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:
2025-12-25 @ 4:07 AM
Ignite Modification Date:
2025-12-25 @ 4:07 AM
NCT ID:
NCT01521520
Eligibility Criteria:
Inclusion Criteria:
* Participation in a collaborating diabetes clinical trial
* Able to understand written consent document and HIPAA authorization prior to initiation of study related procedures and are willing to participate
Exclusion Criteria:
* Known allergy to ferumoxytol or iron
* Individuals who are pregnant or lactating
* Iron saturation above the upper limit of normal
* Individuals with a counter-indication to MRI, such as the presence of metallic prostheses or implanted metal device (e.g., infusion pump, defibrillator)
* Individuals with known clinical conditions that may lead to iron overload including hemochromatosis, cirrhosis, or sickle cell disease
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT01521520
Study Brief:
Protocol Section:
NCT01521520