drugset / Trial / NCT06421597

Identifying Individuals at Risk of Glucocorticoid-Induced Impairment of Bone Disease

NCT06421597

RandomizedParallel-groupQuadruple-blindTreatment

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 an oral glucose tolerance test is performed.

Timeline

Start
2024-11-04
Primary completion
2026-03-30
Completion
2026-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Prednisolone Other / unclassified 25 mg

Indications