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CompletedNCT01668589

Observational Study of Denosumab (Prolia®) in Postmenopausal Women With Osteoporosis

Prospective Observational Study to Evaluate Medication-taking Behavior With Denosumab (Prolia) and Patient Characteristics in Postmenopausal Women With Osteoporosis in Routine Clinical Practice in Germany, Austria, Greece and Belgium

Status
Completed
Phase
Study type
Observational
Enrollment
1,501 (actual)
Sponsor
Amgen · Industry
Sex
Female
Age
Healthy volunteers
Not accepted

Summary

The main objective of this observational study was to describe medication-taking behavior of patients treated with denosumab for postmenopausal osteoporosis (PMO) at 12 and 24 months.

Detailed description

The decision to treat patients with denosumab was made independent of and before their enrolment in the study. No study drug was administered as part of the study.

Conditions

Timeline

Start date
2011-11-28
Primary completion
2015-08-31
Completion
2015-08-31
First posted
2012-08-20
Last updated
2018-01-30
Results posted
2016-09-20

Locations

144 sites across 4 countries: Austria, Belgium, Germany, Greece

Source: ClinicalTrials.gov record NCT01668589. Inclusion in this directory is not an endorsement.

Observational Study of Denosumab (Prolia®) in Postmenopausal Women With Osteoporosis (NCT01668589) · Clinical Trials Directory