10.6-μm Infrared Laser as Adjuvant Therapy for Diabetic Peripheral Neuropathy: a Double-Blind, Randomized Controlled Trial

注册号:

Registration number:

ITMCTR2000002935

最近更新日期:

Date of Last Refreshed on:

2020-01-25

注册时间:

Date of Registration:

2020-01-25

注册号状态:

Registration Status:

预注册

Prospective registration

注册题目:

10.6μm激光灸治疗糖尿病周围神经病变随机对照临床试验

Public title:

10.6-μm Infrared Laser as Adjuvant Therapy for Diabetic Peripheral Neuropathy: a Double-Blind, Randomized Controlled Trial

注册题目简写:

English Acronym:

研究课题的正式科学名称:

10.6μm激光灸治疗糖尿病周围神经病变随机对照临床试验

Scientific title:

10.6-μm Infrared Laser as Adjuvant Therapy for Diabetic Peripheral Neuropathy: a Double-Blind, Randomized Controlled Trial

研究课题的正式科学名称简写:

Scientific title acronym:

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:

ChiCTR2000029329 ; ChiMCTR2000002935

申请注册联系人:

林琳

研究负责人:

沈雪勇

Applicant:

Lin Lin

Study leader:

Xueyong Shen

申请注册联系人电话:

Applicant telephone:

+86 18616781529

研究负责人电话:

Study leader's telephone:

+86 02151322173

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:

527116245@qq.com

研究负责人电子邮件:

Study leader's E-mail:

snowysh@hotmail.com

申请单位网址(自愿提供):

Study leader's 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:

上海浦东新区蔡伦路1200号

研究负责人通讯地址:

上海浦东新区蔡伦路1200号

Applicant address:

1200 Cailun Road, Pudong New District, Shanghai, China

Study leader's address:

1200 Cailun Road, Pudong New District, Shanghai, China

申请注册联系人邮政编码:

Applicant postcode:

201203

研究负责人邮政编码:

Study leader's postcode:

申请人所在单位:

上海中医药大学

Applicant's institution:

Shanghai University of Traditional Chinese Medicine

是否获伦理委员会批准:

Approved by ethic committee:

伦理委员会批件文号:

Approved No. of ethic committee:

2019SHL-KY-37

伦理委员会批件附件:

Approved file of Ethical Committee:

View

批准本研究的伦理委员会名称:

上海市中医医院伦理委员会

Name of the ethic committee:

IRB of Shanghai Municipal Hospital of Traditional Chinese Medicine

伦理委员会批准日期:

Date of approved by ethic committee:

2019/12/25 0:00:00

伦理委员会联系人:

凌丽

Contact Name of the ethic committee:

Li Ling

伦理委员会联系地址:

上海市芷江中路274号

Contact Address of the ethic committee:

274 Middle Zhijiang Road, Shanghai, China

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:

上海市中医医院

Primary sponsor:

Shanghai Municipal Hospital of Traditional Chinese Medicine

研究实施负责(组长)单位地址:

上海市芷江中路274号

Primary sponsor's address:

274 Middle Zhijiang Road, Shanghai, China

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

上海市

市(区县):

Country:

China

Province:

Shanghai

City:

单位(医院):

上海中医药大学

具体地址:

蔡伦路1200号

Institution
hospital:

Shanghai University of Traditional Chinese Medicine

Address:

1200 Cailun Road

经费或物资来源:

上海中医药大学师资博士后资助项目

Source(s) of funding:

Postdoctoral program for persons qualified to teach of Shanghai University of traditional Chinese Medicine

研究疾病:

糖尿病周围神经病变

研究疾病代码:

Target disease:

Diabetic peripheral Neuropathy

Target disease code:

研究类型:

Study type:

干预性研究

Interventional study

研究设计:

Study design:

随机平行对照

randomized controlled trial(parallel group design)

研究所处阶段:

Study phase:

探索性研究/预试验

Pilot clinical trial

研究目的:

本课题拟开展随机双盲对照试验,来验证10.6μm激光灸对糖尿病周围神经病变的有效性和安全性,为临床实践提供科学的证据。

Objectives of Study:

The purpose of this placebo controlled clinical trial is to determine the effect and safety of 10.6-μm laser moxibustion in patients with DPN.

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) 符合糖尿病周围神经病变诊断标准的患者,且周围神经病变症状主要以以下肢为主; 2) 年龄在18-75岁之间,男女不限; 3) 肌电图示双下肢神经传导速度延迟; 4) 血糖水平控制在稳定范围内,空腹血糖≤7.0 mmol/L,餐后2h血糖≤8 mmol/L,糖化血红蛋白≤7%; 5) 理解试验过程,并自愿签署知情同意书者;

Inclusion criteria

(1) diagnosed with DPN in both lower extremities; (2) aged 18–75 years old, no limit on gender; (3) delayed nerve conduction velocity in lower extremities; (4) stable levels of blood glucose level (FPG <= 7.0 mmol/L2hPBG <= 8 mmol/LHbA1c <= 7%); (5) understanding and signing the informed consent.

排除标准:

1) 由糖尿病以外的疾病引起的神经病变(如酗酒、化疗、遗传原因、慢性炎症或特发性神经病变等); 2) 妨碍参与和影响研究完成的疾病,如过去3个月内患有心梗或中风、充血性心力衰竭、严重COPD、癌症、严重的全身性疾病及严重精神疾病等; 3) 周围神经病变主要发生在上肢; 4) 皮肤溃疡、或其他皮肤病不宜使用激光灸治疗者; 5) 近3个月下肢骨折患者,或曾做过髋关节或膝关节置换术者; 6) 过去3个月内接受过针灸治疗; 7) 过去3个月内接受过低强度激光治疗; 8) 同时使用其他外用治疗者; 9) 不愿意被随机分组; 10) 由于各种原因而无法理解或完成量表者; 11) 同时参与其他临床试验的患者; 12) 妊娠、哺乳期妇女; 13) 滥用止痛药或有酗酒情况的患者。

Exclusion criteria:

(1) neuropathy or chronic pain caused by conditions other than diabetes; (2) DPN most prevalent in the upper limbs; (3) Presence of serious medical conditions, including kidney diseases, heart diseases, pulmonary diseases, liver diseases or contagious diseases, or malignant tumors and serious psychopathy; (4) Previous history of knee/hip replacement surgery or bone fracture of the lower extremities during the last 3 months and other conditions that would confound assessment of neuropathy; (5) Ulceration and other diseases at the lower extremities; (6) Acupuncture or moxibustion treatment received in the previous 3 months; (7) LLLT received in the previous 3 months; (8) Using other external therapy simultaneously; (9) Opiate, analgesic, illicit drug or alcohol abuse; (10) Unwillingness to be randomly assigned into either a treatment or a placebo group; (11) Unable to fill measurement questionnaires; (12) Recruited in other clinical trial simultaneously; (13) Pregnant or breast-feeding women.

研究实施时间:

Study execute time:

From 2020-02-17

To      2022-02-17

征募观察对象时间:

Recruiting time:

From 2020-02-17

To      2022-02-17

干预措施:

Interventions:

组别:

假激光灸组

样本量:

57

Group:

sham LM group

Sample size:

干预措施:

假激光灸治疗结合中西医药物

干预措施代码:

Intervention:

sham laser moxibustion therapy combined with Chinese and Western Medicine

Intervention code:

组别:

10.6μm激光灸组

样本量:

57

Group:

the LM group

Sample size:

干预措施:

激光灸治疗结合中西医药物

干预措施代码:

Intervention:

10.6μm laser moxibustion therapy combined with Chinese and Western Medicine

Intervention code:

样本总量 Total sample size : 114

研究实施地点:

Countries of recruitment
and research settings:

国家:

中国

省(直辖市):

上海市

市(区县):

Country:

China

Province:

Shanghai

City:

单位(医院):

上海市中医医院

单位级别:

三级甲等

Institution/hospital:

Shanghai Municipal Hospital of Traditional Chinese Medicine

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

神经传导速度

指标类型:

主要指标

Outcome:

Nerve Conduction Velocity

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

密西根神经病变筛选量表

指标类型:

次要指标

Outcome:

Michigan Neuropathy Screening Instrument

Type:

Secondary 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:

尚未开始

Not yet recruiting

年龄范围:

最小
Min age years
最大
Max age years

Recruiting status:

Participant age:

性别:

Gender:

男女均可

Both

随机方法(请说明由何人用什么方法产生随机序列):

由不参与试验其他过程的研究人员利用SPSS软件产生随机分配序列。

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

The random assignment sequence is generated by the researcher who does not participate in other processes of the trial using SPSS software.

盲法:

单盲

Blinding:

Blind method for subjects.

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):

2022.8.17公开,原始数据

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

Aug,17,2022, metadata

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:病例记录表 数据管理:SPSS软件

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

Data collection:record Data management:SPSS

数据管理委员会:

Data Managemen Committee:

暂未确定

Not yet

研究计划书或研究结果报告发表信息
(杂志名称、期、卷、页,时间;或网址):

Publication information of the protocol/research results report
(name of the journal, volume, issue, pages, time; or website):

ITMCTR BJ-ICP:07032215-5 Tip: IE8 is recommended Use the system with widescreen display resolution above