[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100539051":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":20,"centralContacts":21,"locations":30,"responsibleParty":61,"collaborators":20,"id":63,"slug":64,"hasResults":65,"nctId":66,"briefTitle":67,"officialTitle":68,"acronym":20,"eligibilityCriteria":69,"healthyVolunteers":65,"sex":70,"minAge":20,"maxAge":20,"enrollmentInfo":71,"targetDuration":20,"studyType":74,"phases":75,"briefSummary":77,"conditions":78,"keywords":20,"overallStatus":33,"whyStopped":20,"lastUpdateSubmitDate":80,"lastUpdatePostDateStruct":81,"startDateStruct":84,"completionDateStruct":86,"leadSponsor":88,"locationsCount":89},{"fullName":5,"class":6},"Globus Medical Inc","INDUSTRY",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"REFLECT","OTHER","Enrolled patients are treated with the REFLECT Scoliosis System. This is an HDE-approved device.",[13],"Device: REFLECT Scoliosis Correction System",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"DEVICE","REFLECT Scoliosis Correction System","The REFLECT™ Scoliosis Correction System is designed for continued growth and mobility of the spine as well as straightening of the spine by holding the segments in a more natural anatomic position using non-rigid materials.",[9],null,[22,27],{"name":23,"role":24,"phone":25,"phoneExt":20,"email":26},"Rebecca Smith","CONTACT","858-922-7112","rsmith@globusmedical.com",{"name":28,"role":24,"phone":20,"phoneExt":20,"email":29},"Shannon Bahn","sbahn@globusmedical.com",[31,51],{"facility":32,"status":33,"city":34,"state":35,"zip":36,"country":37,"countryCode":38,"cosmosGeoPoint":39,"geoPoint":44,"contacts":45},"Mayo Clinic","RECRUITING","Rochester","Minnesota","55905","United States","US",{"type":40,"coordinates":41},"Point",[42,43],-92.4699,44.02163,{"lat":43,"lon":42},[46,48],{"name":47,"role":24,"phone":20,"phoneExt":20,"email":20},"Angie Severson",{"name":49,"role":50,"phone":20,"phoneExt":20,"email":20},"Noelle Larson, MD","PRINCIPAL_INVESTIGATOR",{"facility":52,"status":53,"city":54,"state":54,"zip":55,"country":37,"countryCode":38,"cosmosGeoPoint":56,"geoPoint":60,"contacts":20},"New York University","ENROLLING_BY_INVITATION","New York","10016",{"type":40,"coordinates":57},[58,59],-74.00597,40.71427,{"lat":59,"lon":58},{"type":62,"investigatorFullName":20,"investigatorTitle":20,"investigatorAffiliation":20,"oldNameTitle":20,"oldOrganization":20},"SPONSOR","100539051","reflect-scoliosis-system-post-approval-study-100539051",false,"NCT06298812","REFLECT Scoliosis System Post Approval Study","A Prospective, Single-Arm, Multi-Center, Registry Post-Approval Study of Growth Modulation in the Treatment of Idiopathic Scoliosis With the REFLECT™ Scoliosis Correction System","Inclusion Criteria:\n\n* Diagnosis of progressive idiopathic scoliosis\n* Preoperative major Cobb angle 30°-65°\n* Preoperative flexibility to ≤30° on side bending radiograph (left or right)\n* Skeletally immature at the time of surgery with Risser sign \\\u003C5 or Sanders score \\\u003C8\n* Osseous structure dimensionally adequate to accommodate screw fixation, as determined by radiographic imaging\n* Failed or intolerant to bracing\n* Signed informed consent and\u002For assent forms specific to this study\n\nExclusion Criteria:\n\n* Prior spinal surgery at the level(s) to be treated\n* Documented poor bone quality, defined as a T-score of -1.5 or less\n* Presence of any systemic infection, local infection, or skin compromise at the surgical site\n* Any medical or surgical condition which would preclude the potential benefit of spinal surgery, such as coagulation disorders, allergies to the implant materials, and patient's unwillingness or inability to cooperate with post-operative care instructions\n* Unwillingness, inability, or living situation (e.g. custody arrangements, homelessness, detention) that would preclude ability to return to the study site for follow-up visits as described in protocol and Informed Consent\n* Active participation in a drug or device study that is more than minimal risk such that participation would confound the measurements of the present study","ALL",{"count":72,"type":73},100,"ESTIMATED","INTERVENTIONAL",[76],"NA","The purpose of this multi-center, prospective, single-arm registry Post-Approval Study (PAS) is to evaluate the radiographic and clinical outcomes of 100 patients with idiopathic scoliosis treated with the REFLECT™ Scoliosis Correction System, as a condition of HDE approval",[79],"Idiopathic Scoliosis","2026-02-11",{"date":82,"type":83},"2026-02-13","ACTUAL",{"date":85,"type":83},"2024-04-08",{"date":87,"type":73},"2032-03-31",{"name":5,"class":6},2]