Femoral Bone Mineral Density (BMD) Change Following Cemented or Cementless Total Knee Arthroplasty

Status: Recruiting
Location: See location...
Intervention Type: Other, Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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 14 months.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 55
Healthy Volunteers: f
View:

• 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, i.e., 10-year major osteoporotic fracture risk greater then or equal to 20 percent or hip fracture risk greater than or equal to 3 percent.

Locations
United States
Wisconsin
UW School of Medicine and Public Health
RECRUITING
Madison
Contact Information
Primary
Osteoporosis Clinical Research Program
uwocrp@aging.wisc.edu
608-265-6410
Time Frame
Start Date: 2025-03-06
Estimated Completion Date: 2026-12
Participants
Target number of participants: 100
Treatments
Active_comparator: Cemented and Manual
Active_comparator: Cemented and Robotic
Active_comparator: Cementless and Manual
Active_comparator: Cementless and Robotic
Related Therapeutic Areas
Sponsors
Leads: University of Wisconsin, Madison

This content was sourced from clinicaltrials.gov