rating scale (SDS) were used to evaluate the clinical efficacy of the embossed line. Ideas; 2. Through the changes of Th1, Th2, Th17, and Treg cells before and after two courses of treatment (eight weeks) in PHN patients, verify whether they are involved in the pathogenesis of PHN, and explore the Th1, Th2, Th17, and Treg cells in the pathogenesis of PHN Role, improve the immune mechanism of PHN pathogenesis, provide laboratory basis for guiding clinical work, and provide new ideas for immunization. |
||||||||||||||||||||||||||||||||||||||||||||
|
药物成份或治疗方案详述: |
1. 治疗组(浮刺埋线)1)取穴:局部阿是穴及夹脊穴:T1至L5棘突旁开0.5寸,本研究选取神经痛发生所属相应神经节段的夹脊穴。按照国家技术监督局发布的《中华人民共和国国家标准·经穴部位》(GB 12346-2006)中的穴位定位取穴。 2)操作方法: ① 浮刺埋线:取穴:局部阿是穴;方法:局部皮肤行常规消毒,以一次性7号无菌注射针头作埋线套管,取华佗牌3-0(可吸收性外科缝线),于注射针头前端放置并折叠。左手绷紧或捏起局部皮肤,右手将针头与肌肤约呈15°进针,针体在浅筋膜层滑行,进针时针尖所经之处皮肤微微隆起,沿神经走向刺入约20mm,以进针点为支点, 手握针柄, 左右摇摆, 使针体作扇形运动, 持续10-20s, 运针完毕,退针的同时将线体埋植在皮下穴位的浅筋膜层。 ② 夹脊深刺埋线:选穴:神经痛发生所属相应神经节段的夹脊穴;方法:消毒、针具及持针方法同浮刺埋线,右手将针头略向椎体倾斜约15°,刺入到所需深度。将线体埋植在穴位的皮下约0.8-1.5寸的深度。每2周治疗一次,2次为一疗程,共治疗2疗程。 2. 对照组(西药组) 药物:普瑞巴林(辉瑞制药有限公司,75mg/片,国药准字级0100102)。 方法:口服每次75mg,每日两次,2周一疗程,共2疗程。 |
||||||||||||||||||||||||||||||||||||||||||||
|
Description for medicine or protocol of treatment in detail: |
|
||||||||||||||||||||||||||||||||||||||||||||
|
纳入标准: |
|||||||||||||||||||||||||||||||||||||||||||||
|
Inclusion criteria |
|||||||||||||||||||||||||||||||||||||||||||||
|
排除标准: |
1.特殊类型带状疱疹(HZ)继发的后遗神经痛,包括眼耳、内脏、脑膜、泛发性、无疹型HZ等所致后遗神经痛; |
||||||||||||||||||||||||||||||||||||||||||||
|
Exclusion criteria: |
1. Sequela neuralgia secondary to special types of herpes zoster (HZ), including sciatica caused by eyes, ears, internal organs, meninges, generalized, non-rash type HZ; |
||||||||||||||||||||||||||||||||||||||||||||
|
研究实施时间: Study execute time: |
从 From 2020-04-13 00:00:00至 To 2020-09-30 00:00:00 |
征募观察对象时间: Recruiting time: |
从 From 2020-05-06 00:00:00 至 To 2020-08-31 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): |
随机:将入选患者采用随机数字表法分为治疗组(浮刺埋线)、对照组(普瑞巴林)。 随机数字表法: ①编号:严格按照诊断标准、纳入标准和排除标准筛选病例,确定纳入后,按照患者入组时间的先后顺序,编号1-64; ②获取随机数字:从随机数字表中任意一个数字开始,沿同一方向顺序获取每位受试者一个随机数字; ③求余数:随机数字除以组数n(n=2)求余数,若可整除则余数取组数n=2; ④分组:按余数分组,余数为1者为治疗组,余数为2者为对照组; ⑤调整:若分组后例数不均,假如有m例需要调整,需要从中抽取1例,在随机表中续抄1个数字,除以m后将得到的余数作为所抽取受试者的组别。(若整除余数取m)。 ⑥将编号1-64的64个信封,分别装入1-N号受试者的分组情况,并密封,待受试者进入临床试验时当场开启。 |
||||||||
|
Randomization Procedure (please state who generates the random number sequence and by what method): |
The random sequece were generated by using random number table. |
||||||||
|
是否公开试验完成后的统计结果: Calculated Results after the Study Completed public access: |
不公开/Private |
|
盲法: |
检测者、统计者对患者的分组设盲。 |
|
Blinding: |
Blind methof for evaluators and statisticians. |
|
是否共享原始数据: IPD sharing |
是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): |
CNKI博士论文中公开 |
|
The way of sharing IPD”(include metadata and protocol, If use web-based public database, please provide the url): |
The datas will be published in the CNKI doctoral thesis |
|
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: |
数据的采集采用CRF病历记录表,由两位研究者一起进行登记。 |
|
Data collection and Management (A standard data collection and management system include a CRF and an electronic data capture: |
The data was collected using a CRF medical record form, which was registered by two researchers. |
|
数据与安全监察委员会: Data and Safety Monitoring Committee: |
有/Yes |