营养状态对炎症性肠病患者不良临床结局的影响

注册号:

Registration number:

ChiCTR2500104593 

最近更新日期:

Date of Last Refreshed on:

2025-06-19 11:12:59 

注册时间:

Date of Registration:

2025-06-19 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

营养状态对炎症性肠病患者不良临床结局的影响

Public title:

The impact of nutritional status on adverse clinical outcomes in patients with inflammatory bowel disease

注册题目简写:

English Acronym:

研究课题的正式科学名称:

营养状态对炎症性肠病患者不良临床结局的影响

Scientific title:

The impact of nutritional status on adverse clinical outcomes in patients with inflammatory bowel disease

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:

王晓蕾 

研究负责人:

王晓蕾 

Applicant:

Xiaolei Wang 

Study leader:

Xiaolei Wang 

申请注册联系人电话:

Applicant telephone:

+86 138 1726 7967

研究负责人电话:

Study leader's
telephone:

+86 13817267967

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:

xlwang2006@163.com

研究负责人电子邮件:

Study leader's E-mail:

xlwang2006@163.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:

上海市静安区延长中路301号6号楼

研究负责人通讯地址:

上海市静安区延长中路301号6号楼

Applicant address:

Building 6, No. 301, Yanchang Middle Road, Jing'an District, Shanghai

Study leader's address:

Building 6, No. 301, Yanchang Middle Road, Jing'an District, Shanghai

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:

上海市第十人民医院

Applicant's institution:

Shanghai Tenth People's Hospital

研究负责人所在单位:

上海市第十人民医院

Affiliation of the Leader:

Shanghai Tenth People's Hospital

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:

SHSY-IEC-6.0/25K68/P01

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:

上海市第十人民医院伦理委员会

Name of the ethic committee:

Ethics Committee of Shanghai tenth People's Hospital

伦理委员会批准日期:

Date of approved by ethic committee:

2025-04-21 00:00:00

伦理委员会联系人:

袁凤

Contact Name of the ethic committee:

Feng Yuan

伦理委员会联系地址:

上海市静安区延长中路301号6号楼

Contact Address of the ethic committee:

Building 6, No. 301, Yanchang Middle Road, Jing'an District, Shanghai

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 21 6630 1604

伦理委员会联系人邮箱:

Contact email of the ethic committee:

shsyiec@126.com

研究实施负责(组长)单位:

上海市第十人民医院

Primary sponsor:

Shanghai Tenth People's Hospital

研究实施负责(组长)单位地址:

上海市静安区延长中路301号6号楼

Primary sponsor's address:

Building 6, No. 301, Yanchang Middle Road, Jing'an District, Shanghai

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):

上海市第十人民医院

具体地址:

上海市静安区延长中路301号6号楼

Institution
hospital:

Shanghai Tenth People's Hospital

Address:

Building 6, No. 301, Yanchang Middle Road, Jing'an District, Shanghai

经费或物资来源:

自选课题(自筹)

Source(s) of funding:

Self-selected project (self-funded)

研究疾病:

炎症性肠病  

Target disease:

inflammatory bowel disease

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:

其它 

Study phase:

N/A

研究设计:

连续入组 

Study design:

Sequential 

研究目的:

观察不同营养状态对炎症性肠病患者不良临床结局的影响。  

Objectives of Study:

To observe the effect of different nutritional status on adverse clinical outcomes in patients with inflammatory bowel disease.

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:

1.①患者拒绝接受营养检测; ②备孕、妊娠及哺乳患者; ③存在短肠综合征或严重消耗性疾病,例如肿瘤、甲状腺功能亢进等; ④存在心脏、肾脏相关慢性疾病病史; ⑤患者正在接受肠外营养治疗; ⑥失访或缺乏完整临床资料。

Exclusion criteria:

1.Patients who refuse to undergo nutritional testing; 2. Preparation for pregnancy, pregnancy and breastfeeding patients; 3.Presence of short bowel syndrome or severe wasting disease, e.g., tumour, hyperthyroidism; 4. Existence of cardiac and renal-related chronic disease history; 5.The patient is receiving parenteral nutrition therapy; 6.Missed visits or lack of complete clinical information.

研究实施时间:

Study execute time:

From 2024-11-01 00:00:00 To 2026-04-01 00:00:00  

征募观察对象时间:

Recruiting time:

From 2025-06-20 00:00:00 To 2025-12-31 00:00:00

干预措施:

Interventions:

组别:

炎症性肠病患者

样本量:

300

Group:

Patients with inflammatory bowel disease

Sample size:

干预措施:

干预措施代码:

Intervention:

None

Intervention code:

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):

上海市第十人民医院 

单位级别:

三级甲等 

Institution
hospital:

Shanghai Tenth People's Hospital

Level of the institution:

Tertiary A

测量指标:

Outcomes:

指标中文名:

药物诱导缓解活动期CD患者3个月的临床应答率

指标类型:

次要指标

Outcome:

Clinical response rate at 3 months in patients with active CD in drug-induced remission

Type:

Secondary indicator

测量时间点:

3个月

测量方法:

CD患者CDAI评分,UC患者改良Mayo评分

Measure time point of outcome:

three months

Measure method:

CDAI for CD patients and modified Mayo scores for UC patients

指标中文名:

自营养诊断后随访6个月至1年期间不良临床结局的发生率

指标类型:

主要指标

Outcome:

Incidence of adverse clinical outcomes between 6 months and 1 year follow-up from nutritional diagnosis

Type:

Primary indicator

测量时间点:

6个月及1年

测量方法:

电话随访

Measure time point of outcome:

six months and a year

Measure method:

telephone follow-up visit

指标中文名:

人体成分分析核心指标

指标类型:

次要指标

Outcome:

Core indicators for body composition analysis

Type:

Secondary indicator

测量时间点:

基线

测量方法:

生物电阻抗方法

Measure time point of outcome:

baseline

Measure method:

BIA

指标中文名:

评估患者生活质量改善的情况

指标类型:

次要指标

Outcome:

Assessment of improvement in patients' quality of life

Type:

Secondary indicator

测量时间点:

6个月及1年

测量方法:

炎症性肠病问卷量表

Measure time point of outcome:

six months and a year

Measure method:

Inflammatory Bowel Disease Questionnaire(IBD-Q)

指标中文名:

药物诱导缓解活动期肛瘘改善情况

指标类型:

次要指标

Outcome:

Drug-induced improvement in remission of active anal fistulae

Type:

Secondary indicator

测量时间点:

3个月

测量方法:

肛周疾病活动评分

Measure time point of outcome:

three months

Measure method:

perianal disease activity index(PDAI)

指标中文名:

药物诱导缓解3个月后活动期CD患者的内镜缓解率

指标类型:

次要指标

Outcome:

Endoscopic remission rates in patients with active CD 3 months after drug-induced remission

Type:

Secondary indicator

测量时间点:

3个月

测量方法:

内镜检查

Measure time point of outcome:

three months

Measure method:

endoscopy

采集人体标本:

Collecting sample(s)
from participants:

标本中文名:

尿液

组织:

Sample Name:

urine

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 14 years
最大 Max age 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:

不公开/Private

盲法:

Blinding:

None

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):

2031年4月,临床试验公共管理平台 http://www.medresman.org.cn/login.aspx

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

Date:April 2031,ResMan http://www.medresman.org.cn/login.aspx

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:

病历记录表

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

Case record form

数据与安全监察委员会:

Data and Safety Monitoring Committee:

有/Yes

注册人:

Name of Registration:

 2025-06-19 11:12:26