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Clinical Trial Summary

In total 50 subjects with iron deficiency anemia treated with intravenous iron are planned for inclusion in this trial. After signing an informed consent a blood sample will be obtained from each participant before iron treatment. The investigators will measure the thrombin generation in plasma assessed by the calibrated automated thrombogram (CAT). patient will go face to face interview and will be asked to answer structured questionnaire which will include information on demographics, clinical data ( fever, allergies , etc.) and comorbidities

Two weeks after completing intravenous iron administration additional blood samples will be taken: thrombin generation will be measured


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02129907
Study type Observational [Patient Registry]
Source HaEmek Medical Center, Israel
Contact
Status Completed
Phase
Start date October 2013
Completion date December 2015