Actively Recruiting
Real World Study of End-stage Liver Disease in China
Led by Huashan Hospital · Updated on 2019-07-30
10000
Participants Needed
1
Research Sites
521 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The aims of this study are exploring the current situation of end-stage liver disease in China, and the optimization of diagnosis and treatment. Liver cirrhosis often accompanied by a series of complications. Therefore, it is necessary to standardize the diagnosis and treatment of liver cirrhosis and its complications. End-stage liver disease mainly refers to the late stage of liver disease caused by various chronic liver damage. Its main feature is that liver function can not meet the physiological needs of human body. This study is a single-center, prospective and observational real-world study aimed at investigating and analyzing the current diagnosis and treatment of liver cirrhosis and end-stage liver disease in China.
CONDITIONS
Official Title
Real World Study of End-stage Liver Disease in China
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients must give informed consent.
- Diagnosis of acute decompensation of cirrhosis, chronic and acute liver failure, chronic liver failure, or hepatocellular carcinoma (stage III-IV).
You will not qualify if you...
- HIV positive or AIDS patients.
- History of serious psychiatric illness, including major depression, psychosis, suicide attempts, hospitalization due to mental illness, or disability from mental illness.
- Serious diseases affecting heart, lung, kidney, brain, blood, or other important organs.
- Presence of other malignant tumors except those cured.
- Pregnant, breastfeeding, or women of childbearing age planning to conceive.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
HuaShan Hospital
Shanghai, Shanghai Municipality, China, 200040
Actively Recruiting
Research Team
J
Jingwen Ai, Doctor
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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