Clinical Study on Non-invasive Assessment of Portal Hypertension in Patients with Liver Cirrhosis Assisted by Artificial Intelligence Multimodal Models

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2600117744

Enrollment

Unknown

Registered

2026-01-28

Start date

2026-02-01

Completion date

Unknown

Last updated

2026-02-02

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

Conditions

Portal Hypertension

Interventions

Observational group:None

Eligibility

Sex/Gender

All

Age

18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1.Patients aged > 18 years and <= 85 years. 2.Patients diagnosed with liver cirrhosis.

Exclusion criteria

Exclusion criteria: 1.Pregnant or lactating patients. 2.Patients with severe abnormalities of coagulation function, cardiac function, or pulmonary function, or those in poor general condition. 3.Patients with iodine allergy.

Design outcomes

Primary

Measure	Time frame
Measurement value of hepatic venous pressure gradient (HVPG);Artificial intelligence multimodal model assisted non-invasive HVPG measurement values;	—

Secondary

Measure	Time frame
Liver stiffness measurement (Fibroscan;	—

Countries

China

Contacts

Public ContactZheng Lei

Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine

zl1055174020@163.com+86 15000022831

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026