MedPath

utritional Intervention before liver transpantation (LTx)

Not Applicable
Recruiting
Conditions
Z75.67
Registration Number
DRKS00023353
Lead Sponsor
Medizinische Klinik und Poliklinik IIKlinikum der Universität München
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
125
Inclusion Criteria

listed to liver transplantation on the basis of liver cirrhosis / oral or enteral nutrition / adults / the written informed consent

Exclusion Criteria

Intolerance to oral supplements / only parenteral nutrition possible / patients with a pacemaker (KI for BIA measurement) / minor patients / people who are temporarily or permanently unable to give their consent / pregnant patients / patients requiring intensive care

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<br>Increase in the phase angle in the bioelectrical impedance measurement (BIA measurement) by 20% after 12 weeks
Secondary Outcome Measures
NameTimeMethod
- Increase in hand strength - Improvement of the 6 min walking test - Biochemical parameters (albumin, total protein) - Less frequent hospital stays during the waiting period and shorter hospitilation during transplantation - Improvement in quality of life and nutritional status (PG-SGA score) - Measurement of the skeletal muscle index in the context of radiological tomography to assess sarcopenia over the course - lower mortality<br>
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