Clinical Trials Directory

Trials / Completed

CompletedNCT00338234

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
Phase
Study type
Observational
Enrollment
153 (actual)
Sponsor
Assistance Publique - Hôpitaux de Paris · Academic / Other
Sex
All
Age
20 Years – 88 Years
Healthy volunteers
Not accepted

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.

Conditions

Timeline

Start date
2006-06-01
Primary completion
2007-12-01
Completion
2007-12-01
First posted
2006-06-20
Last updated
2008-05-06

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT00338234. Inclusion in this directory is not an endorsement.