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Trials / Recruiting

RecruitingNCT06309433

Assessment of Periprosthetic Bone Mineral Density in Patients Undergoing Total Knee Prosthesis of Different Design

Assessment of Bone Mineral Density at the Interface With the Femoral and Tibial Components in Patients Undergoing Total Knee Prosthesis of Different Design and Material

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
Istituto Ortopedico Rizzoli · Academic / Other
Sex
All
Age
45 Years
Healthy volunteers
Not accepted

Summary

compare changes in BMD via DXA at the level of the femoral and tibial periprosthetic bone between two groups of patients undergoing cemented TKA of different design (posterior stabilization vs posterior cruciate preservation) with proms at a 2-year follow-up.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTdual energy x-ray absorptiometryPatient will undergo periodic (6-12-24m) dexa scans on the periprosthetic bone

Timeline

Start date
2023-08-30
Primary completion
2027-12-01
Completion
2028-04-01
First posted
2024-03-13
Last updated
2026-03-27

Locations

2 sites across 1 country: Italy

Source: ClinicalTrials.gov record NCT06309433. Inclusion in this directory is not an endorsement.