RASKAL: Robotic-assisted surgery and kinematic alignment in total knee arthroplasty
- Conditions
- End Stage ArthritisTotal Knee ReplacementOsteoarthritisSurgery - Surgical techniquesMusculoskeletal - OsteoarthritisMusculoskeletal - Other muscular and skeletal disorders
- Registration Number
- ACTRN12621000205831
- Lead Sponsor
- Australian Orthopaedic Association National Joint Replacement Registry
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 300
1.All patients suitable for TKA age 40-80 years with a primary diagnosis of osteoarthritis.
2.Patients who meet the indications for primary unilateral TKA using the Stryker Triathlon cruciate-retaining TKA system.
1.Knee flexion < 90 degrees and knee flexion contracture > 15 degrees at preoperative assessment
2.Coronal deformity with hip-knee-ankle (HKA) angle > 15 degrees varus and > 10 degrees valgus on standing long-leg radiographs
3.Prior grade 3 injury to posterior cruciate ligament, posterolateral corner, lateral collateral ligament or medial collateral ligament
4.TKA requiring increased prosthetic stability (posterior-stabilised, constrained condylar, or rotating hinge designs), diaphyseal stems or metal augments
5.TKA for causes other than osteoarthritis (inflammatory arthritis, post-traumatic arthritis, tumour or acute fracture)
6.Prior contralateral TKA within 6 months of current TKA surgery
7.Any prior knee surgery apart from arthroscopic surgery or anterior cruciate ligament reconstruction
8.Prior femoral, tibial or patellofemoral osteotomies
9.Symptomatic grade 3-4 ipsilateral ankle or hip arthritis
10.The participant unable to attend clinical follow-up for a minimum of 2 years
11.The participant is unable to provide informed consent (due to cognitive capacity or English proficiency)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method