Join us at Health Research Day — June 6th at Canton Waterfront Park, Baltimore!   Learn More →
← Back to all trials
Recruiting 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.

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07762989). StuddyBuddy aggregates publicly available trial information.