Viewing Study NCT06297746



Ignite Creation Date: 2024-05-06 @ 8:13 PM
Last Modification Date: 2024-10-26 @ 3:23 PM
Study NCT ID: NCT06297746
Status: COMPLETED
Last Update Posted: 2024-03-08
First Post: 2024-03-01

Brief Title: Subvastus vs Medial Parapatellar Approaches in Total Knee Arthroplasty With Quadriceps Muscle Elastography
Sponsor: Istanbul University - Cerrahpasa IUC
Organization: Istanbul University - Cerrahpasa IUC

Study Overview

Official Title: Comparison of Early Outcomes of Primary Total Knee Arthroplasties Performed Using Subvastus and Medial Parapatellar Approaches and Evaluation of Quadriceps Muscle Elastography
Status: COMPLETED
Status Verified Date: 2024-03
Last Known Status: None
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: None
Brief Summary: ABSTRACT

INTRODUCTION

Knee osteoarthritis is a common joint pathology causing joint pain and ambulatory limitations In primary total knee arthroplasty TKA surgeries medial parapatellar MP and subvastus SV approaches are frequently used The MP approach provides good exposure and is more widely used In the SV approach the vastus medialis muscle is preserved Some argue that the extensor mechanism may heal earlier with the SV approach In this study unlike previous studies the investigators aimed to quantitatively compare the early outcomes of MP and SV approaches through shear wave elastography SWE measurements isolated over the vastus medialis and vastus lateralis muscles

MATERIALS AND METHODS

The study included 20 patients with indications for TKA due to primary osteoarthritis divided into MP and SV groups SWE measurements of the vastus medialis and vastus lateralis muscles were performed preoperatively and at 3-month follow-up Clinical scores Knee Society Score and WOMAC and straight leg raising time were recorded both preoperatively and postoperatively
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