Dynamics in Bone Turnover Markers During and After Short-term Glucocorticoid Treatment in Patients With an Inflammatory Joint Disease

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age25-90
SponsorDiakonhjemmet Hospital

About this trial

Bone turnover markers (BTMs) are recommended as an important tool in follow-up of osteoporosis treatment. However, there is a lack of knowledge in the reliability of BTMs during and after glucocorticoid treatment. Glucocorticoids suppresses BTMs during treatment with at least 30% and, moreover, glucocorticoids increase the risk of fractures. Patients with an inflammatory joint disease are at increased risk of osteoporosis, and disease flares are often treated with glucocorticoids, which in turn can lead to loss in reliability of the BTMs in patients who also are on osteoporosis treatment.

There is a need of more knowledge on BTM changes during and after glucocorticoid treatment for optimized patientcare, reduced risk of side effects and reduced health economic costs.

Eligibility criteria

Qualifiers

diagnosis of inflammatory rheumatic joint disease

indication of disease modifying treatment initiation with or without glucocorticoids OR

stable DMARD treatment with parenteral glucocorticoid injection

Disqualifiers

known osteoporosis or osteoporosis treatment

women during the transitory phase

oestrogen treatment

any fracture within the last year

Trial design

Treatments tested in this trial

  • Glucocorticoid Effect

Treatment groups

160 Participants
are divided into 6 treatment groups

6

Treatment groups

See each treatment group below.

Sponsors and collaborators

Diakonhjemmet Hospital

Lead sponsor

Vestre Viken Hospital Trust

Collaborator

Hormone Laboratory, Aker University Hospital, Oslo, Norway

Collaborator