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Prospective clinical study to confirm and extend the correlation between HSD11B1 polymorphisms, bone mineral density, and cortisol metabolism in patients with osteoporosis

Prospective clinical study to confirm and extend the correlation between HSD11B1 polymorphisms, bone mineral density, and cortisol metabolism in patients with osteoporosis - OsteoGene

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00016601
Enrollment
500
Registered
2020-04-30
Start date
2017-12-01
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

M80 M81 M82 E10 E11 E12 E13 E14 E78 F32 F33 F34

Interventions

Group 1: To analyse the individual osteoporosis risk, all examinations recommended by DVO will be performed, including measurements of bone mineral density by Dual-Energy-Xray-absorptiometry (DXA) and

Sponsors

Universitätsmedizin Göttingen
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: > 20% increased 10-year fracture risk

Exclusion criteria

Exclusion criteria: glucocorticoid therapy

Design outcomes

Primary

MeasureTime frame
Association of HSD11B1 SNP genotypes with BMD (bone mineral density) and PDC (post dexamethasone cortisol)

Secondary

MeasureTime frame
Muscle function: Timed-up and go, chair rising, grip strength measurement; Metabolism: LDL cholesterol, HbA1c; Depression: Questionnaire (HADS Score); Bone quality: Trabecular Bone Score (TBS)

Countries

Germany

Contacts

Public ContactHeide Siggelkow

MVZ Endokrinologikum Göttingen

heide.siggelkow@amedes-group.com055163374633

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026