[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Stryker Orthopaedics\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":38},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":10,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":20,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":4,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":27,"lastUpdatePostDateStruct":28,"startDateStruct":31,"completionDateStruct":32,"leadSponsor":34,"locationsCount":37},"100642396",false,"NCT07647354","Mako-MORE Registry","A Prospective, Multi-center, Post-market, Registry-based Evaluation of the Clinical Outcomes in Patients Receiving a Stryker Implant With Use of the Mako Robotic-Arm Assisted System (Mako-MORE)","Inclusion Criteria:\n\n* The subject is skeletally mature, and ≥ 18 years old.\n* The Subject has signed and dated an IRB\u002FEC approved, study specific Informed Patient Consent Form (ICF).\n* The subject is scheduled to undergo manual arthroplasty or Mako Robotic-Arm Assisted Arthroplasty according to IFU.\n* The subject is willing and able to comply with postoperative scheduled clinical evaluations.\n\nExclusion Criteria:\n\n* The subject is not able to express his\u002Fher consent as deemed by the investigator.\n* The subject is not able to fulfill a self-assessment questionnaire or follow-up visits as deemed by the investigator.\n* The subject is a prisoner.\n* Per surgeon discretion the subject is not a candidate for the study.\n* The subject is pregnant or breastfeeding.","ALL","18 Years",{"count":18,"type":19},950,"ESTIMATED","5 Years","OBSERVATIONAL","This is a prospective, post-market, multi-center, registry-based observational study designed to collect real-world clinical data on patients undergoing joint arthroplasty with Stryker implants, with or without the use of the Mako Robotic-Arm Assisted System. The registry will collect prospective data on patient characteristics, procedural details, patient-reported outcomes, radiographic assessments, and adverse events. Patients will be enrolled into procedure-specific cohorts and followed for up to five years postoperatively.",[24,25],"Arthropathy of Knee","Arthropathy of Hip","NOT_YET_RECRUITING","2026-06-09",{"date":29,"type":30},"2026-06-15","ACTUAL",{"date":29,"type":19},{"date":33,"type":19},"2037-03-15",{"name":35,"class":36},"Stryker Orthopaedics","INDUSTRY",5,""]