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Clinical Trials in Germany / NCT02719314
Recruiting Observational

Glucocorticoid-induced Osteoporosis in Patients With Chronic Inflammatory Rheumatic Diseases or Psoriasis

NCT02719314 · tracked via the Priya Life Science Germany tracker
Sponsor
Prof Dr Frank Buttgereit
Phase
Observational
Started
2015-12
Last updated
2025-02-13

Condition(s) studied

OsteoporosisInflammatory Rheumatism

Investigational drug(s) / intervention(s)

Glucocorticoid treatment →

Glucocorticoid treatment: Glucocorticoid treatment

Study summary

Glucocorticoids remain to be among the most important and most frequently used anti-inflammatory and immunosuppressive or immune-modulatory acting drugs to treat rheumatic (and other) diseases. Unfortunately, glucocorticoids also exert undesired effects, especially if higher dosages have to be given over longer periods of time. The available data describing frequency and severity of these adverse effects are fragmentary. This statement is especially true for glucocorticoid-induced osteoporosis (GIOP) in the context of chronic inflammatory rheumatic diseases or (in part) psoriasis(arthritis). The state of knowledge and scientific data, being sparse, is partly conflicting and often derived from over-aged projects or studies. Therefore, there are urgent needs to work on various current questions systematically and at the highest scientific level possible. In order to address these needs, we aim at collecting and analyzing disease- and bone-related data from patients with chronic inflammatory rheumatic diseases or psoriasis and therapy with glucocorticoids, and to build a respective GIOP-Databank. Patients will attend for diagnostics, and where necessary therapy and follow-up of GIOP, according to current guidelines. Clinical, laboratory and instrumental examination results from more than 1000 patients in the first three years of the project are planned to be documented in a prospective database.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: Every patient has to fulfill the following inclusion criteria: * patients with (control group: without) a diagnosis of a chronic inflammatory rheumatic disease or psoriasis * patients who (not for control groups) have/had already a glucocorticoid therapy, or patients in which the implementation of a new long-term GC therapy is expected * patients who, according to the Dachverband Osteologie (DVO, Germany) guidelines, attend our osteoporosis and bone metabolism outpatient consultation hours or are referred by the hospital wards of the Charité for diagnosis, treatment or follow-up * capability to understand the patient information * consent to participation in the project and storage of data Exclusion Criteria: If any of the following exclusion criteria is true, the patient must not be included in this study: * alcohol, medication and/or drug addiction * severe psychiatric diseases limiting the comprehension of the project plan and the study protocol (persons incapable of giving informed consent) * pregnant and lactating patients * patients incapable of giving informed consent for any reason * prisoners and all persons who are committed to an institution due to an official or judicial order

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Charité University Medicine Berlin (CCM) Berlin Germany Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT02719314 on ClinicalTrials.gov ↗ ← All trials in Germany