Does the use of the Verasense pressure sensor device and alignment method produce a more balanced knee in patients undergoing total knee arthroplasty

Not Applicable

Completed

• Conditions: Osteoarthritis; Musculoskeletal - Osteoarthritis; Surgery - Surgical techniques

• Registration Number: ACTRN12616001705471
• Lead Sponsor: The Orthopaedic Research Institute of Queensland (ORIQL)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-12-13
• Study Completion: 2020-03-03
• Last Update Posted: 22 February 2021

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 124

Inclusion Criteria

Male or Female
Age 45-80 years of age
BMI<40
Patients who require primary TKA for treatment of osteoarthritis

Exclusion Criteria

Previous open knee surgery
Previous high tibial osteotomy
Previous ligamentous injury to the collateral ligaments
Previous fracture of the tibia or femur
Varus or valgus deformity >15 degrees
Fixed tibial subluxation due to posterior bone wear
Hyperextension deformity

Study & Design

• Study Type: Interventional
• Study Design: Not specified