Prognostic potential of different tests for liver function in patients with cirrhosis

Recruiting

• Conditions: K71.9; K72.1; Toxic liver disease, unspecified; Chronic hepatic failure

• Registration Number: DRKS00000614
• Lead Sponsor: Klinik für Allgemein-, Viszerall- und Transplantationsmedizin

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2012-06-14
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 300

Inclusion Criteria

1. patients with liver cirrhosis fulfilling Child b or c
2. 18-75 years old, both sex
3. patients which signed the informed consent

Exclusion Criteria

1. patients listed for other than liver transplantation
2. acute liver failure
3. patients with sver infectious disease
4. uncompliance

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
status of the patient: death, liver transplantation, or survival without transplantation at timepoints 6,12, and 24 moths will be prooven via telephone contact with the patient.

Secondary Outcome Measures

Name	Time	Method
Changes of quality of life by means of COLQ- German version and occurence of complications related to cirrhosis will be evaluated on timepoint 0 and after 6, 12 and 24 month respectively using telephon follow up calls. Acquired data will be documented in special designed clinical report forms.