Partial tears of anterior cruciate ligament: Results of single bundle augmentation.
Dhananjaya Sabat, Vinod Kumar
https://pubmed.ncbi.nlm.nih.gov/26015599/Actively Recruiting
Led by Assiut University · Updated on 2025-12-22
30
Participants Needed
1
Research Sites
N/A
Total Duration
This research aims to clinically evaluate patients with partial anterior cruciate ligament ACL tears who undergo ACL augmentation surgery. The study focuses on assessing knee function primarily using the International Knee Documentation Committee IKDC score to measure outcomes in these patients. The evaluation is conducted at Assiut University Hospital and sponsored by Assiut University. Patients in this study will receive ACL augmentation surgery using a hamstring graft. The graft is fixed to the femoral part with adjustable loop devices, while fixation to the tibial part is done using bio or peak screws, sometimes with additional staples. This procedure is designed for patients with partial ACL tears, including those with or without meniscal tears or knee deformities, and includes both recent and chronic injuries. During the study, participants will undergo clinical evaluations to record IKDC scores at baseline and follow-up to observe changes in knee function after surgery. The main outcome measured is the difference in IKDC scores from baseline. Participants will be monitored throughout the study period, which runs until March 2026, to assess the surgical outcomes and recovery progress.
CONDITIONS
Augmentation of Partial Anterior Cruciate Ligament Tear: Early Results
M
Michael Mikhaeil, Resident
M
Mohamed Abd-El Radi, Lecturer
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Assiut University
Lead Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Day of surgery
Participants undergo ACL augmentation surgery using a hamstring graft fixed with adjustable loop devices and bioscrews +/- staples.
1 visit (in-person)
Duration - Up to 6 months
Participants have clinical evaluations mainly based on IKDC scores after surgery to assess recovery and treatment outcomes.
Approximately 6 post-operative visits
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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Lead Sponsor