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Recruiting Observational

Application of Patient Blood Management in the Oncology Patient Affected by Breast Cancer

NCT06883201 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2023-01-31
Last updated
2025-03-19

Condition(s) studied

Breast Cancer

Study summary

Evaluation of the percentage of transfusions in patients with breast cancer undergoing surgery after preventive treatment with haematinics.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * age \> 18 years; * patients diagnosed with histologically confirmed breast cancer and whether or not they have undergone neoadjuvant chemotherapy; * patients who are candidates for destructive and reconstructive breast surgery or not; * Hb values less than or equal to 11 g/dL and/or transferrin saturation less than or equal to 20%; * written informed consent. Exclusion Criteria: * patients with known allergies to ferric carboxymaltose or its excipients; * ferritin values greater than 500 ng/ml; * patients unable to sign consent and comply with procedures.

Primary outcome measure(s)

  • Number of transfusions — 18 months
    To evaluate the percentage, in number of transfusions in patients affected by breast cancer, candidates for destructive and/or reconstructive breast surgery after preventive treatment with haematinics

Trial sites (1)

FacilityCityRegionStatus
"Regina Elena" National Cancer Institute Rome Italy Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06883201 on ClinicalTrials.gov ↗ ← All trials in Italy