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Study identifier: NCT06733597 Synced from ClinicalTrials.gov · August 04, 2026
● Recruiting

Femoral BMD Change Following Cemented or Cementless Total Knee Arthroplasty

Condition: Knee Arthropathy  ·  Sponsor: University of Wisconsin, Madison

PhaseNA
Planned participants100
Who can joinAll sexes, 55 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of this study is to examine femur bone mineral density (BMD) change before and after surgery in patients receiving cemented or cementless total knee arthroplasty (TKA). performed with manual or robotic methods. 100 participants will be enrolled and can expect to be on study for up to 26 months.

This description comes directly from the study's public registry record.

Talk to the study team

Osteoporosis Clinical Research Program  ·  608-265-6410  ·  uwocrp@aging.wisc.edu

Always discuss trial participation with your own doctor first.

Locations (1)

UW School of Medicine and Public HealthMadison, Wisconsin, United StatesRecruiting

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