Actively Recruiting

Phase Not Applicable
Age: 18Years - 100Years
All Genders
Healthy Volunteers
NCT03080129

Microbiome and Sarcopenia in Patients With Liver Cirrhosis

Led by Medical University of Graz · Updated on 2024-10-09

120

Participants Needed

1

Research Sites

503 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Protein-energy malnutrition (PEM) occurs in 65-90% of patients with liver cirrhosis. Severity of malnutrition correlates with progression of liver disease and leads to sarcopenia in 30-70% of cirrhotic patients. Malnutrition and sarcopenia are associated with an increased risk of complications and mortality. In cirrhosis the gut microbiome is altered leading to increased gut permeability, bacterial translocation and inflammation. Since the microbiome is involved in nutrient uptake and metabolism, it is hypothesized that microbiome alterations contribute to sarcopenia. A prospective controlled cohort study to investigate the interrelation of microbiome changes and sarcopenia in cirrhosis will be conducted. Furthermore the effect of nutritional interventions on the microbiome in cirrhosis will be studied. From this study information on how the gut microbiome composition and sarcopenia are associated in cirrhosis and if modulation of the gut microbiome by nutritional interventions is feasible will be collected.

CONDITIONS

Official Title

Microbiome and Sarcopenia in Patients With Liver Cirrhosis

Who Can Participate

Age: 18Years - 100Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Hospitalized patients for any reason with clinical, radiological, or histological diagnosis of cirrhosis
  • Age over 18 years
  • Able to provide informed consent
  • CT or MRI scan performed within 14 days before or after the baseline study visit
Not Eligible

You will not qualify if you...

  • Hepatic encephalopathy above grade 2 or other cognitive disorders preventing informed consent
  • Advanced hepatocellular carcinoma
  • Any condition or circumstance that may affect the patient's ability to participate in the study, as judged by the investigator

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Medical University Graz

Graz, Austria

Actively Recruiting

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Research Team

V

Vanessa Stadlbauer-Köllner, AssocProf Dr

CONTACT

J

Julia Haberl, BSc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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