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UnknownNCT03702140

Examination How the Administration Period of Teriparatide Affects Bone Metabolism and Bone Mineral Density Prior to Denosumab Therapy

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
90 (estimated)
Sponsor
Shinshu University · Academic / Other
Sex
All
Age
20 Years – 120 Years
Healthy volunteers
Not accepted

Summary

The aim of this study is to examine the efficacy and adverse events in the following 3 groups in osteoporosis patients: 1. The administration period of teriparatide is less than 6 months and thereafter, denosumab for 24 months. 2. The administration period of teriparatide is from 6 to 12 months and thereafter, denosumab for 24 months. 3. The administration period of teriparatide is more than 12 months and thereafter, denosumab for 24 months.

Conditions

Interventions

TypeNameDescription
DRUG"Teriparatide", "Forteo® or Teribon"To examine the effects of terimaratide less than 6 months in osteoporosis

Timeline

Start date
2018-10-09
Primary completion
2023-10-08
Completion
2025-10-08
First posted
2018-10-10
Last updated
2021-09-21

Locations

1 site across 1 country: Japan

Source: ClinicalTrials.gov record NCT03702140. Inclusion in this directory is not an endorsement.

Examination How the Administration Period of Teriparatide Affects Bone Metabolism and Bone Mineral Density Prior to Deno (NCT03702140) · Clinical Trials Directory