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Clinical Trial Summary

The trial is designed to evaluate prevalence of fragility fracture, their impact on quality of life of SLE patients and disease or treatment variables such as steroids dosage or use of specific drugs like hydroxychloroquine, DMARDs or belimumab. Patients will perform DXA evaluation, blood tests and PROs questionnaires. Moreover, the investigators want to correlate those variables to bone turnover markers and bone metabolism modulators. A secondary aim is also to assess the fracture risk of those patients as described by FRAX and DEFRA tools.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05590390
Study type Observational
Source Azienda Ospedaliera Universitaria Integrata Verona
Contact Giovanni Orsolini, MD, PhD
Phone +390458128035
Email giovanni.orsolini@aovr.veneto.it
Status Recruiting
Phase
Start date December 31, 2022
Completion date December 30, 2023

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