Viewing Study NCT04748510



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Last Modification Date: 2024-10-26 @ 1:56 PM
Study NCT ID: NCT04748510
Status: UNKNOWN
Last Update Posted: 2022-04-29
First Post: 2021-02-04

Brief Title: Functionally Aligned vs Mechanical Axis Aligned Total Knee Arthroplasty
Sponsor: Perth Hip and Knee
Organization: Perth Hip and Knee

Study Overview

Official Title: A Prospective Randomised Control Trial Comparing the Effect of Functional Alignment With Mechanical Axis Alignment on Outcomes After Total Knee Arthroplasty
Status: UNKNOWN
Status Verified Date: 2022-04
Last Known Status: RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: FATKAvsMATKA
Brief Summary: The objective of this study is to compare clinical and radiological outcomes in robotic-arm assisted TKA using mechanical alignment MA TKA versus robotic-arm assisted TKA with functional alignment FA TKA Both FA TKA and MA TKA are performed through similar skin incisions robotic-guidance and use identical implants In MA TKA bone is prepared and implants positioned to ensure that that the overall alignment of the leg is in neutral In FA TKA the bone is prepared and implants positioned to restore the natural alignment of the patients leg Both of these surgical techniques provide excellent outcomes in TKA but it is not known which of the two techniques is better for patient recovery Mako robotic-assisted TKA is an established treatment for arthritis of the knee joint The positions of the implants and overall alignment of the leg are important as they influence how quickly the implants wear out and need replacing The aim of this study is to determine if patient recovery is better with functionally aligned Mako robotic-assisted total knee arthroplasty FA TKA or mechanically aligned Mako robotic-assisted total knee arthroplasty MA TKA
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None