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Analysis on Characteristics of Hepatic Metabolic Response to Diet and Circadian Rhythm and Exploration of Therapeutic Targets

Analysis on Characteristics of Hepatic Metabolic Response to Diet and Circadian Rhythm and Exploration of Therapeutic Targets

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600126390
Enrollment
Unknown
Registered
2026-06-08
Start date
2026-06-17
Completion date
Unknown
Last updated
2026-06-15

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

Conditions

Obesity and MASLD

Interventions

Normal+High-glucose meal:High-glucose meal
Normal+High-protein meal:High-protein meal
Normal+High-fat meal:High-fat meal
Normal+Mixed meal:Mixed meal
Overweight+High-glucose meal:High-glucose meal
Overweight+High-protein meal:High-protein meal
Overweight+High-fat meal:High-fat meal
Overweight+Mixed meal:Mixed meal

Sponsors

Shandong Provincial Hospital Affiliated to Shandong First Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 20 and 70 years, inclusive (20 = age = 70); 2. Good compliance, ability to complete electronic questionnaires using a smartphone, and willingness to undergo biological sample collection; 3. Complete clinical examination and laboratory test data, and meeting the predefined eligibility criteria; 4. Agreement to comply with the study requirements during the study period, accept the dietary intervention provided by the research team, and provide blood samples.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating women; 2. Individuals who have undergone surgery under general anesthesia within the past 3 months; 3. Individuals with a history of substance dependence according to DSM-5 criteria, including tobacco consumption of more than 20 cigarettes per day; 4. Individuals with known neurological, psychiatric, or systemic diseases that may affect cognitive function, including head trauma, subdural hematoma, current depression, and epilepsy; 5. Individuals with any other disease or major systemic condition that, in the investigator’s judgment, may affect study participation or outcome assessment, such as chronic kidney disease, heart disease, or chronic respiratory failure; 6. Individuals with strong pre-existing dietary preferences, special dietary requirements such as vegetarianism, or allergy to any food component used in the study; 7. Individuals who voluntarily withdraw from the study for subjective or objective reasons.

Design outcomes

Primary

MeasureTime frame
Insulin + C-peptide (fasting and postprandial);Blood glucose;

Secondary

MeasureTime frame
HbA1c;Hepatic function;Renal function;Blood omics analysis;Serum lipid profile;Serum uric acid;Blood routine;Blood pressure;Pulse rate;Height;Body weight;Chest circumference;Waist circumference;Hip circumference;Neck circumference;Body composition analysis;Ultrasonography;FibroScan;

Countries

China

Contacts

Public ContactYao Zhenyu

Shandong Provincial Hospital Affiliated to Shandong First Medical University

yaozhenyu@sdfmu.edu.cn+86 187 6978 1076

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 21, 2026