A Study to Predict Recompensation in Patients With Decompensated Cirrhosis Using Spleen Stiffness and Simple Blood Tests

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-75
SponsorBeijing Friendship Hospital

About this trial

The goal of this observational study is to learn if spleen stiffness and other non-invasive markers can help predict recompensation in people with decompensated cirrhosis who are receiving effective treatment for the cause of their liver disease. The main questions it aims to answer are:

* Can spleen stiffness and blood test results predict who will get better and stay better after cirrhosis becomes worse? * What are the features of people who recover after decompensation?

Participants will:

* Be people with decompensated cirrhosis who are already getting effective treatment (such as antiviral therapy or alcohol abstinence) * Be followed over time to check if they remain stable or have more liver problems * Have non-invasive tests done, including spleen stiffness measurement and blood tests

Researchers will track how many participants recover and stay recovered over time, and use that information to build a tool to help predict outcomes in others with cirrhosis.

Eligibility criteria

Qualifiers

Male or female, aged 18 to 75 years (inclusive)

Clinically diagnosed decompensated cirrhosis

First decompensated event occurred within 12 months of screening, or no decompensated events in the past 12 months despite a history of decompensation

For HBV: Sustained antiviral suppression

Disqualifiers

Missing data on first decompensated event

Prior orthotopic liver transplantation or TIPS

Prior splenectomy, splenic embolization, or other shunt surgery

History or current diagnosis of hepatocellular carcinoma

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

735 Participants
are grouped into 2 trial groups

Sponsors and collaborators