Viewing Study NCT06135454



Ignite Creation Date: 2024-05-06 @ 7:47 PM
Last Modification Date: 2024-10-26 @ 3:13 PM
Study NCT ID: NCT06135454
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-02-15
First Post: 2023-11-13

Brief Title: Comparison of Outcomes Between Open Wedge High Tibial Osteotomy and Double Level Osteotomy in Antromedial Knee Arthritis With Extra Articular Deformity
Sponsor: Assiut University
Organization: Assiut University

Study Overview

Official Title: Open Wedge High Tibial Osteotomy Versus Double Level Osteotomy
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-02
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 compare the radiographic and clinical outcomes of varus osteoarthritic knees treated with an open-wedge high tibial osteotomy OWHTO alone or with a double-level osteotomy DLO It was hypothesized that treatment with DLO would prevent the joint line obliquity JLO optimize post-operative limb alignment and provide better clinical and radiological outcomes after surgery than medial opening-wedge high tibial osteotomy OWHTO alone for patients with medial compartment osteoarthritis
Detailed Description: Osteoarthritis is a degenerative joint disease characterized by erosion of the articular cartilage hypertrophy of the bone at the margins and subchondral sclerosis1 Osteoarthritis of the knee is a common problem causing significant knee pain and disability Medial compartment osteoarthritis is predisposed to be varus deformity of the knee2 High tibial osteotomy HTO is a well-established method for treatment of medial Uni compartmental-knee osteoarthritis and correction of varus deformity3Double level osteotomy recently used as another method for treatment this problem to improve outcomes and decrease complication4

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