Skip to content

A non-invasive diagnosis system for liver inflammation was established based on the LivQ-box® parameters of iLivTouch

A non-invasive diagnosis system for liver inflammation was established based on the LivQ-box® parameters of iLivTouch

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500111891
Enrollment
Unknown
Registered
2025-11-07
Start date
2025-11-13
Completion date
Unknown
Last updated
2025-11-11

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

Conditions

Chronic liver inflammation (chronic hepatitis B, fatty hepatitis)

Interventions

Gold Standard:Liver biopsy was performed to evaluate liver inflammation according to the GS scoring system, the Metavir scoring system and the Ishak scoring system.

Sponsors

Beijing Friendship Hospital Affiliated to Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Retrospective 1. Age 18 years or older, any gender; 2. Patients with a history of liver biopsy-confirmed chronic liver inflammation (chronic hepatitis B, steatohepatitis), and for whom liver biopsy specimens or pathology images/reports are available; 3. Patients who underwent iLivTouch examination within +/-7 days of the liver biopsy, with results that can be exported; 4. Patients for whom demographic, biochemical, and etiological information within 7 days before and after the liver biopsy is available. Prospective: 1. Age 18 years or older, any gender; 2. Clinically diagnosed with chronic hepatitis and agree to undergo liver biopsy and concurrent iLivTouch examination (interval <+/-7 days); 3. Voluntarily sign a written informed consent form.

Exclusion criteria

Exclusion criteria: Retrospective: 1. Combined with other chronic liver diseases (drug-induced liver injury, alcoholic liver disease, autoimmune liver disease, genetic metabolic liver disease, etc., excluding fatty liver); 2. Use of drugs within one month that may directly affect liver function test indicators (such as bicyclol, polyene phosphatidylcholine, Schisandra-containing traditional Chinese medicine, silymarin, glycyrrhizin, etc.); 3. Patients with more than 50% missing demographic, biochemical, or etiological information. Prospective: 1. Patients with hepatic conditions involving significant deposition of abnormal substances other than fat and collagen, such as obstructive bile duct disease, cholestatic liver disease, and inherited metabolic liver diseases; 2. Patients who have taken medications within the past month that may directly affect liver function test indicators (such as bifendate, Wuzi capsule, traditional Chinese medicine containing Schisandra, silymarin compounds, glycyrrhizin derivatives, polyunsaturated phosphatidylcholine, etc.); 3. Patients with unresolved wounds or scars in the right upper abdomen that make ultrasound examination inappropriate; 4. Any contraindications to liver puncture, including but not limited to: (1) clinical consideration of hepatic hemangioma or multilocular echinococcosis; (2) extrahepatic obstructive jaundice; (3) significant bleeding tendency, or severe thrombocytopenia or coagulation disorders; (4) coma or uncooperative due to other diseases; (5) infection along the puncture path. 5. Any contraindications to iLivTouch, including but not limited to active infection in the right upper abdomen, pregnancy, etc.; 6. Patients with severe diseases of major organs such as the heart, lungs, kidneys, brain, or hematologic system; 7. Patients with severe mental illnesses (such as depression, mania, schizophrenia, etc.); 8. Pregnant and breastfeeding women; 9. Patients deemed by the investigators as unsuitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
Specificity;Clinical diagnostic threshold;

Countries

China

Contacts

Public ContactWu Xiaoning

Beijing Friendship Hospital Affiliated to Capital Medical University

wuxiaoningbs@126.com+86 10 63138665

Outcome results

None listed

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