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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04307251
Other study ID # COA 012/2563
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 23, 2020
Est. completion date February 25, 2021

Study information

Verified date March 2020
Source Navamindradhiraj University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to compare post-operative mechanical alignment (Hip-Knee-Ankle angle; HKA) between imageless robotic-assisted (Navio™ Robotics-assisted Surgical System) and Conventional Total Knee Arthroplasty


Recruitment information / eligibility

Status Completed
Enrollment 168
Est. completion date February 25, 2021
Est. primary completion date January 30, 2021
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Primary osteoarthritis of knee who were scheduled for a primary total knee arthroplasty - Age 50-80 year - Patients with osteoarthritis who voluntarily participated in the project Exclusion Criteria: - Patients with osteoporosis - History of inflammatory arthroplathy - Previous fracture or open surgery on the same knee - Patients with bilateral total knee arthroplasty - Patients osteoarthritis with revision surgery

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Navio™ Robotics-assisted Surgical System, LEGION Total Knee System
Robotic TKA uses computer software to convert anatomical information into a virtual patient-specific 3D reconstruction of the knee joint.The surgeon uses this virtual model to plan optimal bone resection, implant positioning, bone coverage, and limb alignment based on the patient's unique anatomy.
Conventional, LEGION Total Knee System
Total Knee Arthroplasty (TKA) is a widespread orthopaedic procedure for restoring functionality and minimizing pain due to end stage osteoarthritis. Conventional TKA, well-accepted as the standard of care, is performed with manual instrumentation guided by intramedullary or extramedullary alignment rods, as well as rotational guides that are not patient-specific.

Locations

Country Name City State
Thailand Navamindradhiraj University Dusit Bangkok

Sponsors (1)

Lead Sponsor Collaborator
Navamindradhiraj University

Country where clinical trial is conducted

Thailand, 

Outcome

Type Measure Description Time frame Safety issue
Primary Mechanical axis Post-operative Mechanical Alignment; Hip-Knee-Ankle angle; If you divide the knee into quadrants, the ideal mechanical axis would bisect the knee (0), with medial zone (-1) or lateral zone (-1) being within physiologic range. With the notable exception of physiologic varus Change from baseline mechanical axis at 6 weeks after surgery
Secondary Knee Society and Knee Society function score Knee Society and Knee Society function score (minimum 0, maximum 200) Change from baseline Knee Society and Knee Society function score at 3 months, 6 months, and 12 months after surgery
Secondary Range of motion of knee Range of motion of knee (minimum 0, maximum 140) Change from baseline Range of motion of knee at 3 months, 6 months, and 12 months after surgery
Secondary Oxford knee score Oxford knee score (minimum 0, maximum 48) Change from baseline Oxford knee score 3 months, 6 months, and 12 months after surgery
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