Actively Recruiting
Anterior Cruciate Ligament Reconstruction With a Periosteal - Patellar Tendon - Bone Autograft - The Kocabey Press-Fit Technique
Led by Ankara City Hospital Bilkent · Updated on 2025-01-29
150
Participants Needed
1
Research Sites
104 weeks
Total Duration
On this page
Sponsors
A
Ankara City Hospital Bilkent
Lead Sponsor
K
Konya City Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Anterior Cruciate Ligament Reconstruction With a Periosteal - Patellar Tendon - Bone Autograft - The Kocabey Press-Fit Technique
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients who underwent anatomical single-bundle anterior cruciate ligament reconstruction with periosteal - patellar tendon - bone autograft and press-fit tibial fixation technique after anterior cruciate ligament rupture
- Patients with at least 1 year of clinical and radiological follow-up
- Patients who did not undergo a revision
You will not qualify if you...
- Patients who underwent a secondary arthroscopy for any reason after primary surgery
- Patients with a history of septic arthritis before or after the surgery
- Patients with a history of trauma to the operated knee after primary surgery
- Patients who have not completed at least 1 year of follow-up
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Ankara City Hospital
Ankara, Turkey (Türkiye)
Actively Recruiting
Research Team
E
Enejd Veizi, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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