Ignite Creation Date:
2025-12-24 @ 7:18 PM
Ignite Modification Date:
2025-12-25 @ 4:57 PM
Study NCT ID:
NCT04958603
Status:
COMPLETED
Last Update Posted:
2021-07-12
First Post:
2021-06-27
Is NOT Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
The Clinical Effect of Different Lateral Retinaculum Relaxation Methods in the Treatment of LPCS
Sponsor:
Peking University Third Hospital
Organization:
Study Overview
Official Title:
The Clinical Effect of Different Lateral Retinaculum Relaxation Methods in the Treatment of Lateral Patellar Compression Syndrome
Status:
COMPLETED
Status Verified Date:
2021-06
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:
To observe the comparison of the clinical effects of two different ways of loosening the lateral support band under arthroscopy to treat lateral patella excessive compression syndrome.
Detailed Description:
To analyze the surgical conditions of 64 patients with lateral patella excessive compression syndrome who were surgically treated by Deputy Chief Physician Yang Yuping of the Department of Sports Medicine, Peking University Third Hospital from September 2004 to January 2019. Among them, 24 early cases used the traditional proximal release of the lateral retinaculum (traditional surgical group), and recently 40 cases, after learning from the surgical experience of the early cases, switched to the lateral release of the lateral retinaculum, that is, "L" type Release (new surgery group). The visual analog scale (VAS), Lysholm score, and IKDC knee function subjective evaluation scale (IKDC) score were performed before and after the operation. By analyzing the knee movement scores of patients before and after surgery, the efficacy of the above two operations was judged, and the two groups of postoperative scores were evaluated.
Study Oversight
Has Oversight DMC:
False
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?: