[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"ankle-ligaments-instability-old-injury\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:ankle-ligaments-instability-old-injury":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,42,69],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100618603","equisock-new-antiequine-100618603",false,"NCT07333768","EQUISOCK: New Antiequine","EQUISOCK: New Antiequine for Ankle","EQUISOCK","Inclusion Criteria:\n\n* patients with chronic ankle injuries\n* patients with external popliteal sciatic nerve lesion or nerve injuries resulting in loss of ankle dorsiflexion\n* patients who have already been prescribed an orthosis\n* patients of all ages\n\nExclusion Criteria:\n\n* inability to stand actively and stably\n* inability to walk unaided\n* inability to follow instructions","ALL",{"count":19,"type":20},4,"ESTIMATED","INTERVENTIONAL",[23],"NA","The goal of this experimental study is to test the feasibility and validity of a new orthosis in patients with ankle lesions (external popliteal sciatic nerve or nerve injuries resulting in loss of ankle dorsiflexion) of both sexes and all ages. The main question it aims to answer is:Is the new orthosis a support for ankle stability??Does the new orthosis improve ankle function and patients' quality of life??The control group will be the subjects themselves when wearing their conventional ankle orthosis or without it. Participants must wear the new ankle orthosis for at least one month to assess the effectiveness of the orthosis and evaluate any changes that have occurred in the ankle joint and muscles.",[26,27,28],"Ankle (Ligaments); Instability (Old Injury)","Ankle Equinus","Ankle Dorsiflexion","NOT_YET_RECRUITING","2026-04-27",{"date":32,"type":33},"2026-04-28","ACTUAL",{"date":35,"type":20},"2026-07-01",{"date":37,"type":20},"2026-12-31",{"name":39,"class":40},"University of Salamanca","OTHER",1,{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":4,"eligibilityCriteria":48,"healthyVolunteers":11,"sex":17,"minAge":49,"maxAge":50,"enrollmentInfo":51,"targetDuration":4,"studyType":21,"phases":53,"briefSummary":54,"conditions":55,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":4},"100628336","comparison-of-anesthetic-techniques-for-early-recovery-after-ankle-arthroscopy-100628336","NCT07460310","Comparison of Anesthetic Techniques for Early Recovery After Ankle Arthroscopy","Comparison of Total Intravenous, Balanced, and Spinal Anesthesia for Early Recovery Following Ankle Arthroscopy: A Multicenter, Prospective, Randomized Controlled Trial.","Inclusion Criteria:\n\n* Full understanding of the study procedures and methods, with a signed written informed consent form.\n* Aged 18 to 65 years, of either sex.\n* Scheduled for elective unilateral minimally invasive ankle surgery.\n* American Society of Anesthesiologists (ASA) physical status classification I or II.\n* Body Mass Index (BMI) between 16 and 32 kg\u002Fm\\^2\n\nExclusion Criteria:\n\n* Known hypersensitivity or allergy to any study medications or existing contraindications to anesthesia.\n* Chronic obstructive pulmonary disease (COPD) or unstable asthma.\n* History of difficult airway management, poorly controlled gastroesophageal reflux disease (GERD), or a known risk of aspiration.\n* Anticipated surgical duration exceeding 3 hours.\n* History of chronic preoperative opioid use or dependence.\n* History of severe postoperative adverse reactions (e.g., severe postoperative nausea and vomiting).\n* Pregnancy or lactation.\n* History of seizure disorders or epilepsy.\n* Severe peripheral neuropathy.\n* Any other condition that, in the opinion of the investigator, would preclude safe participation in the study.","18 Years","65 Years",{"count":52,"type":20},200,[23],"Ankle arthroscopy is increasingly performed as a day-case procedure, making rapid recovery and efficient discharge critical. Anesthetic technique substantially influences postoperative recovery, yet high-quality evidence comparing anesthetic strategies in ankle arthroscopy is limited.\n\nThis multicenter randomized trial compares total intravenous anesthesia with propofol plus peripheral nerve block (PNB), general anesthesia plus PNB, and spinal anesthesia, with PACU-I recovery time as the primary outcome. Secondary outcomes include postoperative pain, opioid consumption, hospital length of stay, adverse events, recovery quality, satisfaction, limb weakness, and intraoperative hemodynamics.",[56,26,57,58,59],"Ankle Sprain","Pain Management","ERAS","Ankle Arthroscopy","2026-03-04",{"date":62,"type":33},"2026-03-10",{"date":64,"type":20},"2026-03-01",{"date":66,"type":20},"2026-12-30",{"name":68,"class":40},"Second Affiliated Hospital, School of Medicine, Zhejiang University",{"id":70,"slug":71,"hasResults":11,"nctId":72,"briefTitle":73,"officialTitle":74,"acronym":75,"eligibilityCriteria":76,"healthyVolunteers":11,"sex":17,"minAge":77,"maxAge":4,"enrollmentInfo":78,"targetDuration":80,"studyType":81,"phases":4,"briefSummary":82,"conditions":83,"keywords":87,"overallStatus":99,"whyStopped":4,"lastUpdateSubmitDate":100,"lastUpdatePostDateStruct":101,"startDateStruct":103,"completionDateStruct":105,"leadSponsor":107,"locationsCount":41},"100607423","french-ankle-ligament-surgery-cohort-study-100607423","NCT07188363","French Ankle Ligament Surgery Cohort Study","Prospective Follow-up Study of Patients Undergoing Ankle Ligament Surgery","AnkleCDS","Inclusion Criteria:\n\n* Retensioning, ankle ligament reconstruction or syndesmosis repair surgery\n\nExclusion Criteria:\n\n* Patient refusal","7 Years",{"count":79,"type":20},5000,"20 Years","OBSERVATIONAL","This 20-year cohort study foolows patients after ankle ligament reconstruction surgery to evaluate re-rupture rates, long term functional outcomes, return to sport rates ans complications? The goal is to provide insights into the procedure's durability and effectiveness to enhance patient care.",[26,84,85,86],"Ankle Ligament Rupture","Ankle Instability","Syndesmotic Injury",[88,89,90,91,92,93,94,95,96,97,98],"ankle","ligamentoplasty","surgery","orthopedy","FHL","rupture","ligament","syndesmosis","instability","retensioning","flexor hallucic longus","RECRUITING","2026-01-03",{"date":102,"type":33},"2026-01-06",{"date":104,"type":33},"2022-09-01",{"date":106,"type":20},"2062-08-30",{"name":108,"class":40},"Chirurgie Du Sport"]