Eligibility Module

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 @ 10:59 PM
Ignite Modification Date: 2025-12-24 @ 10:59 PM
NCT ID: NCT02683369
Eligibility Criteria: Inclusion Criteria: 1. Pre-menopausal 2. Iron deficient without anemia (serum ferritin concentration \< 20 ug/L and a hemoglobin concentration \> 120 g/L) 3. Agree to continue with current diet and any dietary supplements 4. Able to understand and write English 5. Voluntarily consent to the study and understand its nature and purpose including potential risks and side effects Exclusion Criteria: 1. Daily supplementation of another iron supplement (other than multivitamin) currently or within past 2 weeks 2. Pregnant or breastfeeding females 3. History of alcohol, drug, or medication abuse 4. Known allergies to any substance in the study product 5. Donated blood in the past month or plan to do so at any time during the 8-week trial 6. Current diagnosis of inflammatory bowel disease (Crohn's or Ulcerative Colitis) 7. Taking medication that my interfere with the absorption of iron 8. Current tobacco smoker
Healthy Volunteers: True
Sex: FEMALE
Minimum Age: 18 Years
Maximum Age: 55 Years
Study: NCT02683369
Study Brief:
Protocol Section: NCT02683369