Precision Medicine Approach for Osteoporosis - Follow Up Study
At a glance
Conditions
NCT06264609
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
University of Kentucky
Lexington, Kentuckyno site contact published
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- Paul Netzel, DNP · PRINCIPAL_INVESTIGATOR · University of Kentucky
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
What this trial measures
- Percent change in bone loss12 months
The primary endpoint for the follow up study will be bone loss as determined by the percent change in DXA absolute values of the lumbar spine, femoral neck, total hip and radius measured at baseline, at the end of the one-year trial; and at end of the one year follow up study. DXA is chosen because of its wide availability, low radioactivity exposure, and clinical use.