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Completed

NCT Number: NCT04066400

Role of a Wheat Containing Diet on Non-alcoholic Steatohepatitis

Effects of Wheat-based diet vs. ATI-free diet on NASH

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Universität Frankfurt, Frankfurt, Germany

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • histologically proven NASH in the past 36 months with increased ALT: males: >60, females: >42 U/ml
  • no body weight modification about >10% in the past 24 weeks
  • no new drugs treating parts of the metabolic syndrome in the past 12 weeks
  • for patients with Diabetes: HbA1c value <8,6%
  • the ability to understand the aim and the possible individual consequences of this Trial
  • signed and dated consent before the Trial starts

Exclusion criteria

  • unstable coronary heart disease, stroke in the past 6 months
  • different liver diseases
  • proceeded fibrosis (Fibroscan >9,6 kPA) or histological cirrhosis
  • hepatocellular carcinoma or not curative treated carcinomas
  • alcohol consumption >10g/day (females), >20g/day (males)
  • gravidity
  • drugs causing secondary NASH (e.g. Tamoxifen, corticosteroids)
  • immunological or inflammatory diseases (e.g. systemic Lupus erythematodes)
  • warfarin therapy
  • implementation of another Special diet

Treatment and study plan

Nutritional intervention

Other

Dietary Counselling

Primary outcomes

  1. Effect of ATI-free Nutrition on hepatic inflammation

    Time frame: 16 weeks

    Reduction of Alanine-Aminotransferase (ALT; U/ml) compared to baseline

Secondary outcomes

  1. Quality of Life using the chronic liver disease questionnaire (CLDQ)

    Time frame: 16 weeks

    The CLDQ is a validated patient-reported outcome measure

Sponsors and collaborators

Lead sponsor

Johannes Gutenberg University Mainz

Other

Collaborators

  • Goethe University

Registry information

Official study title

Role of a Wheat-based Diet in NASH (NASH-ATI)

Acronym: NASH-ATI

Important dates

Study start
2018
Primary completion
2022
Study completion
2023
First posted
Aug 26, 2019
Registry last updated
Dec 28, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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