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Comparative Effect of Mechanical and Functional Alignment in Bilateral Total Knee Arthroplasty on Ankle Alignment

Comparative Effect of Mechanical and Functional Alignment in Bilateral Total Knee Arthroplasty on Ankle Alignment : a Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06259032
Enrollment
20
Registered
2024-02-14
Start date
2023-10-01
Completion date
2024-06-30
Last updated
2024-11-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Arthropathy of Knee

Brief summary

Mechanical alignment (MA) in total knee arthroplasty (TKA) is the most commonly used with well-documented long-term results, however 20% of patients express dissatisfaction following primary TKA. Alternative alignment philosophies have been proposed, aiming to improve patient clinical outcomes and satisfaction. However, evaluation is focused mainly on knee alignment, the pathological findings and other adaptational changes in the ankles and hips are usually neglected. Thia study aim to comparative effect between mechanical and functional alignment in patient undergone bilateral robotic TKA on ankle alignment and functional outcomes.

Interventions

Goal alignment in TKA with mechanical alignment, resection bone in perpendicular to mechanical axis of femur and tibia.

OTHERFunctional alignment

Goal alignment in TKA with functional alignment, resection of bone base on native joint line obliquity.

Sponsors

Department of Medical Services Ministry of Public Health of Thailand
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Age 20-80 years * Symptomatic bilateral knee Osteoarthritis requiring primary TKA * Willing to undergo bilateral simultaneous TKA * Able to give informed consent

Exclusion criteria

* ligament deficiency requiring constrained prosthesis * bone loss with augmentation need * history of fracture around knee or previous osteotomy * history of ankle fracture * patient with neuromuscular disorder or movement disorder * patient is unable to attend the study follow-up program

Design outcomes

Primary

MeasureTime frameDescription
Radiographic outcomes : Hip-knee-ankle anglepre-operative within 2 weeks and post-operative at 2,4,8,12 weeksangle in degree between line from center of head of Femur to intercondylar notch and line from tibial interspinous to center of tibial plafond
Radiographic outcomes : Tibiotalar tilt anglepre-operative within 2 weeks and post-operative at 2,4,8,12 weeksangle in degree between subchondral plate of distal tibial articular surface and talar dome
Radiographic outcomes :Talar inclinationpre-operative within 2 weeks and post-operative at 2,4,8,12 weeksangle in degree between talar dome and vertical axis
Radiographic outcomes : Tibial plafond inclinationpre-operative within 2 weeks and post-operative at 2,4,8,12 weeksangle in degree between subchondral plate of distal tibial articular surface and vertical axis

Secondary

MeasureTime frameDescription
Clinical outcomes : American Orthopaedic Foot and Ankle Society (AOFAS) Ankle-Hindfoot Scorepre-operative within 2 weeks and post-operative at 2,4,8,12 weeksevaluation of the clinical status of the ankle-hindfoot, both subjective and objective information. Patients report their pain, and physicians assess alignment. The patient and physician work together to complete the functional portion. Scores range from 0 to 100, with healthy ankles receiving 100 points.
Clinical outcomes : Knee injury and Osteoarthritis Outcome Score (KOOS)pre-operative within 2 weeks and post-operative at 2,4,8,12 weeksa questionnaire assesses patient pain (9 items), other symptoms (7 items), function in daily living (17 items), function in sport and recreation (5 items), and knee related quality of life (4 items). Scores range from 0 to 100 with a score of 0 indicating the worst possible knee symptoms and 100 indicating no knee symptoms.
Quality of Life score : EQ-5D-5Lpre-operative within 2 weeks and post-operative at 2,4,8,12 weeksassess patient five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels, Index scores range from -0.42 to 1; 1 is the best possible health state. Negative values represent health states perceived as worse than dead, which is equal to 0.
Forgotten Joint Scorepre-operative within 2 weeks and post-operative at 2,4,8,12 weeksconsists of 12 questions and is transform on a 0-100 scale.The higher the score, the less the patient is aware of their affected joint when performing daily activities

Other

MeasureTime frameDescription
Other outcomes : blood losspost operative with in 2 daysrecord in millilitre measured from Radivac drain
Other outcomes : operative timeintraoperativemeasured in minutes from skin incision to complete of skin suture
Other outcomes : Range of knee motionpost-operative at 2,4,8,12 weeksrecord in total degree of knee motion
complicationspost-operative at 2,4,8,12 weeksYes (complications) or No ( no complications) if yes, will specified the complications complication such as bone fracture, wound dehiscence, surgical site infection, periprosthetic infection ,pulmonary embolism or other adverse outcomes that may or may not directly associated with the operation.
Other outcomes : pain score (Visual analog scale)post-operative at 2,4,8,12 weeksscore from 0-10 (0 was no pain, 10 was worst pain )
Other outcomes : soft tissue releaseintraoperativeintra-operative soft tissue release (medial collateral ligament release or others structure around knee) report with Yes (soft tissue release) or No (no soft tissue release)

Countries

Thailand

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026