A clinical study of mixed reality technology (MR) in the selection of precise surgical protocols for cirrhotic patients with portal hypertension

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2500098907

Enrollment

Unknown

Registered

2025-03-14

Start date

2025-03-22

Completion date

Unknown

Last updated

2025-03-17

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

Conditions

Cirrhotic portal hypertension

Interventions

Observation Group:none

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Patients aged 18-80 years old; 2.Diagnosed with portal hypertension of liver cirrhosis; 3.HVPG or FPP measurement is successful;

Exclusion criteria

Exclusion criteria: 1.Pregnant or lactating patients; 2.Patients with severe abnormality of coagulation function, heart function and lung function or poor general condition; 3.Patients with iodine allergy;

Design outcomes

Primary

Measure	Time frame
HVPG or FPP predicted value and standard value;	—

Countries

China

Contacts

Public ContactLei Zheng

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

zl1055174020@163.com+86 150 0002 2831

Outcome results

None listed

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