Ignite Creation Date:
2024-05-06 @ 6:45 PM
Last Modification Date:
2024-10-26 @ 2:54 PM
Study NCT ID:
NCT05778539
Status:
COMPLETED
Last Update Posted:
2023-03-21
First Post:
2023-02-27
Brief Title:
Lateral Retinacular Release in Total Knee Arthroplasty With Patellar Replacement
Sponsor:
Hospital del Mar
Organization:
Hospital del Mar
Study Overview
Official Title:
Systematic Lateral Retinacular Release Does Not Reduce Post-Operative Anterior Knee Pain After Primary Total Knee Arthroplasty With Patellar Replacement
Status:
COMPLETED
Status Verified Date:
2023-03
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:
The aim of this study is to assess the effect of systematic lateral retinacular release on anterior knee pain as well as its impact on the functional and radiological outcomes after total knee arthroplasty with patellar resurfacing
Detailed Description:
Anterior knee pain is an important cause of persistent pain after total knee arthroplasty Lateral retinacular release has been proposed as a procedure to prevent anterior knee pain syndrome based on the reduction of lateral tension and improving patellar tracking
However its effect on anterior knee pain after total knee arthroplasty is not clear when it is not strictly needed to correct maltracking
The purpose of this trial is to evaluate the effect of systematic lateral retinaculare release on anterior knee pain peformed during a total knee arthroplasty with patellar resurfacing
However its effect on anterior knee pain after total knee arthroplasty is not clear when it is not strictly needed to correct maltracking
The purpose of this trial is to evaluate the effect of systematic lateral retinaculare release on anterior knee pain peformed during a total knee arthroplasty with patellar resurfacing
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