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The diagnostic model for MAFLD based on non-invasive biomarkers in volatile organic compounds (VOCs) metabolomic profiling

The diagnostic model for MAFLD based on non-invasive biomarkers in volatile organic compounds (VOCs) metabolomic profiling

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300078480
Enrollment
Unknown
Registered
2023-12-11
Start date
2023-12-11
Completion date
Unknown
Last updated
2023-12-19

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

Conditions

metabolic dysfunction-associated fatty liver disease

Interventions

Dietary intervention group:The patients in this group were given a light vegetarian diet intervention, and pictures were taken before and after three meals, and the specific diet types were described
Fruits (except durian, mango, lychee, etc.)
Daily can drink porridge: millet based, Job's tears, red bean porridge, 1 ~ 2 times a day
Exercise intervention group:Exercise intervention was performed in this group of patients, and video recording was performed for archiving. Exercise strictly in accordance with the following exercise
Diet and exercise combined intervention group:In this group of patients, light vegetarian diet intervention and exercise intervention were carried out simultaneously. The diet pattern and exercise pre
Healthy control group:No special intervention for patients
Healthy group on time-restricted diet alone:Eating time is set within 8 hours per day, and there is no restriction on food types

Sponsors

China-Japan Friendship Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) patients with the diagnostic criteria of MAFLD (2) patients at age 18-65; (3) individuals with body mass index (BMI) between 18.5 and 35; (4) Volunteer to participate in the study and sign the informed consent

Exclusion criteria

Exclusion criteria: (1) Patients who have progressed to the decompensated stage of cirrhosis; (2) Women in the pregnancy or breastfeeding period, allergic people; (3) Patients with other serious brain, heart, lung, kidney, blood system, connective tissue and muscle system, malignant tumor diseases and mental diseases in addition to hypertension, diabetes, hyperlipidemia; (4) Patients with severe metabolic disorders, including uncontrolled hypertension (diastolic blood pressure =100 mmHg or systolic blood pressure =180 mmHg), type I diabetes mellitus, type II diabetes mellitus with brain, eye, kidney complications, type II diabetes mellitus with poor blood glucose control and HBA1c > 10%; (5) People who have used any other drug within 3 months that affects liver function, causes hepatic steatosis, or may have an impact on this study (including tamoxifen, ethamiodarone, sodium valproate, methotrexate, glucocorticoids, probiotics, amiodarone, olazepine).

Design outcomes

Primary

MeasureTime frame
HFC;liver function;Blood lipid;Weight change;

Secondary

MeasureTime frame
Waist circumference;blood sugar;blood pressure;hs-CRP;Oxidative stress indicators;

Countries

CHINA

Contacts

Public ContactShukun Yao

Department of Gastroenterology, China-Japan Friendship Hospital, Beijing, China

shukunyao@126.com+86 135 0100 8676

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026