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UnknownNCT02166437

Clinical Results of Bisphosphonate and Denosumab Therapy Following Teriparatide Therapy for Japanese

Clinical Results of Bisphosphonate and Denosumab Therapy Following Teriparatide Therapy for Japanese, Prospective Study

Status
Unknown
Phase
Study type
Observational
Enrollment
500 (estimated)
Sponsor
Tomidahama Hospital · Academic / Other
Sex
All
Age
45 Years
Healthy volunteers
Not accepted

Summary

In this study, the investigators would like to analyze the bone mineral density (BMD) , bone turnover makers, and fracture prevention effects of bisphosphonate and denosumab randomly divided following daily teriparatide in Japanese patients under clinical practice. The participants are treated in the investigators hospital, who are under severe osteoporotic condition.

Detailed description

Registry criteria: Patients treated in the investigators hospital using teriparatide. Enrolled patients are severe osteoporosis; more than two previous osteoporotic fractures, low BMD (\< young adult mean 65%). Interventions: blood analyses and dual-energy X-ray absorptiometry (DXA) every 4 months Informed consent: Written informed consent will be obtained. Sample size: Five-hundreds participants

Conditions

Timeline

Start date
2013-11-01
Primary completion
2017-11-01
Completion
2018-11-01
First posted
2014-06-18
Last updated
2016-10-19

Locations

1 site across 1 country: Japan

Source: ClinicalTrials.gov record NCT02166437. Inclusion in this directory is not an endorsement.

Clinical Results of Bisphosphonate and Denosumab Therapy Following Teriparatide Therapy for Japanese (NCT02166437) · Clinical Trials Directory