[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"ankle-injuries-and-disorders\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:ankle-injuries-and-disorders":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,45,69,93],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":29,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100576047","phase-2-assessment-of-medrol-dosepak-to-reduce-opioid-consumption-in-foot-and-ankle-surgical-patients-100576047",false,"NCT06780202","Assessment of Medrol Dosepak to Reduce Opioid Consumption in Foot and Ankle Surgical Patients","Inclusion Criteria:\n\n-Emory Orthopedic patients undergoing foot and ankle surgery\n\nExclusion Criteria:\n\n* Concurrent or significant injuries to other bones or organs\n* Local infections\n* History of alcohol or medical abuse, including prior opioid abuse\n* Smoking\n* History of severe heart disease, renal failure, liver dysfunction, active peptic ulcer disease, diabetes, rheumatoid arthritis, neurological or psychiatric diseases that could influence pain perception\n* Pre-existing immune suppression\n* Those deemed possibly non-compliant by the study team and,\n* All vulnerable populations (those unable to give consent, juveniles, pregnant women, prisoners, cognitively impaired and non-English speaking).","ALL","18 Years","95 Years",{"count":19,"type":20},180,"ESTIMATED","INTERVENTIONAL",[23],"PHASE2","This clinical trial aims to determine the effects of a 6-day low-dose methylprednisolone course on pain, nausea, and total opioid consumption in patients undergoing foot and ankle surgeries.\n\nThe secondary objective of the study is to determine and monitor the effects of the course on complications following surgery and patient-reported outcomes",[26,27,28],"Foot Injuries and Disorders","Ankle Injuries and Disorders","Achilles Tendon Injury",[30,31],"VAS scale: visual analog scale","Medrol Dosepak","RECRUITING","2026-03-05",{"date":35,"type":36},"2026-03-09","ACTUAL",{"date":38,"type":36},"2025-01-27",{"date":40,"type":20},"2027-12",{"name":42,"class":43},"Emory University","OTHER",2,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":51,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":53,"targetDuration":4,"studyType":21,"phases":55,"briefSummary":57,"conditions":58,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":64,"leadSponsor":66,"locationsCount":68},"100618708","postoperative-complications-of-ankle-arthroscopy-100618708","NCT07335133","Postoperative Complications of Ankle Arthroscopy","Short- and Medium-term Postoperative Complications of Ankle Arthroscopy","ARTHRO2025","Inclusion Criteria:\n\n* Adult patient who has been informed and has signed the consent form\n* Patient scheduled for arthroscopic ankle surgery.\n* Patient affiliated with or covered by a health insurance plan\n\nExclusion Criteria:\n\n* Recent traumatic injury (less than 1 month old), physical therapy assessment impossible\n* Inability to follow up for up to one year\n* Patient under legal protection\n* Pregnant woman, patient under guardianship or conservatorship\n* Patient who has already undergone ankle surgery",{"count":54,"type":20},150,[56],"NA","The goal of this clinical trial is to describe complications that occurred in the year following surgery, based on follow-up surgical consultations and physical therapy sessions.\n\nThe target population is any adult patient who has undergone ankle surgery performed under arthroscopy.\n\nPrimary outcome is description of all complications occurring within one year following ankle arthroscopy. This description will be based on clinical and functional examinations performed by surgeons and physical therapists.\n\nParticipants will be regularly monitored by the surgeon and physical therapist (15 days postoperative, 3 months, 6 months, and 1 year).\n\nThey will complete self-assessment questionnaires and undergo functional physical therapy tests, including ALR RSI, FAAM AVQ, FAAM Sport, CAIT, and Ankle Go.",[27,59],"Surgery Complications","2026-01-05",{"date":62,"type":36},"2026-01-12",{"date":60,"type":36},{"date":65,"type":20},"2028-06",{"name":67,"class":43},"Clinique Saint Jean, France",1,{"id":70,"slug":71,"hasResults":11,"nctId":72,"briefTitle":73,"officialTitle":74,"acronym":4,"eligibilityCriteria":75,"healthyVolunteers":76,"sex":15,"minAge":16,"maxAge":77,"enrollmentInfo":78,"targetDuration":4,"studyType":21,"phases":80,"briefSummary":81,"conditions":82,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":84,"lastUpdatePostDateStruct":85,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":44},"100582823","auditory-biofeedback-gait-training-individuals-with-chronic-ankle-instability-100582823","NCT06868316","Auditory Biofeedback Gait Training Individuals With Chronic Ankle Instability","Optimizing Retention on Duty in Patients With Chronic Ankle Instability Using Auditory Biofeedback Gait Training: A Multisite Randomized Controlled Trial","Inclusion Criteria:\n\n* Physically active adults (defined as participants reporting a score of =4 on the National Aeronautics and Space Administration (NASA) Activity Instrument and indicating they can run for at least 20 consecutive minutes)\n* History of ankle sprain\n* 2 episodes of \"giving way\" in the past 6-months\n* must answer \"yes\" to =5 questions on the Ankle Instability Instrument (AII) and =11 on the Identification of Functional Ankle Instability (IdFAI)\n\nExclusion Criteria:\n\n* an ankle sprain in the previous four weeks or lower extremity neuromusculoskeletal injury other than to the ankle in the last 12 months\n* history of surgery in the lower extremity\n* fracture to the lower extremity in the past 12 months or a fracture that required open-reduction internal fixation\n* history of neurological disease, vestibular or visual disturbance or any other pathology that would impair sensorimotor performance or gait\n* current participation in a formal ankle joint rehabilitation program\n* a concussion in the last 12 months\n* report a cardiovascular, metabolic, or renal disease, or signs and symptoms that suggest such condition or have been told by a medical provider not to engage in vigorous physical activity (such as running).",true,"45 Years",{"count":79,"type":20},100,[56],"The goal of this randomized clinical controlled trial is examine the effects of gait training with auditory biofeedback (AudFB) on gait biomechanics, clinical measures of ankle joint health, and patient-centered outcomes. The following specific aims will achieve this objective:\n\n* Specific Aim 1: Determine if a 6-week gait training with AudFB intervention improves lower extremity biomechanics compared to a Control condition in participants with CAI.\n* Specific Aim 2: Determine if a 6-week gait training with AudFB reduces talar cartilage deformation compared to a Control condition in participants with CAI.\n* Specific Aim 3: Determine if a 6-week gait training with AudFB reduces episodes of ankle giving-way and reduces self-perceived severity of symptoms relative to a Control condition in participants with CAI.\n\nParticipants will:\n\n* Complete 12 intervention sessions over a 6-week period of walking, ruck marching, and runninig.\n* Complete testing sessions before and after the intervention, then after 6 and 12-months following the intervention.",[83,27],"Ankle Sprains","2025-10-01",{"date":86,"type":36},"2025-10-07",{"date":88,"type":36},"2025-05-27",{"date":90,"type":20},"2028-09",{"name":92,"class":43},"University of Kentucky",{"id":94,"slug":95,"hasResults":11,"nctId":96,"briefTitle":97,"officialTitle":98,"acronym":4,"eligibilityCriteria":99,"healthyVolunteers":76,"sex":15,"minAge":16,"maxAge":100,"enrollmentInfo":101,"targetDuration":4,"studyType":21,"phases":103,"briefSummary":104,"conditions":105,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":107,"lastUpdatePostDateStruct":108,"startDateStruct":110,"completionDateStruct":112,"leadSponsor":114,"locationsCount":68},"100554503","the-effect-of-taping-on-plantar-pressure-distribution-in-players-with-chronic-ankle-instability-100554503","NCT06499935","The Effect of Taping on Plantar Pressure Distribution in Players With Chronic Ankle Instability","The Immediate Effects of Rigid Taping Versus Kinesio-Taping on Plantar Pressure Distribution in Basketball Players With Chronic Ankle Instability","Inclusion Criteria:\n\n* A history of at least 1 significant ankle sprain\n* The initial sprain must have occurred at least 12 months before study enrollment\n* A history of the previously injured ankle joint \"giving way\" and\u002For recurrent sprain and\u002For \"feelings of instability.\"\n* Cumberland Ankle Instability Tool: score of 24 or less\n\nExclusion Criteria:\n\n* A history of previous surgeries to the musculoskeletal structures (i.e., bones, joint structures, nerves) in either lower extremity\n* A history of a fracture in either lower extremity requiring realignment\n* Acute injury to musculoskeletal structures of other joints of the lower extremity in the previous 3 months that impacted joint integrity and function (i.e., sprains, fracture) resulting in at least 1 interrupted day of desired physical activity.","28 Years",{"count":102,"type":20},88,[56],"The goal of this study is to investigate whether there exists a difference in baropdometric readings of plantar pressure between individuals with chronic ankle instability and normal health individuals, in addition another goal of this study is to investigate the effect of rigid taping vs. kinesio taping on plantar pressure distribution as well as stability markers in individuals with chronic ankle instability.\n\nThe main questions aimed to answer are:\n\n1. Is there a difference in plantar pressure distribution between individuals with chronic ankle instability and individuals without chronic ankle instability?\n2. What effect do rigid and kinesio taping have on plantar pressure distribution and ankle stability markers?\n3. Which tape affects plantar pressure distribution and ankle stability better?\n\nParticipants will:\n\nFirstly be divided into two macro groups, one with chronic ankle instability and one without, with an observational part of the study to be carried out to investigate the differences in plantar pressure between both groups.\n\nSecondly, the group with chronic ankle instability will be divided into two micro groups one receiving rigid taping and the other receiving kinesio taping, and the immediate effects of these tapes in terms of plantar pressure and ankle stability will be recorded and compared before and after within groups, and after between both groups.",[106,27,83],"Ankle Injuries","2024-07-07",{"date":109,"type":36},"2024-07-15",{"date":111,"type":36},"2024-05-24",{"date":113,"type":20},"2024-10-25",{"name":115,"class":43},"Cairo University"]