[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100651617":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":20,"centralContacts":27,"locations":32,"responsibleParty":48,"collaborators":10,"id":51,"slug":52,"hasResults":53,"nctId":54,"briefTitle":55,"officialTitle":56,"acronym":10,"eligibilityCriteria":57,"healthyVolunteers":53,"sex":58,"minAge":59,"maxAge":60,"enrollmentInfo":61,"targetDuration":10,"studyType":64,"phases":10,"briefSummary":65,"conditions":66,"keywords":70,"overallStatus":78,"whyStopped":10,"lastUpdateSubmitDate":79,"lastUpdatePostDateStruct":80,"startDateStruct":83,"completionDateStruct":85,"leadSponsor":87,"locationsCount":88},{"fullName":5,"class":6},"Gazi University","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Peroneus Longus Tendon Autograft ACLR Cohort",null,"Adults after primary unilateral ACL reconstruction using a peroneus longus tendon autograft. Participants will undergo observational assessments at postoperative 6-8 weeks, 3 months, and 6 months. Donor-limb measures will be compared with measurements from the contralateral non-donor limb. No intervention is assigned by the study.",[13],"Procedure: Anterior Cruciate Ligament Reconstruction Using a Peroneus Longus Tendon Autograft",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":10},"PROCEDURE","Anterior Cruciate Ligament Reconstruction Using a Peroneus Longus Tendon Autograft","Participants undergo primary anterior cruciate ligament reconstruction using a peroneus longus tendon autograft as part of their routine clinical care. The graft choice and surgical procedure are determined by the treating orthopedic surgeon independently of study participation. The study does not assign or modify the graft choice, surgical technique, or postoperative rehabilitation. Participants receive routine postoperative rehabilitation according to their clinical needs, while donor-ankle sensorimotor recovery is assessed prospectively at 6-8 weeks, 3 months, and 6 months after surgery.",[9],[21,24],{"name":22,"affiliation":5,"role":23},"Dudu Ozdemir Can, Msc","PRINCIPAL_INVESTIGATOR",{"name":25,"affiliation":5,"role":26},"Nihan Karatas, Prof. Dr.","STUDY_DIRECTOR",[28],{"name":22,"role":29,"phone":30,"phoneExt":10,"email":31},"CONTACT","+90 5534448492","duduozdemir@gazi.edu.tr",[33],{"facility":34,"status":10,"city":35,"state":36,"zip":37,"country":38,"countryCode":10,"cosmosGeoPoint":39,"geoPoint":44,"contacts":45},"Gazi University Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation, Sports Health Unit","Çankaya","Ankara","06490","Turkey (Türkiye)",{"type":40,"coordinates":41},"Point",[42,43],32.86268,39.9179,{"lat":43,"lon":42},[46],{"name":47,"role":29,"phone":30,"phoneExt":10,"email":31},"Dudu Ozdemir Can, MSc",{"type":23,"investigatorFullName":49,"investigatorTitle":50,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"Dudu Özdemir","PhD Candidate, Department of Physiotherapy and Rehabilitation","100651617","donor-ankle-sensorimotor-recovery-after-acl-reconstruction-with-a-peroneus-longus-tendon-autograft-100651617",false,"NCT07762989","Donor Ankle Sensorimotor Recovery After ACL Reconstruction With a Peroneus Longus Tendon Autograft","Recovery of Donor Ankle Sensorimotor Function Following Anterior Cruciate Ligament Reconstruction Using Peroneus Longus Tendon Autograft: A Prospective Longitudinal Study","Inclusion Criteria:\n\n* Age 18 to 55 years.\n* Unilateral primary anterior cruciate ligament tear confirmed by clinical examination and magnetic resonance imaging.\n* Primary anterior cruciate ligament reconstruction performed using a peroneus longus tendon autograft.\n* Able and willing to attend the postoperative assessments at 6-8 weeks, 3 months, and 6 months.\n* Written informed consent provided before study participation.\n\nExclusion Criteria:\n\n* Multiligament knee injury.\n* Previous surgery on the index knee or donor ankle.\n* Pre-existing ankle instability or major foot or ankle pathology.\n* Neurological or neuromuscular disease.\n* Inflammatory or systemic disease that may affect the assessments.\n* Major lower-extremity deformity that may affect the assessments.\n* Unable to complete the postoperative rehabilitation program or scheduled follow-up assessments.","ALL","18 Years","55 Years",{"count":62,"type":63},20,"ESTIMATED","OBSERVATIONAL","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.",[67,68,69],"Anterior Cruciate Ligament Injury","Anterior Cruciate Ligament Reconstruction","Donor Site Complication",[71,72,73,74,75,76,77],"peroneus longus tendon autograft","donor ankle","sensorimotor function","surface electromyography","postural control","proprioception","gait analysis","NOT_YET_RECRUITING","2026-08-10",{"date":81,"type":82},"2026-08-13","ACTUAL",{"date":84,"type":63},"2026-08-22",{"date":86,"type":63},"2027-10-01",{"name":5,"class":6},1]