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 @ 9:54 PM
Ignite Modification Date:
2025-12-24 @ 9:54 PM
NCT ID:
NCT01634932
Eligibility Criteria:
Inclusion Criteria:
* Females of reproductive age, 18-30 years
* Low/marginal iron status (Hb \> 9.0 g/dl, SF \< 25 ;g/L)
* Maximum body weight 65 kg
* Normal body mass index (18.5-25 kg/m2)
* Obtained consent
Exclusion Criteria:
* Pregnancy or Lactating (assessed by pregnancy test)
* Fever (body temperature \>37.5 °C)
* Symptomatic malaria infection (positive blood smear for Plasmodium species + symptoms)
* Infection with soil-transmitted helminthes (positive stool samples and/or urine samples)
* Intake of mineral/vitamin supplements 2 weeks before and during the study
* Metabolic or gastrointestinal disorders, eating disorders or food allergy
* Regular intake of medication
* Blood transfusion, blood donation or significant blood loss (accident, surgery) over the past 6 months
* Currently participating in another clinical trial or having participated in another clinical trial during the last 3 months prior to the beginning of this study
* Former participation in a study involving administration of iron stable isotopes
* Subject who cannot be expected to comply with study protocol
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
30 Years
Study:
NCT01634932
Study Brief:
Protocol Section:
NCT01634932