[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100637974":3},{"organization":4,"armGroups":7,"interventions":18,"overallOfficials":10,"centralContacts":27,"locations":36,"responsibleParty":93,"collaborators":10,"id":95,"slug":96,"hasResults":97,"nctId":98,"briefTitle":99,"officialTitle":100,"acronym":10,"eligibilityCriteria":101,"healthyVolunteers":97,"sex":102,"minAge":10,"maxAge":10,"enrollmentInfo":103,"targetDuration":10,"studyType":106,"phases":10,"briefSummary":107,"conditions":108,"keywords":110,"overallStatus":115,"whyStopped":10,"lastUpdateSubmitDate":116,"lastUpdatePostDateStruct":117,"startDateStruct":120,"completionDateStruct":122,"leadSponsor":124,"locationsCount":125},{"fullName":5,"class":6},"Globus Medical Inc","INDUSTRY",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"4.0 Group",null,"4.0 mm diameter REFLECT cords were used to treat patients.",[13],"Device: Scoliosis Correction System",{"label":15,"type":10,"description":16,"interventionNames":17},"5.0 Group","5.0 mm diameter REFLECT cords were used to treat patients.",[13],[19,24],{"type":20,"name":21,"description":22,"armGroupLabels":23,"otherNames":10},"DEVICE","Scoliosis Correction System","The REFLECT system is a non-fusion spinal device, meaning it corrects scoliosis without permanently fusing the spine. Instead of rigid metal rods, it uses a flexible polymer cord attached to screws. For this intervention, a 4.0 mm cord diameter was used to treat patients.",[9],{"type":20,"name":21,"description":25,"armGroupLabels":26,"otherNames":10},"The REFLECT system is a non-fusion spinal device, meaning it corrects scoliosis without permanently fusing the spine. Instead of rigid metal rods, it uses a flexible polymer cord attached to screws. For this intervention, a 5.0 mm cord diameter was used to treat patients.",[15],[28,33],{"name":29,"role":30,"phone":31,"phoneExt":10,"email":32},"Rebecca Smith","CONTACT","858-922-7112","rsmith@globusmedical.com",{"name":34,"role":30,"phone":10,"phoneExt":10,"email":35},"Shannon Bahn","sbahn@globusmedical.com",[37,57,75],{"facility":38,"status":10,"city":39,"state":39,"zip":40,"country":41,"countryCode":42,"cosmosGeoPoint":43,"geoPoint":48,"contacts":49},"NYU Langone Orthopedic Center","New York","11554","United States","US",{"type":44,"coordinates":45},"Point",[46,47],-74.00597,40.71427,{"lat":47,"lon":46},[50,54],{"name":51,"role":30,"phone":52,"phoneExt":10,"email":53},"Korine Pagulayan","516-324-7500","korine.pagulayan@nyulangone.org",{"name":55,"role":56,"phone":10,"phoneExt":10,"email":10},"Juan C Rodriguez-Olaverri, MD, PhD","PRINCIPAL_INVESTIGATOR",{"facility":58,"status":10,"city":59,"state":59,"zip":60,"country":61,"countryCode":62,"cosmosGeoPoint":63,"geoPoint":67,"contacts":68},"Eifel Clinic St. Brigida GmbH & Co. KG","Simmerath","52152","Germany","DE",{"type":44,"coordinates":64},[65,66],6.3,50.6,{"lat":66,"lon":65},[69,73],{"name":70,"role":30,"phone":71,"phoneExt":10,"email":72},"Mahmoud Alkharsawi, MD","+41 02473 89-2325","m.alkharsawi@gmail.com",{"name":74,"role":56,"phone":10,"phoneExt":10,"email":10},"Per Trobisch, MD",{"facility":76,"status":10,"city":77,"state":78,"zip":79,"country":80,"countryCode":10,"cosmosGeoPoint":81,"geoPoint":85,"contacts":86},"Acibadem Maslak Hospital","Istanbul","I","34457","Turkey (Türkiye)",{"type":44,"coordinates":82},[83,84],28.94966,41.01384,{"lat":84,"lon":83},[87,91],{"name":88,"role":30,"phone":89,"phoneExt":10,"email":90},"Tais Zulemyan","+90 212 304 36 36","tais.zulemyan@gmail.com",{"name":92,"role":56,"phone":10,"phoneExt":10,"email":10},"Ahmet Alanay, MD",{"type":94,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100637974","a-retrospective-review-outcomes-of-the-reflect-system-for-idiopathic-scoliosis-100637974",false,"NCT07589023","A Retrospective Review: Outcomes of the REFLECT™ System for Idiopathic Scoliosis","A Retrospective Review of Clinical and Radiographic Outcomes Following the Use of the REFLECT™ Scoliosis Correction System in the Treatment of Idiopathic Scoliosis","Inclusion Criteria:\n\nSubjects must meet all of the following criteria to be included in the study:\n\n1. Requires surgical treatment to obtain and maintain correction of idiopathic scoliosis\n2. Skeletally immature\n3. Major Cobb angle of 30° and 65°\n4. Bone structure adequate to safely accommodate screw fixation\n5. Failed bracing treatment and\u002For intolerant to brace wear\n6. Treated with the REFLECT™ Scoliosis Correction System, using single or dual REFLECT cord(s) per curve\n7. Availability of medical and radiographic records evaluating the product under study preoperatively through a minimum of 12 months postoperative\n\nExclusion Criteria:\n\nPatients were excluded from the study if they met any of the following conditions:\n\n1. Presence of any systemic infection, local infection, or skin compromise at the surgical site\n2. Prior spinal surgery at the level(s) to be treated\n3. Known poor bone quality, defined as a T-score of -1.5 or less\n4. Any other medical or surgical condition which would preclude the potential benefit of spinal surgery, such as coagulation disorders, allergies to the implant materials, or patient unwillingness or inability to cooperate with postoperative care instructions","ALL",{"count":104,"type":105},100,"ESTIMATED","OBSERVATIONAL","This study reviews medical records of children and adolescents treated for idiopathic scoliosis (a sideways curve of the spine with no known cause) using the REFLECT™ Scoliosis Correction System.",[109],"Idiopathic Scoliosis",[111,112,113,114],"scoliosis","idiopathic scoliosis","spinal curve","REFLECT System","NOT_YET_RECRUITING","2026-05-11",{"date":118,"type":119},"2026-05-15","ACTUAL",{"date":121,"type":105},"2026-06-15",{"date":123,"type":105},"2027-07-31",{"name":5,"class":6},3]