Femoral BMD Change Following Cemented or Cementless Total Knee Arthroplasty

Recruiting N/A Interventional Study
Knee Arthropathy
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
55 and older
Sex
Any
Study type
Interventional
Purpose
Basic Science
Participants needed
100 (estimated)
Sponsor
University of Wisconsin, Madison · Other
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About This Trial

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.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patients age greater than or equal to 55 years undergoing TKA with no prior total joint arthroplasty on the surgical side * Normal BMD or osteopenia with Fracture Risk Assessment Tool (FRAX) not meeting Bone Health and Osteoporosis Foundation (BHOF) treatment recommendations, …
Contacts

Osteoporosis Clinical Research Program

608-265-6410

uwocrp@aging.wisc.edu

CONTACT