Clinical study on the organ correlation in acute liver diseases

Not Applicable

Recruiting

• Conditions: iver diseases; Acute liver failure, acute on chronic liver diseases; D008107

• Registration Number: JPRN-jRCT1030230206
• Lead Sponsor: Kato Naoya

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2023-07-05
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

(1) Patients with liver disease who were admitted due to some exacerbating factor (liver failure, infection, hemorrhage, encephalopathy, ascites, dehydration, electrolyte abnormalities, etc.)
(2) Patients aged 18 years or older
(iii) Patients who have received a full explanation of the disease condition and treatment methods, have received an explanation of the study, and have obtained the free and voluntary written consent of the patient or a surrogate after full understanding of the study.

Exclusion Criteria

Patients deemed unsuitable as subjects by the study investigator or sub-investigator

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The frequency of cardiomyopathy, pulmonary hypertension, hepatopulmonary syndrome, and hepatorenal syndrome in ACLF and acute liver failure will be investigated, as well as their causes, risk factors and biomarkers for their development, and their subsequent clinical course.