Natural Course and Prognosis of Hospitalized Patients With Cirrhosis

  • STATUS
    Recruiting
  • End date
    Oct 31, 2025
  • participants needed
    336
  • sponsor
    Kangbuk Samsung Hospital
Updated on 24 March 2022
ascites
carcinoma
encephalopathy
spontaneous bacterial peritonitis
hepatocellular carcinoma
hepatorenal syndrome

Summary

The aim of this prospective study is to evaluate the natural course and prognosis of hospitalized patients with liver cirrhosis.

Description

The aim of this prospective study is to collect data on hospitalized patients with liver cirrhosis at four institutions in Korea (Kangbuk Samsung Hospital, Hallym University Dongtan Sacred Heart Hospital, Chosun University Hospital, and National Medical Center). If patients agree to participate in this clinical trial, the patients' data (such as age, sex, height, weight, nutrition status [RFH-NPT], history of medication, laboratory findings, endoscopic findings, and radiologic findings) will be collected in a research database. The research database will be updated, every 6 months, to include data on patients' disease outcomes and follow-up care.

Details
Condition Liver Cirrhosis
Clinical Study IdentifierNCT05185154
SponsorKangbuk Samsung Hospital
Last Modified on24 March 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Hospitalized patients with liver cirrhosis
Admission to the hospital because of cirrhotic complications such as uncontrolled ascites, variceal bleeding, hepatic encephalopathy, hepatorenal syndrome, spontaneous bacterial peritonitis, hepatocellular carcinoma, acute kidney injury, bacterial infection, acute liver failure, and etc

Exclusion Criteria

Admission to the hospital without cirrhotic complications
Patients who refuse the follow-up of outpatient department
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How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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