Treatment of Verruca Plana by external application of tubeimoside injection: a randomized, double-blind, placebo-controlled, multicenter clinical trial.

注册号:

Registration number:

ITMCTR2000003368

最近更新日期:

Date of Last Refreshed on:

2020-06-04

注册时间:

Date of Registration:

2020-06-04

注册号状态:

Registration Status:

预注册

Prospective registration

注册题目:

土贝母皂苷注射液外用治疗扁平疣

Public title:

Treatment of Verruca Plana by external application of tubeimoside injection: a randomized, double-blind, placebo-controlled, multicenter clinical trial.

注册题目简写:

English Acronym:

研究课题的正式科学名称:

土贝母皂苷注射液外用治疗扁平疣的随机、双盲、安慰剂平行对照、多中心临床试验

Scientific title:

A randomized, double-blind, placebo-controlled, multicenter clinical trial of tubeimoside injection for external use in the treatment of Verruca Plana

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:

ChiCTR2000033533 ; ChiMCTR2000003368

申请注册联系人:

安胜

研究负责人:

闫小宁

Applicant:

Sheng An

Study leader:

Xiaoning Yan

申请注册联系人电话:

Applicant telephone:

+86 13384973895

研究负责人电话:

Study leader's telephone:

+86 15529291985

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:

346657832@qq.com

研究负责人电子邮件:

Study leader's E-mail:

xny_sxtcm@126.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:

陕西省西安市高新区光德路8号美德大厦四楼

研究负责人通讯地址:

西安市西华门4号

Applicant address:

Fourth Floor, Meide Building, 8 Guangde Road, High-Tech District, Xi'an, Shaanxi, China

Study leader's address:

4 Xihuamen Road, Xi'an, Shaanxi, China

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:

陕西摩美得气血和制药有限公司

Applicant's institution:

Shaanxi Momentum Qixuehe Pharmaceutcal Company

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:

(2020)伦审第(21)号

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:

陕西省中医医院伦理委员会

Name of the ethic committee:

Ethics Committee of Shaanxi Provincial Hospital of Traditional Chinese Medicine

伦理委员会批准日期:

Date of approved by ethic committee:

2020/6/2 0:00:00

伦理委员会联系人:

史亮

Contact Name of the ethic committee:

Liang Shi

伦理委员会联系地址:

陕西省西安市西华门4号

Contact Address of the ethic committee:

4 Xihuamen Road, Xi'an, Shaanxi, 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:

陕西省中医医院

Primary sponsor:

Shaanxi Provincial Hospital of Traditional Chinese Medicine

研究实施负责(组长)单位地址:

陕西西安市西华门4号

Primary sponsor's address:

4 Xihuamen Road, Xi'an, Shaanxi, 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):

陕西

市(区县):

咸阳

Country:

China

Province:

Shaannxi

City:

Xianyang

单位(医院):

陕西摩美得气血和制药有限公司

具体地址:

高新产业开发区汉仓南路1号

Institution
hospital:

Shaanxi Momentum Qixuehe Pharmaceutcal Company

Address:

1 Hancang Road South, Xianyang High-Tech District

经费或物资来源:

陕西摩美得气血和制药有限公司

Source(s) of funding:

Shaanxi Momentum Qixuehe Pharmaceutical Co., Ltd

研究疾病:

扁平疣

研究疾病代码:

Target disease:

Flat Wart

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:

上市后药物

Post-marketing clinical trial

研究目的:

评价土贝母皂苷注射液外用治疗扁平疣有效性及临床应用的安全性

Objectives of Study:

To evaluate the efficacy and safety of tubeimoside injection in the treatment of Verruca Plana

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 符合扁平疣的西医诊断标准; 2 年龄18-65周岁; 3 皮损发于躯干及四肢; 4 治疗前30日内未用过维A酸类、干扰素类与本病相关的内服药,14天内没用过干扰素类与本病相关的外用药; 5 对本次研究用药不存在禁忌证; 6 签署知情同意者。

Inclusion criteria

1. Patients who meet the diagnostic criteria of Western medicine for verruca plana; 2. Patients aged 18-65 years; 3. Patients with skin lesions on trunk and limbs; 4. Patients who have not used the internal medicine related to this disease, such as vitamin A acid and interferon, have not used the external medicine related to this disease within 30 days before treatment; 5. For the patients without contraindications in this study; 6. Patients signing informed consent.

排除标准:

1 皮疹已经明显融合成片; 2 正处于妊娠及哺乳期的妇女; 3 瘢痕体质以及过敏体质者; 4 合并心、脑、肝、肾、造血系统、内分泌系统等严重原发性疾病患者,其中血ALT、AST>正常值上限1.5倍者,血Cr、BUN> 正常值1.2倍者; 5 合并有神经、精神疾患而无法合作者,以及怀疑或确有酒精、药物滥用史者; 6 HIV感染、肿瘤及免疫力低下的患者; 7 治疗期间有间断者; 8 近1个月参加其他临床试验者。

Exclusion criteria:

1. The patients whose skin rash has obviously fused into pieces; 2. Pregnant and lactating women; 3. Patients with scar constitution and allergic constitution; 4. Patients with serious primary diseases such as heart, brain, liver, kidney, hematopoietic system, endocrine system, etc., in which alt, AST > 1.5 times of the upper limit of normal value, Cr, bun > 1.2 times of the normal value; 5. Patients with neurological and mental disorders who are unable to cooperate, and those who suspect or have a history of alcohol and drug abuse; 6. Patients with HIV infection, tumor and low immunity; 7. Patients with interruption during treatment; 8. Patients who participated in other clinical trials in the past month.

研究实施时间:

Study execute time:

From 2020-06-01

To      2021-06-02

征募观察对象时间:

Recruiting time:

From 2020-06-01

To      2021-06-02

干预措施:

Interventions:

组别:

对照组

样本量:

36

Group:

control group

Sample size:

干预措施:

土贝母皂苷注射液安慰剂

干预措施代码:

Intervention:

Tubeimoside injection placebo

Intervention code:

组别:

试验组

样本量:

36

Group:

experimental group

Sample size:

干预措施:

土贝母皂苷注射液

干预措施代码:

Intervention:

Tubeimoside injection

Intervention code:

样本总量 Total sample size : 72

研究实施地点:

Countries of recruitment
and research settings:

国家:

中国

省(直辖市):

陕西

市(区县):

西安

Country:

China

Province:

Shaanxi

City:

Xi'an

单位(医院):

陕西省中医医院

单位级别:

三级甲等

Institution/hospital:

Shaanxi Traditional Chinese Medicine Hospital

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

陕西

市(区县):

宝鸡

Country:

China

Province:

shaanxi

City:

Baoji

单位(医院):

宝鸡市中心医院

单位级别:

三级甲等

Institution/hospital:

Baoji Central Hospital

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

陕西

市(区县):

西安

Country:

China

Province:

shaanxi

City:

Xi'an

单位(医院):

陕西省人民医院

单位级别:

三级甲等

Institution/hospital:

Shaanxi Provincial People's Hospital

Level of the institution:

Tertiary A

国家:

中国

省(直辖市):

陕西

市(区县):

咸阳

Country:

China

Province:

shaanxi

City:

Xianyang

单位(医院):

陕西中医药大学附属医院

单位级别:

三级甲等

Institution/hospital:

Affiliated Hospital of Shaanxi University of Traditional Chinese medicine

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

疾病疗效

指标类型:

主要指标

Outcome:

Curative Effect of disease

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

皮肤病生活质量量表

指标类型:

次要指标

Outcome:

Quality of life scale for dermatosis

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:

正在进行

Recruiting

年龄范围:

最小 18
Min age years
最大 65
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):

采用以中心为分层因素的分层随机化方法分组,具体操作将由西安交通大学医学院临床药理研究所独立完成和管理.

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

The randomized, central, stratified grouping will be administered by the Institute of Clinical Pharmacology, Xi'an Jiaotong University.

盲法:

双盲

Blinding:

Double blind

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):

Not stated

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:

CRF

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

CRF

数据管理委员会:

Data Managemen Committee:

Yes

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