Phase
Condition
Inflammation
Treatment
Galactooligosaccharides (GOS)
Clinical Study ID
Ages 18-35 Female Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Female athlete.
Train at least 6 hours per week at moderate to high intensity.
Having low to moderate iron stores.
Willingness to consume the study supplement GOS during the intervention period.
Willingness not to consume daily nutritional supplements containing >20 mg ironand/or pre- or probiotics (excluding food and beverages containing live culturessuch as yoghurt, raw milk and cheese) during the study.
Willingness to not take any iron-containing supplements two days before and duringthe iron absorption study days or vitamin C on the iron absorption study days.
Exclusion
Exclusion Criteria:
Haemoglobin <11 g/dl.
Treated or self-reported chronic disease, malabsorptive or gastrointestinaldisorders (e.g. irritable bowel syndrome, functional bloating).
Pregnancy or lactation.
Subjects who cannot be expected to comply with the study protocol.
Difficulty drawing blood due to poor quality veins.
Individuals that have a fear of needles or suffer from vaso-vagal episodes whenexposed to blood.
Participants who plan to start or stop the use of contraceptives before or duringstudy period.
Participants who are lactose intolerant.
Participants who donated blood in the past 4 months or plan to donate during thestudy period.
Participants who use chronic anti-inflammatory medication such as corticosteroids ornon-steroidal anti-inflammatory medication (NSAIDS).
Study Design
Study Description
Connect with a study center
Este Vorster Research Facility
Potchefstroom, North West 2531
South AfricaSite Not Available
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