Skip to content

Clinical intervention study of resistant starch on the lipid metabolism of non-alcoholic fatty liver disease

Clinical intervention study of resistant starch on the lipid metabolism of non-alcoholic fatty liver disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-15007519
Enrollment
Unknown
Registered
2015-12-06
Start date
2016-03-01
Completion date
Unknown
Last updated
2021-12-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-alcoholic fatty liver disease

Interventions

Resistant starch group (RS):Resistant starch
Control starch group (CS):Control starch

Sponsors

Department of Endocrinology and Metabolism, Shanghai Jiao Tong University Affiliated Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Ethnic Chinese; 2. Liver steatosis diagnosed by ultrasonography; 3. Aged 18-70 years old; 4. Written informed consents must be obtained.

Exclusion criteria

Exclusion criteria: 1. Participants with diabetes mellitus 2. Participants with an alcohol consumption history of more than 20g per day for men and more than 10g per day for women 3. Participants with acute or chronic gastrointestinal diseases, malignant tumor or severe renal dysfunction 4. Pregnant, breastfeeding women or women planning to get pregnant 5. Participants using antibiotics within 3 weeks before or during the study 6. Participants with viral hepatitis, drug-induced liver disease, total parenteral nutrition, Wilson's disease, autoimmune liver disease and other specific diseases that can lead to fatty liver 7. Participants with routine use of prescription medicines or adjuvant Chinese and Western medicines (except regular contraceptives) 8. Participants expected to have poor compliance 9. Participants who have used weight loss medication or participated in weight-loss programs in the previous 3 months 10. Participants with mental disorders who cannot cooperate 11. Participants with pacemaker or metallic implants, claustrophobia or other conditions that would be unable to undergo magnetic resonance examinations

Design outcomes

Primary

MeasureTime frame
Change in intrahepatic triglyceride content (IHTC);

Secondary

MeasureTime frame
Change in anthropometric indicators;Change in body composition;Change in subcutaneous fat area (SFA);Change in visceral fat area (VFA);Glycemic control;Change in insulin sensitivity;Change in liver and renal function;Change in lipid profiles;Change in cytokines;Change in multi-omics parameters;Single nucleotide polymorphism (SNP);The remission rate of NAFLD;Percent change in intrahepatic triglyceride content;

Countries

China

Contacts

Public ContactWeiping Jia

Shanghai Jiao Tong University Affiliated Sixth People's Hospital

wpjia@sjtu.edu.cn+86 21 64369181

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 10, 2026