[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100408660":3},{"organization":4,"armGroups":7,"interventions":17,"overallOfficials":10,"centralContacts":23,"locations":33,"responsibleParty":50,"collaborators":52,"id":56,"slug":57,"hasResults":58,"nctId":59,"briefTitle":60,"officialTitle":61,"acronym":62,"eligibilityCriteria":63,"healthyVolunteers":58,"sex":64,"minAge":65,"maxAge":66,"enrollmentInfo":67,"targetDuration":10,"studyType":70,"phases":10,"briefSummary":71,"conditions":72,"keywords":10,"overallStatus":36,"whyStopped":10,"lastUpdateSubmitDate":80,"lastUpdatePostDateStruct":81,"startDateStruct":84,"completionDateStruct":86,"leadSponsor":88,"locationsCount":89},{"fullName":5,"class":6},"University of Colorado, Denver","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Patients with Personalized SpineRods",null,"The patient is being treated with the patient-specific rod with a surgery date planned",[13],"Device: Patient Specific Rod",{"label":15,"type":10,"description":16,"interventionNames":10},"Patient with other hardware","Patients with other hardware not patient-specific",[18],{"type":19,"name":20,"description":21,"armGroupLabels":22,"otherNames":10},"DEVICE","Patient Specific Rod","Posterior spinal fusion rod",[9],[24,29],{"name":25,"role":26,"phone":27,"phoneExt":10,"email":28},"Christopher Kleck, MD","CONTACT","720-848-1900","Christopher.Kleck@CUAnschutz.edu",{"name":30,"role":26,"phone":31,"phoneExt":10,"email":32},"jiandong hao","303-724-7457","jiandong.hao@cuanschutz.edu",[34],{"facility":35,"status":36,"city":37,"state":38,"zip":39,"country":40,"countryCode":41,"cosmosGeoPoint":42,"geoPoint":47,"contacts":48},"Dr. Christopher Kleck, MD","RECRUITING","Aurora","Colorado","80045","United States","US",{"type":43,"coordinates":44},"Point",[45,46],-104.83192,39.72943,{"lat":46,"lon":45},[49],{"name":30,"role":26,"phone":31,"phoneExt":10,"email":32},{"type":51,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR",[53],{"name":54,"class":55},"Personalized Spine Study Group","UNKNOWN","100408660","personalized-spine-study-group-pssg-registry-100408660",false,"NCT04601363","Personalized Spine Study Group (PSSG) Registry","Personalized Spine Study Group (PSSG) Registry of Patients With Personalized Spine Rod Implantation","PSSG","Inclusion Criteria:\n\n* Patient has been\u002F will be operated and instrumented with patient-specific rod or spine hardware (control cohort)\n* Patient able to consent or assent\n\nExclusion Criteria:\n\n* Patient unable to sign an informed consent form\n* Patient unable to complete a self-administered questionnaire\n* Patient is pregnant or planning on becoming pregnant during the duration of their study participation\n* Patient is older than 85\n* Patient is younger than 10","ALL","10 Years","85 Years",{"count":68,"type":69},1000,"ESTIMATED","OBSERVATIONAL","The primary objective of the study is a data collection initiative. The study will collect clinical and radiographic outcomes of patients implanted with patient specific rods. The secondary objective is to collect clinical and radiographic outcomes of patients with hardware as a control cohort to the patient-specific rods.",[73,74,75,76,77,78,79],"Scoliosis; Adolescence","Degenerative Disc Disease","Spinal Fusion","Kyphoscoliosis","Pseudoarthrosis of Spine","Spinal Stenosis","Kyphoses, Scheuermann","2024-10-01",{"date":82,"type":83},"2024-10-03","ACTUAL",{"date":85,"type":83},"2020-10-29",{"date":87,"type":69},"2030-04",{"name":5,"class":6},1]