[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100618614":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":25,"centralContacts":30,"locations":36,"responsibleParty":48,"collaborators":25,"id":52,"slug":53,"hasResults":54,"nctId":55,"briefTitle":56,"officialTitle":57,"acronym":58,"eligibilityCriteria":59,"healthyVolunteers":54,"sex":60,"minAge":61,"maxAge":25,"enrollmentInfo":62,"targetDuration":25,"studyType":65,"phases":66,"briefSummary":68,"conditions":69,"keywords":25,"overallStatus":72,"whyStopped":25,"lastUpdateSubmitDate":73,"lastUpdatePostDateStruct":74,"startDateStruct":77,"completionDateStruct":79,"leadSponsor":81,"locationsCount":82},{"fullName":5,"class":6},"University of Salamanca","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Orlint-Orlext orthosis group","EXPERIMENTAL","Participants must wear the new knee orthosis during assessments and in their daily lives for at least one month, which is the duration of the study.",[13],"Device: Orlint-Orlext orthosis device",{"label":15,"type":16,"description":17,"interventionNames":18},"Conventional orthesis group","ACTIVE_COMPARATOR","Participants must wear the conventional knee orthosis (a without orthosis) during assessments and in their daily lives, before wear the new one.",[19],"Device: Conventional orthosis device",[21,26],{"type":22,"name":23,"description":11,"armGroupLabels":24,"otherNames":25},"DEVICE","Orlint-Orlext orthosis device",[9],null,{"type":22,"name":27,"description":28,"armGroupLabels":29,"otherNames":25},"Conventional orthosis device","Participants must wear the conventional knee orthosis and without orthosis, during assessments and before wearing the new one",[15],[31],{"name":32,"role":33,"phone":34,"phoneExt":25,"email":35},"Rocío Llamas-Ramos Dr.","CONTACT","+3465785488","rociollamas@usal.es",[37],{"facility":5,"status":25,"city":38,"state":38,"zip":39,"country":40,"countryCode":41,"cosmosGeoPoint":42,"geoPoint":47,"contacts":25},"Salamanca","37007","Spain","ES",{"type":43,"coordinates":44},"Point",[45,46],-5.66388,40.96882,{"lat":46,"lon":45},{"type":49,"investigatorFullName":50,"investigatorTitle":51,"investigatorAffiliation":5,"oldNameTitle":25,"oldOrganization":25},"PRINCIPAL_INVESTIGATOR","Rocío Llamas-Ramos","Principal Investigator","100618614","orlint--orlext-orthosis-for-knee-100618614",false,"NCT07333911","ORLINT & ORLEXT: Orthosis for Knee","ORLINT & ORLEXT: New Orthosis for the Lateral Knee Ligaments","ORLINT&ORLEXT","Inclusion Criteria:\n\n* patients with chronic knee injuries\n* patients who have already been prescribed an orthosis\n* patients older than 18 years old\n\nExclusion Criteria:\n\n* inability to stand actively and stably\n* inability to walk unaided","ALL","18 Years",{"count":63,"type":64},4,"ESTIMATED","INTERVENTIONAL",[67],"NA","The goal of this experimental study is to test the feasibility and validity of a new orthosis in patients with lateral ligament knee lesions of both sexes and older than 18 years old. The main question it aims to answer is:\n\nIs the new orthosis a support for knee stability?? Does the new orthosis improve knee function and patients' quality of life??\n\nThe control group will be the subjects themselves when wearing their conventional knee orthosis or without it.\n\nParticipants must wear the new knee orthosis for at least one month to assess the effectiveness of the orthosis and evaluate any changes that have occurred in the knee joint and muscles.",[70,71],"Knee Brace","Knee","NOT_YET_RECRUITING","2026-04-27",{"date":75,"type":76},"2026-04-28","ACTUAL",{"date":78,"type":64},"2026-07-01",{"date":80,"type":64},"2026-12-31",{"name":5,"class":6},1]