Ignite Creation Date:
2024-05-06 @ 7:57 PM
Last Modification Date:
2024-10-26 @ 3:17 PM
Study NCT ID:
NCT06190223
Status:
RECRUITING
Last Update Posted:
2024-01-05
First Post:
2023-11-28
Brief Title:
Anterior Cruciate Ligament Reconstruction With a Periosteal - Patellar Tendon - Bone Autograft - The Kocabey Press-Fit Technique
Sponsor:
Ankara City Hospital Bilkent
Organization:
Ankara City Hospital Bilkent
Study Overview
Official Title:
Anatomic Single Bundle Anterior Cruciate Ligament Reconstruction With a Press-fit Tibial Fixation Technique Using Periosteal - Patellar Tendon - Bone Autograft
Status:
RECRUITING
Status Verified Date:
2024-01
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:
This study aims to evaluate the clinical and radiological outcomes of patients undergoing anatomical single-bundle anterior cruciate ligament reconstruction with periosteal-patellar tendon-bone autograft and press-fit tibial fixation technique The study also aims to compare these outcomes with other reconstruction techniques in the literature The research investigates the results of a novel surgical technique providing a minimally invasive and faster rehabilitation for patients undergoing surgery due to anterior cruciate ligament rupture The technique does not use any screws or staples for tibial fixation but it carries similar risks as existing techniques The technique similar to the well-known bone-patellar tendon-bone BPTB autograft technique creates minimal bone defect at the tibial tuberosity Over time the defect remodels and causes minimal clinical discomfort Despite these limitations the authors expect patients operated with the investigated new technique to experience less postoperative swelling less pain faster mobilization and earlier rehabilitation
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