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2023-506949-27-00CompletedPhase 2

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

Identifying Individuals at Risk of Glucocorticoid-Induced Impairment of Bone Disease (RIGID)

Source: EU CTIS (euclinicaltrials.eu) · Last updated 5 Dec 2025

Next steps

Brief summary (registry, in English)

The main objective of the study is to detect a biomarker(s) that identifies individuals at risk of Glucocorticoid-Induced Impairment of Bone Disease

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
36 (actual)
First submitted
22 Jan 2024
Start date
14 Oct 2024
Lead sponsor
Odense University Hospital
Diseases
Osteoporosis
EU CT number
2023-506949-27-00

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 36
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Vaccination with living or weaken viral or bacterial vaccines in patient who or immunocompromised. In these cases, prednisolone treatment should not be administered two weeks before and after vaccination.
  • Previous gastric bypass and/or known ongoing malabsorption

Other illness

  • Allergy to prednisolone or one of the excipients
  • Systematic fungal infections
  • Not able to provide informed consent (e.g., dementia, not able to understand Danish). At the information meeting the investigator will make an individual assessment to evaluate whether a potential study participants understand the information.
  • Known Cushing’s syndrome
  • Severe covid-19 in the last 3 month (defined as needing dexamethasone treatment)
  • Menopause (defined as 1 year without menstrual bleeding)
  • Ongoing infection

Lab values

  • Chronic kidney disease (eGFR <30)

Other

  • Uncontrolled thyrotoxicosis
  • Use of oral or inhaled GCs within the past year
  • Pregnancy (defined as elevated HCG)

Who the study is looking for

  • Men and women aged 18-50 years

Age in the registry: 18 years to 64 years · Sex: All · Accepts healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (2)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Esbjerg Og Grindsted SygehusEsbjergDenmarkCompleted
Odense University HospitalOdense CDenmarkCompleted

Are you the coordinator? Confirm the details

This page is information, not medical advice. Discuss any trial with your doctor.