能量补充剂对维持性血液透析患者营养状态的影响

注册号:

Registration number:

ChiCTR1800015068 

最近更新日期:

Date of Last Refreshed on:

2018-03-06 12:26:58 

注册时间:

Date of Registration:

2018-03-06 00:00:00 

注册号状态:

预注册

Registration Status:

Prospective registration

注册题目:

能量补充剂对维持性血液透析患者营养状态的影响

Public title:

Effect of energy supplementation on nutritional status in maintenance hemodialysis patients

注册题目简写:

English Acronym:

研究课题的正式科学名称:

能量补充剂对维持性血液透析患者营养状态的影响—— 一项多中心、随机、对照临床研究

Scientific title:

Effect of energy supplementation on nutritional status in maintenance hemodialysis patients: A multicenter, randomized, controlled clinical study.

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:

陈俊志 

研究负责人:

梁敏 

Applicant:

Junzhi Chen 

Study leader:

Min Liang 

申请注册联系人电话:

Applicant telephone:

+86 15920192127

研究负责人电话:

Study leader's
telephone:

+86 13076878921

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:

junzhichen2016@163.com

研究负责人电子邮件:

Study leader's E-mail:

nfyylm@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:

中国广东省广州市广州大道北1838号南方医院

研究负责人通讯地址:

中国广东省广州市广州大道北1838号南方医院

Applicant address:

1838 North Canton Road, Guangzhou, Guangdong, China

Study leader's address:

1838 North Canton Road, Guangzhou, Guangdong, China

申请注册联系人邮政编码:

Applicant postcode:

510515

研究负责人邮政编码:

Study leader's postcode:

510515

申请人所在单位:

中国广东省广州市南方医科大学南方医院肾内科

Applicant's institution:

Department of nephrology in Nanfang Hospital, Southern Medical University, Guangzhou, China

研究负责人所在单位:

中国广东省广州市南方医科大学南方医院肾内科

Affiliation of the Leader:

Department of nephrology in Nanfang Hospital, Southern Medical University, Guangzhou, China

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:

NFEC-2018-012

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:

南方医科大学南方医院伦理委员会

Name of the ethic committee:

Medical Ethics Committee of Nanfang Hospital, Southern Medical University

伦理委员会批准日期:

Date of approved by ethic committee:

2018-02-06 00:00:00

伦理委员会联系人:

胡兴媛

Contact Name of the ethic committee:

Xingyuan HU

伦理委员会联系地址:

中国广东省广州市广州大道北1838号南方医院

Contact Address of the ethic committee:

1838 North Canton Road, Guangzhou, Guangdong, China

伦理委员会联系人电话:

Contact phone of the ethic committee:

+86 020-62787238

伦理委员会联系人邮箱:

Contact email of the ethic committee:

nfyyec@163.com

研究实施负责(组长)单位:

中国广东省广州市南方医科大学南方医院肾内科

Primary sponsor:

Department of nephrology in Nanfang Hospital, Southern Medical University

研究实施负责(组长)单位地址:

中国广东省广州市广州大道北1838号南方医院

Primary sponsor's address:

1838 North Canton Road, Guangzhou, Guangdong, 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):

广东

市(区县):

广州

Country:

China

Province:

Guangdong

City:

Guangzhou

单位(医院):

南方医科大学南方医院

具体地址:

中国广东省广州市白云区

Institution
hospital:

NanFang Hospital,Southern Medical University

Address:

1838 North Canton Road, Guangzhou, Guangdong, China

经费或物资来源:

院级项目

Source(s) of funding:

Hospital-level project

研究疾病:

慢性肾脏病  

Target disease:

chronic kidney 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:

其它 

Study phase:

N/A

研究设计:

随机平行对照 

Study design:

Parallel 

研究目的:

主要研究目的: 在膳食能量摄入<30kcal/kg IBW/d的维持性血液透析患者中,与常规医学治疗相比,能量补充剂能够改善患者的营养状态。 次要研究目的: (1)在膳食能量摄入<30kcal/kg IBW/d的维持性血液透析患者中,与常规医学治疗相比,能量补充剂能够改善患者的生存质量。 (2)考察在膳食能量摄入<30kcal/kg IBW/d的维持性血液透析患者中,能量补充剂的安全性。  

Objectives of Study:

Primary Objective: Compared with the usual medical treatment, energy supplementation will improve the nutritional status in maintenance hemodialysis patients with dietary energy intake <30 kcal/kg IBW/day. Secondary Objectives: (1) Compared with the usual medical treatment, energy supplementation will improve the quality of life in maintenance hemodialysis patients with dietary energy intake <30 kcal/kg IBW/day; (2) To assess the safety of energy supplementation during the treatment in maintenance hemodialysis patients with dietary energy intake <30 kcal/kg IBW/day.

药物成份或治疗方案详述:

费瑞卡营养补充剂成分:不含有蛋白质、磷和钾,主要成分是脂肪(占总能量的96.8%),含有少量用于增甜的蔗糖维生素E、维生素K1和纤维素。 治疗方案: 治疗组:在正常饮食的基础上,每天给予1次60ml的费瑞卡营养补充剂(约300kcal),饭后口服使用,持续治疗12周。 对照组:给予常规的医疗处置 

Description for medicine or protocol of treatment in detail:

Fresubin ingrediant: The main ingredient is fat, which accounts for 96.8% of the total energy supplied. vitamin E, vitamin K1, dietary fiber and a small amount of sucrose for sweetening. Treatment programe: Treatment group:On the basis of normal diet, treatment group receives a dialy oral dose of 60ml Fresubin oral nutritional supplementation containing 300kcal energy after meal. Treatment lasts for 12 weeks. Controlled group:control group receives usual medical treatment. 

纳入标准:

Inclusion criteria

排除标准:

1.不能正常进食
2.有伴发疾病:甲状腺功能亢进、急性感染性疾病、糖尿病、肝硬
化、活动性自身免疫性疾病、肿瘤;
3.多器官功能衰竭;
4.在6个月内接受输注白蛋白治疗;
5.认知、沟通障碍,精神不稳定;
6.不能耐受口服营养补充剂或有使用营养补充剂的禁忌症;
7.研究者认为无法安全完成试验的任何情况。

Exclusion criteria:

1. Inability to eat properly;
2. Concomitant diseaseshyperthyroidism, acute infectious diseases, diabetes, cirrhosis, active autoimmune disease, cancer;
3. Multiple organ failure;
4. Received intravenous albumin treatment within the last 6 months;
5. Cognitive, communication disorder, mental instability;
6. Be allergic or intolerant to any ingredient found in the study product;
7. Subject is considered unsuitable for the study based on the study physician's assessment.

研究实施时间:

Study execute time:

From 2018-03-08 00:00:00 To 2019-07-01 00:00:00  

征募观察对象时间:

Recruiting time:

From 2018-03-08 00:00:00 To 2018-06-01 00:00:00

干预措施:

Interventions:

组别:

治疗组

样本量:

110

Group:

Traetment group

Sample size:

干预措施:

费瑞卡营养补充剂

干预措施代码:

Intervention:

Fresubin-Oral Nutritional Supplement

Intervention code:

组别:

对照组

样本量:

110

Group:

Controled group

Sample size:

干预措施:

常规医疗处置

干预措施代码:

Intervention:

General medical treatment

Intervention code:

研究实施地点:

Countries of recruitment and research settings:

国家:

中国

省(直辖市):

广东 

市(区县):

 

Country:

China

Province:

Guangdong

City:

单位(医院):

南方医科大学南方医院 

单位级别:

三级甲等 

Institution
hospital:

Nanfang Hospital, Southern Medical University

Level of the institution:

Tertiary A Hospital

国家:

中国

省(直辖市):

广东 

市(区县):

 

Country:

China

Province:

Guangdong

City:

单位(医院):

广州花都区人民医院 

单位级别:

三级甲等 

Institution
hospital:

Guangzhou Huadu District People’s Hospital

Level of the institution:

Tertiary A Hospital

国家:

中国

省(直辖市):

广东 

市(区县):

 

Country:

China

Province:

Guangdong

City:

单位(医院):

佛山市第一人民医院 

单位级别:

三级甲等 

Institution
hospital:

Foshan First People’s Hospital

Level of the institution:

Tertiary A Hospital

测量指标:

Outcomes:

指标中文名:

相位角

指标类型:

主要指标

Outcome:

Phase Angle

Type:

Primary indicator

测量时间点:

测量方法:

Measure time point of outcome:

Measure method:

指标中文名:

KDQOL-SF问卷

指标类型:

次要指标

Outcome:

KDQOL-SF questionnaire

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

使用后保存  

说明

Fate of sample:

Preservation after use  

Note:

征募研究对象情况:

Recruiting status:

正在进行

Recruiting

年龄范围:

Participant age:

最小 Min age 18 years
最大 Max age 79 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):

由秦献辉教授通过计算机软件产生随机序列

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

Random sequences was generated by Professor Xianhui Qin through computer software

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:

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):

公开原始数据日期:2019年1月;方式:数据存放于主要研究中心的数据管理系统,经主要研究者书面同意后分享

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

Date of sharing original data: January. 2019. Way of sharing: Data will be stored in a data management system at major research center and shared with the writen consent of principal investigator

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:

数据采集和管理使用基于FileMaker开发的EDC系统

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

Data collection and management uses an EDC system based on FileMaker

数据与安全监察委员会:

Data and Safety Monitoring Committee:

无/No

注册人:

Name of Registration:

 2018-03-06 12:26:58