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:
2026-03-26 @ 3:17 PM
Ignite Modification Date:
2026-03-26 @ 3:17 PM
NCT ID:
NCT07308769
Eligibility Criteria:
Inclusion Criteria:
* Female participants ≥ 18 years
* Mild anemia (11.0 ≤ Hb \< 12 g/dL) or moderate anemia (8.0 \< Hb \< 11 g/dL)
* Signed informed consent
Exclusion Criteria:
* Use of iron-containing drugs or supplements within 1 month prior to screening
* Psychiatric disorders interfering with consent or compliance
* Active cancer (except fibroids and polyps)
* Pregnant or breastfeeding women
* Participation in another interventional study
* History of poor adherence or inability to comply
* Use of erythropoietin within 3 months prior to screening
* Need for blood transfusion or IV iron (per investigator judgment)
* Severe active IBD (HBI \> 16 for Crohn; CAI \> 12 for ulcerative colitis)
* Previous bariatric surgery
* Alcohol abuse
* Hemochromatosis or iron overload syndromes
* Hereditary anemias (including thalassemia)
* Known hypersensitivity to study product ingredients
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT07308769
Study Brief:
Protocol Section:
NCT07308769