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A comparative study of the efficacy and safety of romosozumab and teriparatide for glucocorticoid-induced osteoporosis 1

A comparative study of the efficacy and safety of romosozumab and teriparatide for glucocorticoid-induced osteoporosis 1 - A comparative study of the efficacy and safety of romosozumab and teriparatide for glucocorticoid-induced osteoporosis 1

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000056386
Enrollment
100
Registered
2025-02-01
Start date
2025-08-26
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

glucocorticoid-induced osteoporosis

Interventions

Sponsors

Division of Rheumatology, Department of Internal Medicine, Toho University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients 40 years of age or older newly initiating glucocorticoids, meeting the criteria for initiation of pharmacological therapy for glucocorticoid-induced osteoporosis 2) Patients who have provided written informed consent.

Exclusion criteria

Exclusion criteria: 1) Patients with contraindications to romosozumab or denosumab. 2) Patients with active infection or malignancy. 3) Patients who are currently pregnant, lactating, or willing to get pregnant. 4) Patients who do not give consent to this study. 5) Patients previously treated with romosozumab or teriparatide

Design outcomes

Primary

MeasureTime frame
The percent change of bone mineral density of the lumbar spine (L2-4), femoral neck and total hip at 52 and 104 weeks in the romosozumab and teriparatide groups.

Countries

Japan

Contacts

Public ContactMai Kawazoe

Toho University School of Medicine Division of Rheumatology, Department of Internal Medicine

mai.kawazoe@med.toho-u.ac.jp03-3462-4151

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026