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Observational Study of Iron Metabolism in Anemia in ICU and Post-Operative Patients

Observational Study of Iron Metabolism in Anemia in ICU and Post-Operative Patients, Role of Hepcidin

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00338234
Acronym
FAIRe
Enrollment
153
Registered
2006-06-20
Start date
2006-06-30
Completion date
2007-12-31
Last updated
2008-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anemia, Cardiac Surgery, Intensive Care

Keywords

anemia, intensive care, cardiac surgery, iron metabolism, hepcidin

Brief summary

Anemia in intensive care and post-operative patients is due to both blood loss (leading to iron loss) and inflammation.

Detailed description

Anemia in intensive care and post-operative patients is due to both blood loss (leading to iron loss) and inflammation. The latter is known to interfere with iron metabolism, inducing iron storage instead of using it for hemoglobin synthesis. The discover of a new regulatory hormone of iron metabolism, hepcidin, may help us to better understand the link between inflammation and iron functional deficit. The aim of our study is to observe the variation of usual iron metabolism biological markers and of hepcidin, in order to define the better marker of iron loss in these clinical situations.

Interventions

None listed

Sponsors

Société Française d'Anesthésie et de Réanimation
CollaboratorOTHER
Institut National de la Santé Et de la Recherche Médicale, France
CollaboratorOTHER_GOV
Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to 88 Years
Healthy volunteers
No

Inclusion criteria

* Anemia (haemoglobin \< 10 g/dL) * Hospitalization in ICU for an expected duration of 7 days or more * Or, day one post cardiac surgery

Exclusion criteria

* Chronic anemia (Hb \< 9 g/dL for more than one month before hospitalization) * Iron metabolism disease

Design outcomes

Primary

MeasureTime frame
Functional iron deficiencyduring the study

Secondary

MeasureTime frame
fatigue assessed by the MFI20 score for cardiac surgery patientsat one day,at seven days and at 28 days

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026