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Study on obtaining T1-related quantitative mapping of abdominal magnetic resonance imaging in chronic liver disease under free-breathing

Study on obtaining T1-related quantitative mapping of abdominal magnetic resonance imaging in chronic liver disease under free-breathing

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500108591
Enrollment
Unknown
Registered
2025-09-02
Start date
2025-09-02
Completion date
Unknown
Last updated
2025-09-08

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

Conditions

Chronic liver disease

Interventions

Fatty liver disease observation group:None
Healthy control group:None

Sponsors

Shanghai Municipal Hospital of Traditional Chinese Medicine;Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria for subjects with fatty liver disease: Attended the fatty liver disease clinic of Shanghai Hospital of Traditional Chinese Medicine and Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, according to the 2023 international clinical diagnostic criteria [A multi-society Delphi consensus statement on new fatty liver disease nomenclature. Hepatology.2023; 78(6):1966-1986], diagnosed with CLD (SLD) by imaging or prior pathology , agreeing to undergo blood tests and MRI examinations. If willing to undergo liver biopsy, MRI scan and blood tests are performed within 3 days prior to biopsy. Inclusion criteria for healthy volunteers: meet the basic inclusion criteria, no history and clinical symptoms of chronic liver disease (fatty liver, hepatitis, cirrhosis); Normal liver function; Abdominal MRI-PDFF showed liver fat content <5%; No history of long-term alcohol consumption; No use of drugs affecting liver metabolism in the past 6 months; Voluntarily sign the informed consent form

Exclusion criteria

Exclusion criteria: Those who cannot cooperate with or tolerate the examination; Subjects with contraindications to MRI examination and factors affecting image quality; Subjects with mental illness, oncological disease, or severe cardiovascular disease; Pregnant women; No blood test results; Large space-occupying lesions in the liver (long axis diameter > 20mm); Malignancy; renal insufficiency, glomerular filtration rate less than 60 ml/min×1.73m^2; cardiac insufficiency.

Design outcomes

Primary

MeasureTime frame
T1 value;R2* value;Proton density fat fraction;Arterial blood flow;Portal vein blood flow;Total blood flow;Arterial fraction;The volume of distribution of the Gd contrast agent through the hepatic compartment;The average time from arterial or portal vein intake through the liver to venous output to venous output;Classification of hepatic steatosis;Iron deposition;Ishak score;METAVIR score;Hemoglobin;Platelet count;Routine coagulation;Total protein;Prealbumin;Alanine aminotransferase;Aspartate aminotransferase;Alkaline phosphatase;?-Glutamyl Transpeptidase;Hyaluronidase;Laminin;Human type III procollagen;Type IV procollagen peptide;Total cholesterol;Triglycerides;High-density lipoprotein;LDL;QSM value;

Countries

China

Contacts

Public ContactYang Shuohui;Lu Fang

Shanghai Municipal Hospital of Traditional Chinese Medicine;Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine

caddie_yang1980@aliyun.com+86 21 5663 9828

Outcome results

None listed

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