生物制剂联合肛瘘内口闭合夹治疗克罗恩病肛瘘的临床研究

注册号:

Registration number:

ChiCTR2400087786 

最近更新日期:

Date of Last Refreshed on:

2024-08-05 10:54:31 

注册时间:

Date of Registration:

2024-08-05 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

生物制剂联合肛瘘内口闭合夹治疗克罗恩病肛瘘的临床研究

Public title:

Clinical study on the treatment of Crohn's disease anal fistula with biologics combined with anal fistula closure clip

注册题目简写:

English Acronym:

研究课题的正式科学名称:

生物制剂联合肛瘘内口闭合夹治疗克罗恩病肛瘘的临床研究

Scientific title:

Clinical study on the treatment of Crohn's disease anal fistula with biologics combined with anal fistula closure clip

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:

王浩 

研究负责人:

王浩 

Applicant:

Hao Wang 

Study leader:

Hao Wang 

申请注册联系人电话:

Applicant telephone:

+86 159 5489 9305

研究负责人电话:

Study leader's
telephone:

+86 138 5165 6633

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:

cnzhwh@126.com

研究负责人电子邮件:

Study leader's E-mail:

cnzhwh@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:

江苏省南京市秦淮区汉中路155号

研究负责人通讯地址:

江苏省南京市秦淮区汉中路155号

Applicant address:

155 Hanzhong Road, Qinhuai District, Nanjing, Jiangsu

Study leader's address:

155 Hanzhong Road, Qinhuai District, Nanjing, Jiangsu

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:

南京中医药大学附属医院(江苏省中医院)

Applicant's institution:

Nanjing University of Traditional Chinese Medicine Affiliated Hospital (Jiangsu Provincial Hospital of Traditional Chinese Medicine)

研究负责人所在单位:

南京中医药大学附属医院(江苏省中医院)

Affiliation of the Leader:

Nanjing University of Traditional Chinese Medicine Affiliated Hospital (Jiangsu Provincial 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:

2024NL-128-02

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:

南京中医药大学附属医院(江苏省中医院)伦理委员会

Name of the ethic committee:

Ethics Committee of Nanjing University of Traditional Chinese Medicine Affiliated Hospital (Jiangsu Provincial Hospital of Traditional Chinese Medicine)

伦理委员会批准日期:

Date of approved by ethic committee:

2024-07-16 00:00:00

伦理委员会联系人:

王卯

Contact Name of the ethic committee:

Mao Wang

伦理委员会联系地址:

江苏省南京市秦淮区汉中路155号

Contact Address of the ethic committee:

155 Hanzhong Road, Qinhuai District, Nanjing, Jiangsu

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 28 0656 0515

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:

南京中医药大学附属医院(江苏省中医院)

Primary sponsor:

Nanjing University of Traditional Chinese Medicine Affiliated Hospital (Jiangsu Provincial Hospital of Traditional Chinese Medicine)

研究实施负责(组长)单位地址:

江苏省南京市秦淮区汉中路155号

Primary sponsor's address:

155 Hanzhong Road, Qinhuai District, Nanjing, Jiangsu

试验主办单位(项目批准或申办者):

Secondary sponsor:

国家:

中国

省(直辖市):

江苏省

市(区县):

南京市

Country:

CHINA

Province:

Jiangsu

City:

NanJing

单位(医院):

南京中医药大学附属医院(江苏省中医院)

具体地址:

秦淮区汉中路155号

Institution
hospital:

Nanjing University of Traditional Chinese Medicine Affiliated Hospital (Jiangsu Provincial Hospital of Traditional Chinese Medicine)

Address:

155 Hanzhong Road, Qinhuai District, Nanjing, Jiangsu

经费或物资来源:

自筹

Source(s) of funding:

Self-funded

研究疾病:

瘘管型肛周克罗恩病  

Target disease:

perianal fistulizing Crohn's disease

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:

单臂 

Study design:

Single arm 

研究目的:

评价生物制剂联合肛瘘内口闭合夹治疗克罗恩病肛瘘的临床疗效  

Objectives of Study:

Evaluate the clinical efficacy of biologics combined with anal fistula closure clip in the treatment of Crohn's disease anal fistula

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.妊娠期、哺乳期女性; 2.直肠、肛管有严重感染者; 3.有严重的心、肝、肾疾患及凝血功能障碍(包括正在进行抗凝治疗)、有盆腔放疗史、严重免疫功能缺陷、近期(3个月内)肛瘘部位行硬化剂注射治疗史者; 4.精神异常、认知和沟通障碍者,或精神高度紧张不合作者; 5.病例资料不全者; 6.医护人员判断其他不适合使用者;

Exclusion criteria:

1. Pregnant or lactating women; 2. Individuals with severe infections in the rectum and anal canal; 3. Individuals with severe heart, liver, kidney diseases and coagulation dysfunction (including those undergoing anticoagulant therapy), a history of pelvic radiation therapy, severe immune dysfunction, and a recent (within 3 months) history of sclerosing agent injection therapy at the anal fistula site; 4. Individuals with mental abnormalities, cognitive and communication disorders, or high levels of mental stress that do not conform to the author's requirements; 5. Individuals with incomplete case information; 6. Medical staff determine that other users are not suitable;

研究实施时间:

Study execute time:

From 2024-07-16 00:00:00 To 2025-07-16 00:00:00  

征募观察对象时间:

Recruiting time:

From 2024-08-15 00:00:00 To 2025-07-01 00:00:00

干预措施:

Interventions:

组别:

试验组组

样本量:

30

Group:

Experimental group

Sample size:

干预措施:

生物制剂联合肛瘘内口闭合夹

干预措施代码:

Intervention:

Biologics combined with anal fistula closure clip

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

江苏省 

市(区县):

南京市 

Country:

China

Province:

Jiangsu

City:

Nanjing

单位(医院):

南京中医药大学附属医院(江苏省中医院) 

单位级别:

三甲 

Institution
hospital:

Nanjing University of Traditional Chinese Medicine Affiliated Hospital (Jiangsu Provincial Hospital of Traditional Chinese Medicine)

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

瘘管临床愈合率

指标类型:

主要指标

Outcome:

Clinical healing rate of fistula

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

瘘管应答率

指标类型:

次要指标

Outcome:

Fistula response rate

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

瘘管影像学愈合率

指标类型:

主要指标

Outcome:

Healing rate of fistula imaging

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

CD临床缓解率

指标类型:

主要指标

Outcome:

Clinical remission rate of CD

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

内镜缓解率

指标类型:

主要指标

Outcome:

Endoscopic remission rate

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

CD临床应答率

指标类型:

次要指标

Outcome:

CD clinical response rate

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

内镜应答率

指标类型:

次要指标

Outcome:

Endoscopic response rate

Type:

Secondary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

肛门括约功能的状态

指标类型:

次要指标

Outcome:

The state of anal sphincter function

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:

肛周瘘管

组织:

Sample Name:

Perianal fistula

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:

尚未开始

Not yet recruiting

年龄范围:

Participant age:

最小 Min age 18 years
最大 Max age 65 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):

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

None

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:

None

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

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):

2026年10月 向主研人申请

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

Apply to the principal investigator in October 2026

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:

病例记录表,电子采集和管理系统

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

Case record form, electronic collection and management system

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:

 2024-08-05 10:54:17