Nutritional intervention
OtherDietary Counselling
NCT Number: NCT04066400
Effects of Wheat-based diet vs. ATI-free diet on NASH
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Notify Me18 year–75 year
All sexes
Interventional
Not applicable
Universität Frankfurt, Frankfurt, Germany
40 patients with the diagnosis of a non-alcoholic- steatohepatitis (NASH) will be recruited at the University Hospitals of Mainz and Frankfurt. Patients are assessed with regards to their diet using standardized questionnaire and nutritionists.
Patients will be randomized into two parallel groups. The first group will continue a wheat-based Nutrition, while the second Group will receive dietary counselling to achieve an ATI-free nutrition, trying to reduce the daily ATI consumption.
The clinical trial will run over 16 weeks including 4 visits at the study center. Study visits include physical examinations, blood-based parameters, cytokines and urine samples, as well for the analysis of the intestinal microbiome by using stool samples. In addition the patients have to complete dietary and health-related quality of life (HRQL) questionnaires. Visits are planned at baseline, W4, W8 and W16.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Dietary Counselling
Time frame: 16 weeks
Reduction of Alanine-Aminotransferase (ALT; U/ml) compared to baseline
Time frame: 16 weeks
The CLDQ is a validated patient-reported outcome measure
Johannes Gutenberg University Mainz
Other
Role of a Wheat-based Diet in NASH (NASH-ATI)
Acronym: NASH-ATI
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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