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Clinical Trial Summary

The study will explore the performance of the CDMS (Cryo Detector Mass Spectrometer) method in measuring SF (serum ferritin) in human serum of healthy individuals. This will be the first experience of testing SF with this method using biologic material of human origin.


Clinical Trial Description

A clear interpretation of hyperferritinemia is difficult in many clinical situations. Crucial for the correct treatment of patients is the differentiation between reactively elevated ferritin and effective iron overload.The measurement methods that are routinely used provide quantitative results of the measurement of total ferritin molecules independent of their actual iron content.With a modified mass spectrometric method (CDMS), this should be possible. In this study the investigators would like to apply this measurement technique for the first time with human serum as the investigators would like to test healthy blood donors with known normal, low or elevated ferritin levels. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05886309
Study type Observational
Source University Hospital, Basel, Switzerland
Contact
Status Active, not recruiting
Phase
Start date February 12, 2024
Completion date June 2024

See also
  Status Clinical Trial Phase
Not yet recruiting NCT01996683 - Efficacy and Safety of Efficacy and Safety of Continued Iron Chelation Therapy In Poly-transfused Thalassemia Patients With Low Serum Ferritin (< 500 ng/ml) N/A
Recruiting NCT06232642 - Effects of Lactoferrin-enriched Whey on Iron Status in Females N/A