Arthroscopic reconstruction of the anterior cruciate ligament. A comparison of patellar tendon autograft and four-strand hamstring tendon autograft.
I S Corry, J M Webb, A J Clingeleffer...
https://pubmed.ncbi.nlm.nih.gov/10424213Actively Recruiting
Led by Khyber Medical University Peshawar · Updated on 2026-01-16
64
Participants Needed
1
Research Sites
7 weeks
Total Duration
K
Khyber Medical University Peshawar
Lead Sponsor
K
Khyber Medical College, Peshawar
Collaborating Sponsor
Researchers are evaluating two types of tendon grafts for anterior cruciate ligament (ACL) reconstruction in patients aged 18 years and older with isolated ACL injuries. This prospective, single-blinded, randomized controlled trial aims to compare early functional outcomes using the Lysholm Knee Score at 6 weeks and 3 months after surgery. The goal is to determine if the peroneus longus tendon (PLT) graft is not inferior to the commonly used hamstring tendon (HST) graft. The study is conducted at a single center with ethical approval and informed consent from participants. Participants will be randomly assigned to receive ACL reconstruction using either the hamstring tendon autograft or the peroneus longus tendon autograft. Both procedures involve arthroscopic surgery under spinal anesthesia, with graft fixation using an Endobutton on the femoral side and an adjustable button system on the tibial side following a standard single-bundle technique. The PLT graft is harvested through a small incision near the ankle with a tenodesis of the peroneus brevis performed at the donor site. All patients will follow a standardized rehabilitation protocol after surgery. Throughout the study, participants will undergo assessments of knee instability and knee function at 6 weeks and 3 months post-surgery using validated scoring tools. The outcome assessor will be blinded to the treatment groups to ensure unbiased evaluation. The research team will monitor functional recovery and record any complications. The total study duration includes the surgical intervention and follow-up visits to collect data on early functional outcomes.
CONDITIONS
Comparative Study of Functional Outcomes Between Peroneus Longus and Hamstring Tendon Autografts in Arthroscopic ACL Reconstruction
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Day of surgery and immediate recovery period
Participants undergo arthroscopic anterior cruciate ligament (ACL) reconstruction using either a hamstring tendon or peroneus longus tendon autograft, followed by standard surgical recovery.
1 surgery visit (in-person)
Duration - 3 months after surgery
Participants are assessed for knee instability and function at scheduled follow-up visits after surgery.
2 visits (at 6 weeks and 3 months, in-person)
Total: 1 location
1
Khyber Teaching Hospital
Peshawar, KPK, Pakistan, 25100
Actively Recruiting
D
Dr Syed Dil Bagh Ali Shah, MBBS
D
Dr Syed Muhammad Shabbir Ali Naqvi, MSPT
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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