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Zinc Absorption in Flakes Derived from Sprouted or Hydrothermally Processed Wheat (Wheatflakes)

C

Catholic University (KU) of Leuven

Status

Completed

Conditions

Zinc Absorption

Treatments

Dietary Supplement: Processing of wheat

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The aim of this project is to investigate whether the increased zinc bio-accessibility values in sprouted or hydrothermally processed wheat is reflected in an increased zinc absorption in human subjects after consuming breakfast flakes derived from such processed wheats.

Full description

The zinc study is a randomised crossover design with two different meals (control wheat flakes and flakes derived from sprouted wheat or flakes derived from hydrothermally processed wheat) spiked with a specific zinc isotope. The study contains two test groups (I and II) of 26 and 10 participants, respectively. Both test groups will consume the control wheat flakes, whereas test group I will consume the flakes from sprouted wheat and group II the flakes from hydrothermally processed wheat randomised over two test days. An intravenous dose of Zn will be given on day 1 of the study and the zinc isotope composition in the urine of the participants will be measured on day 1,5,6,7 and 8 of the study.

Enrollment

34 patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • BMI range 18.5-25.0 kg/m²
  • Regular diet with 3 meals a day (at least 5 times a week)

Exclusion criteria

  • Intake of vitamin and/or mineral supplements during and 2 weeks before the stud
  • Intake of antibiotics 3 months prior to the study
  • Intake of medicines that have an impact on the gastrointestinal tract during and 2 weeks before the study
  • Previous or current gastrointestinal (e.g. Crohn's disease), endocrine or eating disorders or other gastrointestinal history
  • Previous or current substance/alcohol dependence or abuse (> 2 units per day/14 units per week)
  • Currently smoking (have smoked in the last 28 days) or willingness to smoke during the study period
  • Pregnant or lactating or wishing to become pregnant in the period of the study
  • Allergy or intolerance to wheat (coeliac disease, gluten sensitivity) or citric acid
  • Adherence to vegan or vegetarian diets or special diets (weight loss, gluten-free etc...)
  • Blood donation in the 6 months prior to the study

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

34 participants in 3 patient groups

Control wheat flakes
Active Comparator group
Description:
Wheat flakes made of whole derived from unprocessed wheat
Treatment:
Dietary Supplement: Processing of wheat
Flakes from sprouted wheat
Active Comparator group
Description:
Wheat flakes made of whole derived from sprouted wheat
Treatment:
Dietary Supplement: Processing of wheat
Flakes from hydrothermally processed wheat
Active Comparator group
Description:
Wheat flakes made of whole derived from hydrothermally processed wheat
Treatment:
Dietary Supplement: Processing of wheat

Trial contacts and locations

1

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Central trial contact

Kristin Verbeke, Prof.; Marie Huyskens, MSc

Data sourced from clinicaltrials.gov

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