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 @ 1:06 PM
Ignite Modification Date:
2025-12-24 @ 1:06 PM
NCT ID:
NCT03625661
Eligibility Criteria:
Inclusion Criteria:
* Age ≥ 18 years
* Patient with cancer regardless of the location
* Patient with specific treatment (chemotherapy +/- targeted therapy and / or radiotherapy, hormone therapy or surgery)
* Patient with Functional Iron Deficiency or absolute with or without anemia
* Having given written informed consent prior to any procedure related to the study.
Exclusion Criteria:
* Patient in a palliative situation not receiving specific treatment for their cancer
* Patient is willing and able to comply with the protocol for the duration of the study including all scheduled treatment, visits and examinations
* Patient with myeloproliferative disease
* Contraindication to treatments for iron deficiency and / or anemia
* Pregnant woman, parturient or nursing mothers
* Patient has no valid health insurance
* Disorder precluding understanding of trial information or informed consent
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT03625661
Study Brief:
Protocol Section:
NCT03625661