[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100651733":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":19,"centralContacts":24,"locations":10,"responsibleParty":32,"collaborators":10,"id":34,"slug":35,"hasResults":36,"nctId":37,"briefTitle":38,"officialTitle":38,"acronym":39,"eligibilityCriteria":40,"healthyVolunteers":36,"sex":41,"minAge":42,"maxAge":10,"enrollmentInfo":43,"targetDuration":10,"studyType":46,"phases":10,"briefSummary":47,"conditions":48,"keywords":10,"overallStatus":55,"whyStopped":10,"lastUpdateSubmitDate":56,"lastUpdatePostDateStruct":57,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":64,"locationsCount":10},{"fullName":5,"class":6},"Stryker Trauma and Extremities","INDUSTRY",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Tornier Perform™ Reversed MonoPost",null,"The Commercially available Tornier Perform™ Reversed MonoPost Glenoid is intended to replace the glenoid part of the scapulohumeral joint as part of a reverse shoulder prosthesis. The Tornier Perform™ Reversed MonoPost Glenoid includes new range of glenoid baseplates for Bony Increased Offset -Reversed Shoulder Arthroplasty (BIO-RSA) and a new range of glenoid baseplates with metallic augmentation to accommodate specific patterns of glenoid wear in patients.",[13],"Device: Tornier Perform™ Reversed MonoPost",[15],{"type":16,"name":9,"description":17,"armGroupLabels":18,"otherNames":10},"DEVICE","The Commercially available Tornier Perform™ Reversed MonoPost Glenoid is intended to replace the glenoid part of the scapulohumeral joint as part of a reverse shoulder prosthesis.",[9],[20],{"name":21,"affiliation":22,"role":23},"Rebecca Gibson","Stryker Trauma & Extremities","STUDY_DIRECTOR",[25,30],{"name":26,"role":27,"phone":28,"phoneExt":10,"email":29},"Monica Fleeman","CONTACT","251-465-5969","Monica.Fleeman@stryker.com",{"name":21,"role":27,"phone":10,"phoneExt":10,"email":31},"Rebecca.Gibson@stryker.com",{"type":33,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100651733","tornier-perform-reversed-monopost-study-100651733",false,"NCT07764614","Tornier Perform™ Reversed Monopost Study","Monarch","Inclusion Criteria:\n\n* 18 years or older at the time of the informed consent.\n* Informed and willing to sign an informed consent form (ICF) approved by Institutional Review Board (IRB) or Ethics Committee (EC).\n* Willing and able to comply with the requirements of the study protocol\n* Considered a candidate or having received shoulder arthroplasty with the device, having a functional deltoid muscle and with massive and non-repairable rotator cuff tear with pain disabled by:\n\n  * Rheumatoid arthritis\n  * Non-inflammatory degenerative joint disease (i.e. osteoarthritis and avascular necrosis)\n  * Correction of functional deformity\n  * Fracture of the Humeral Head\n  * Traumatic arthritis\n  * Revision of the devices if sufficient bone stock remains\n* Enrollment occurred up to 1 year after date of surgery provided that mandatory data are accessible: including ASES, Constant, and Active ROM.\n\nExclusion Criteria:\n\n* Contraindications or hypersensitivity to the use of the Tornier Perform™ Reversed MonoPost System or their components (e.g., metal sensitivity).\n* Participation in the treatment period of another clinical trial during the clinical investigation.\n* Any subject that meets the definition of a Vulnerable Subject per ISO 14155 Section 3.44. Examples include any subject \"with lack of or loss of autonomy due to immaturity or through mental disability, persons in nursing homes, children, impoverished","ALL","18 Years",{"count":44,"type":45},150,"ESTIMATED","OBSERVATIONAL","This study is a Multi-center, Prospective Follow-up, Non-significant risk, Post-Market Clinical Follow-Up (PMCF) study to Evaluate the Safety and Effectiveness of the Tornier Perform™ Reversed MonoPost System.",[49,50,51,52,53,54],"Non-inflammatory Degenerative Joint Disease","Rhematoid Arthritis","Correction of Functional Deformity","Fracture of the Humeral Head","Traumatic Arthritis","Revision of the Devices if Sufficient Bone Stock Remains","NOT_YET_RECRUITING","2026-08-19",{"date":58,"type":59},"2026-08-21","ACTUAL",{"date":61,"type":45},"2026-09-28",{"date":63,"type":45},"2031-08-30",{"name":5,"class":6}]