Cirrhosis portal hypertension
Conditions
Interventions
control group:conventional treatment based on clinical experience
experimental group:real-time non-invasive pressure detection software portal pressure detection guides treatment
Sponsors
Shanghai Tongji Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: 1. Ages 18 to 70 years, regardless of gender; 2. Male or non-pregnant, non-lactating women; 3. The diagnosis of liver cirrhosis is confirmed by imaging, and the etiology of liver cirrhosis is not limited (viral hepatitis, autoimmune liver disease, fatty liver, alcoholic liver disease, genetic metabolic liver disease, etc.); 4. Unlimited stages of cirrhosis: compensatory period, decompensated period, late decompensated period; 5. Good cognitive ability and good compliance; 6. Agree to participate in this project and volunteer to sign the informed consent form;
Exclusion criteria
Exclusion criteria: 1. Patients with severe complications (hemorrhage of the digestive tract, liver coma, bacterial infection, hepatorenal syndrome, etc.) who are expected to survive less than six months; 2. Suspected or confirmed to have malignant tumor disease; 3. Language impaired; 4. People with a history of drug abuse and uncontrolled alcohol abuse; 5. Participated in other clinical trials within 3 months.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Complication rate;mortality rate; | — |
Countries
China
Contacts
Public ContactChangqing Yang
Shanghai Tongji Hospital
Outcome results
None listed