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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ChiCTR
Last refreshed on: 15 July 2019
Main ID:  ChiCTR1900024411
Date of registration: 2019-07-10
Prospective Registration: No
Primary sponsor: Hu'nan Provincial People' Hospital
Public title: Effects of alternate-day fasting on body weight and dyslipidaemia in patients with non-alcoholic fatty liver disease
Scientific title: Effects of alternate-day fasting on body weight and dyslipidaemia in patients with non-alcoholic fatty liver disease
Date of first enrolment: 2018-08-01
Target sample size: Group A:95;Group B:95;Group C:95;
Recruitment status: Recruiting
URL:  http://www.chictr.org.cn/showproj.aspx?proj=39044
Study type:  Interventional study
Study design:  Parallel  
Phase:  New Treatment Measure Clinical Study
Countries of recruitment
China
Contacts
Name: Zhi-Yuan Chen   
Address:  61 Jiefang Road West, Changsha, Hu'nan, China 410005
Telephone: +86 0731 83928067
Email: chenzhiyuan@hunnu.edu.cn
Affiliation:  Department of Gastroenterology, Hu'nan Provincial People' Hospital
Name: Hua Cai,   
Address:  61 Jiefang Road West, Changsha, Hu'nan, China 410005
Telephone: +86 0731 83928069
Email: 965343605@qq.com
Affiliation:  Department of Gastroenterology, Hu'nan Provincial People' Hospital
Key inclusion & exclusion criteria
Inclusion criteria: BMI >24 kg/m2; age between 18 and 65 years; stable body weight for 3 months prior to the beginning of the study (<5 kg weight loss or weight gain)
Exclusion criteria: cardiovascular disease, uncontrolled hypertension, chronic inflammatory diseases, chronic infections, cancer, taking weight loss, lipid-, or glucose-lowering medications, and a history of bariatric surgery. Pregnant women and those planning a pregnancy or lactating

Age minimum: 18
Age maximum: 65
Gender: Both
Health Condition(s) or Problem(s) studied
non-alcoholic fatty liver disease
Intervention(s)
Group A:consumed 80% of their energy needs every day;Group B:????;Group C:Time-restricted feeding;
Primary Outcome(s)
Weight;
Secondary Outcome(s)
Secondary ID(s)
Source(s) of Monetary Support
No funding was obtained for this study
Secondary Sponsor(s)
Ethics review
Status: Approved
Approval date: 15/11/2018
Contact:
Jing-Shi Liu
Results
Results available:
Date Posted:
Date Completed:
URL:
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