Ireland
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Enrolling by invitation Not applicable

The Impact of a Dietary Fiber Enriched Diet on the Outcome of Patients with Liver Cirrhosis

NCT06634186 · tracked via the Priya Life Science Germany tracker
Phase
Not applicable
Started
2023-01-23
Last updated
2024-10-09

Condition(s) studied

Liver Cirrhosis

Investigational drug(s) / intervention(s)

Dietary intervention

Dietary intervention: The aim of the dietary intervention is the implementation of a fiber-enriched diet. Therefore, patients receive dietary counseling, supplemented with propionate, that functions as fiber-surrogate.

Study summary

The goal of this dietary intervention is to study the impact of a dietary fiber enriched diet on the intestinal dysbiosis, systemic inflammation and cirrhosis-related complications in patients with liver cirrhosis.

Therefore, our aim is to investigate the impact of a dietary fiber enriched diet on

* frailty and sarcopenia
* systemic inflammation
* microbiome composition
* quality of life and the composition of patients diet.

Participants receive a dietary counselling and will be asked to increase their dietary fiber intake. As malnutrition is a common complication in cirrhosis and patients with advanced liver disease often show a disability to meet their daily food-requirements, the recommended intake of 30 gram dietary fibers per day is unlikely in this group of patients. Therefore, the fiber-enriched diet will be supplemented by the physiological short-chain-fatty-acid propionate, as a fiber-surrogate.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients of legal age and with the ability to give informed consent * Patients with liver cirrhosis and portal hypertension Exclusion Criteria: * Patients with transjugular intrahepatic portosystemic shunt (TIPS) * significant immunosuppression * malignant tumor * underage

Primary outcome measure(s)

  • Change of the Liver Frailty Index — The Liver Frailty Index will be measured at each study visit (Baseline, after 2 month and after 5 month)

Trial sites (1)

FacilityCityRegionStatus
Hannover Medical School (MHH) Hanover Lower Saxony
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06634186 on ClinicalTrials.gov ↗ ← All trials in Germany