Iron deficiency in cancer: a hidden problem exposed
NCT ID NCT01968304
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at how common iron deficiency is in cancer patients starting chemotherapy. Researchers checked iron levels in 480 adults with solid tumors or lymphoma. The goal was to find out how many patients might benefit from iron injections, without using other drugs like erythropoietin. The study did not test a treatment, but aimed to better understand iron needs during cancer care.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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480 people
The number who actually took part.
- Start date
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Sep 2013
- Finished
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Apr 2016
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Patients aged over 18 years of age. 2. Patients with a locally advanced or metastatic solid cancer (breast, colorectal, prostate, ENT, and lung) scheduled to receive first-line chemotherapy for metastatic disease or Patients with a lymphoma-type hematologic cancer scheduled for first-line chemotherapy 3. Patients who have read the information leaflet and have signed the informed consent. 4. Patients covered by national medical insurance. Exclusion Criteria: 1. Patients currently undergoing chemotherapy 2. Patients with diagnosed ID 3. Patients having received oral iron or injectable iron treatment during the previous 3 months 4. Patients receiving EPO or transfused during the 3 months prior to inclusion. 5. Patients unable to give their consent. 6. Patients over 18 but under guardianship or public guardianship. 7. Vulnerable individuals as defined by article L1121-5 to -8
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Centre Antoine LACASSAGNE
Nice, 06000, France
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