Evaluation of Iron Supplementation During Darbepoetin Alfa Treatment in Prophylaxis of Severe Anaemia Chemo-Induced
Neoplasms, Anemia
About this trial
This is an interventional prevention trial for Neoplasms focused on measuring Neoplasms, Solid, Anemia, darbepoetin alfa, ferric saccharose, Venofer®, Aranesp®
Eligibility Criteria
Inclusion Criteria: Age ≥ 18 years Well-informed written consent, signed by the patient Patient picked up for solid tumor treatment, whichever the localization, with or without metastasis Patient revealing, before or during chemotherapy, a moderate anemia, that means: Men: 9<Hb<12 g/dl; Women: 9<Hb<11 g/dl. Patient for who at least four chemotherapy cycles are planed (eight in case of weekly chemotherapy) after inclusion in the study Patients with life expectancy higher than three months Patient with general conditions compatible with the study's follow-up Exclusion Criteria: Contra-indication for Venofer Anemia which can have curative treatment Bloody transfusion during the previous four weeks Documented or suspected medullary invasion Uncontrolled arterial hypertension Acute bacterial infection Transferrin saturation's coefficient Pregnancy Ferric salts oral treatment interrupted since less than one week Patient with bad french language's comprehension Patient with a major psychiatric pathology Patient under guardianship, trusteeship or justice safeguard
Sites / Locations
- Centre Hospitalier de Castres
- Centre Hospitalier de Montauban
- Centre Hospitalier Joseph Ducuing
- Institut Claudius Regaud