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The Effects of Dietary Supplements on Glycemic Control, Body Composition and Hepatic Fat Content in People With Prediabetes

The Effects of Dietary Supplements on Glycemic Control, Body Composition and Hepatic Fat Content in People With Prediabetes

Recruiting
40-80 years
All
Phase N/A

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Overview

This clinical study aims to explore the effects of 3 dietary supplements on metabolic parameters, liver fat content, and body composition in individuals with prediabetes. Prediabetes refers to a condition where blood sugar levels are higher than normal but not high enough for a diabetes diagnosis. The study will last for three months, during which participants will either take a dietary supplement or a placebo. Five groups will be studied, including placebo groups. Blood tests will assess glucose and lipid metabolism parameters, adipokines, and liver and kidney function. Liver stiffness and fat content will also be measured using elastography. Additionally, body composition will be assessed, and participants' psychological state, quality of life, eating habits and sports habits will be evaluated using questionnaires.

Eligibility

Inclusion Criteria:

  • willingness and ability to provide written informed consent and comply with all study requirements,
  • age between 40 and 80 years
  • prediabetes with a HbA1c level between 5,7-6,4%
  • no antidiabetic treatment prior to the inclusion in the study
  • BMI between 25 and 35 kg/m2
  • fasting glucose of 100-125mg/dl
  • in the case of women of childbearing potential, providing a negative pregnancy test at inclusion and once a month until the end of the study

Exclusion Criteria:

  • failure to provide written informed consent and/or failure to comply with the study requirements
  • age <40 years
  • HbA1c outside of the set range
  • significant impairments of hepatic and/or renal function
  • clinically significant abnormalities in medical history, routine laboratory screening, or in physical examination
  • allergies against any of the components of the dietary supplements or the placebo
  • type 1 diabetes mellitus, latent autoimmune diabetes in adults, maturity-onset diabetes of the young, gestational diabetes
  • pregnancy, lactation
  • concurrent treatment with any antidiabetic drug
  • concurrent treatment with drugs/dietary supplements that have proven interactions with dietary supplements included in our study

Study details
    PreDiabetes

NCT06437938

Medical University of Vienna

8 June 2024

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FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

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Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

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Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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