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Clinical Trial Summary

Previous studies have shown that there is a large inter-individual variability in the degree of bone loss during glucocorticoid treatment, and while some patients experience extensive bone loss other patients' bone mass remains stable. The aim of the study is to find a biomarker that can be used to identify individuals at risk of glucocorticoid-induced bone loss. The study will include 36 healthy volunteers, that will be randomized to receive either glucocorticoid treatment or placebo. During the study blood samples, bone marrow samples, bone tissue samples, and adipose tissue samples are taken and a mixed meal test is performed.


Clinical Trial Description

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Study Design


Related Conditions & MeSH terms


NCT number NCT06421597
Study type Interventional
Source Odense University Hospital
Contact Catharina Vind Nielsen, MD
Phone +45 21351124
Email catharina.vind.nielsen@rsyd.dk
Status Not yet recruiting
Phase Phase 2
Start date May 2024
Completion date December 2025