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NCT07762989
Donor Ankle Sensorimotor Recovery After ACL Reconstruction With a Peroneus Longus Tendon Autograft
Conditions: Anterior Cruciate Ligament Injury, Anterior Cruciate Ligament Reconstruction, Donor Site Complication
Sex: All
Ages: 18 Years – 55 Years
Healthy volunteers: No
Enrollment: 20
Sponsor: Gazi University
Location: Gazi University Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation, Sports Health Unit Çankaya Ankara
Summary
This prospective longitudinal observational cohort study will characterize recovery of donor-ankle sensorimotor function in adults who have undergone primary anterior cruciate ligament reconstruction using a peroneus longus tendon autograft. Twenty participants aged 18 to 55 years will be evaluated at postoperative 6-8 weeks, 3 months, and 6 months. The donor limb and the contralateral non-donor limb will be compared using surface electromyography of the peroneus longus, force-platform measures of postural control, inertial-sensor gait analysis, active ankle joint-position sense testing, and clinical and patient-reported foot and ankle function measures. The study does not assign the surgical procedure or rehabilitation treatment.
Eligibility Criteria
Inclusion Criteria:
* Age 18 to 55 years.
* Unilateral primary anterior cruciate ligament tear confirmed by clinical examination and magnetic resonance imaging.
* Primary anterior cruciate ligament reconstruction performed using a peroneus longus tendon autograft.
* Able and willing to attend the postoperative assessments at 6-8 weeks, 3 months, and 6 months.
* Written informed consent provided before study participation.
Exclusion Criteria:
* Multiligament knee injury.
* Previous surgery on the index knee or donor ankle.
* Pre-existing ankle instability or major foot or ankle pathology.
* Neurological or neuromuscular disease.
* Inflammatory or systemic disease that may affect the assessments.
* Major lower-extremity deformity that may affect the assessments.
* Unable to complete the postoperative rehabilitation program or scheduled follow-up assessments.
Source: ClinicalTrials.gov (NCT07762989). StuddyBuddy aggregates publicly available trial information.