Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 9:57 PM
Ignite Modification Date:
2025-12-24 @ 9:57 PM
NCT ID:
NCT06032832
Eligibility Criteria:
Inclusion Criteria:
* Female aged between 18-45 y old
* Plasma ferritin \< 30 microgram/L
* BMI 18.5-25.0
* Weight \< 65 kg
* Signed informed consent
Exclusion Criteria:
* Anemic (Hb \< 12 g/dL)
* Inflammation (CRP \> 5 mg/L)
* Chronic digestive, renal and/or metabolic disease
* Chronic medications (except for oral contraceptives)
* Use of vitamin, mineral, and pre-and/or probiotic supplements in the previous 2 weeks and during the study
* Blood transfusion, blood donation, or significant blood loss (\> 400 ml) over the past 4 months
* Difficulty with blood withdrawal
* Antibiotic treatment in the 4 weeks preceding the start of the study and during the study
* Pregnancy (tested in serum at screening) or intention to become pregnant during the course of the study
* Lactation
* Earlier participation in a study using stable isotopes or participation in any clinical study within the last 30 days
* Participants who cannot be expected to comply with the study protocol (e.g. not available on certain study appointments)
* Inability to understand the information sheet and the informed consent form due to cognitive or language reasons
* Smoking
* celiac disease or gluten intolerance
* Vegetarian or vegan dietary regimen
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT06032832
Study Brief:
Protocol Section:
NCT06032832