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Efficacy of once weekly teriparatide in patients with glucocorticoid-induced osteoporosis

Not Applicable
Conditions
Glucocorticoid-induced osteoporosis
Registration Number
JPRN-UMIN000011419
Lead Sponsor
Glucocorticoid-induced osteoporosis research group
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
204
Inclusion Criteria

1) Patients who have been taking or are scheduled to take oral steroid at a dose equivalent to 5 mg/day of prednisolone or higher for at least 3 months
2) Patients aged 20 years or older

Exclusion Criteria

1) Patients who previously used bisphosphonate. However, use for up to 2 weeks, 6 months or more before the enrollment is allowed.
2) Patients who have used Teribone or Forteo in the past.
3) Patients for who have contraindications of teriparatide and alendronate.
4) Patients who have 3 or more lumbar vertebral bodies could not be evaluated in DXA.
5) Patients who have used denosumab within the 6 months before enrollment.
6) Patients who were considered as inappropriate for the study by physician.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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