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Clinical Trials in Italy / NCT06637137
Recruiting Observational

Patient Blood Management in Patients Scheduled for Cardiac Surgery

NCT06637137 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2025-02-24
Last updated
2026-09-10

Condition(s) studied

AnemiaAnemia, Iron-DeficiencyIron Deficiency Anemia TreatmentIron Deficiency Anemia (IDA)Cardiac Surgical PatientsBlood Loss, Surgical

Investigational drug(s) / intervention(s)

Iron →

Iron: Patients who present a state of hypoferritinemia or a state of reduced transferrin saturation will undergo administration of i.v iron at least 2 weeks before scheduled cardiac surgery, plus acid folic and B vitamin co-administration.

Study summary

The ICARUS 2 study has the general objective of collecting data in patients undergoing cardiac surgery; in our centre, in order to optimize and improve hemoglobin values, a team of haematologists, assisted by cardio anesthetists and cardiac surgeons, will evaluate the blood tests of patients scheduled for elective cardiac surgery in order to correct any states of hypoferritinemia (low iron in the blood) to promote recovery from blood losses related to cardiac surgery. This objective is strongly encouraged by the good use of blood programs currently in force at our foundation.

In particular, the research presented here intends to demonstrate a reduction in the number of intra- and post-operative transfusions.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: \- all adult patients scheduled for elective cardiac surgery Exclusion Criteria: * pregnancy * dyalisis * patient's refusal

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Fondazione Policlinico Gemelli IRCCS Roma Italy Recruiting

More Fondazione Policlinico Universitario Agostino Gemelli IRCCS trials in Italy

Other trials for the same condition

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 NCT06637137 on ClinicalTrials.gov ↗ ← All trials in Italy