[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"diabetic-foot-osteomyelitis\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:diabetic-foot-osteomyelitis":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,40],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":20,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":28,"lastUpdatePostDateStruct":29,"startDateStruct":32,"completionDateStruct":34,"leadSponsor":36,"locationsCount":39},"100516891","cerament-g-device-registry-100516891",false,"NCT06010433","CERAMENT G Device Registry","Inclusion Criteria:\n\n* 18 years and over (on the day of surgery)\n* receive CERAMENT\\|G as a component of their treatment at a participating, contracted centre or healthcare provider, in accordance with the IFU for the implanted product\n* In receipt of patient information leaflet and have signed appropriately designed informed consent form.\n\nExclusion Criteria:\n\n* Any exclusion criteria as per IFU for CERAMENT\\|G\n* Any off-label use","ALL","18 Years",{"count":18,"type":19},100,"ESTIMATED","12 Months","OBSERVATIONAL","This is an Observational Device Registry Study of CERAMENT\\|G in normal use in accordance with the IFU. It will run for a period of three years from enrolment of the first patient into the Study at each Site, before being subject to review. A Device Registry is a form of observational study that concerns the performance of a device in normal use. It is intended to collect data that is reflective of 'real world' device performance.",[24,25,26],"Chronic Osteomyelitis","Fracture Related Infection","Diabetic Foot Osteomyelitis","RECRUITING","2025-09-23",{"date":30,"type":31},"2025-09-26","ACTUAL",{"date":33,"type":31},"2023-08-17",{"date":35,"type":19},"2028-09-22",{"name":37,"class":38},"BONESUPPORT AB","INDUSTRY",3,{"id":41,"slug":42,"hasResults":11,"nctId":43,"briefTitle":44,"officialTitle":44,"acronym":45,"eligibilityCriteria":46,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":4,"targetDuration":4,"studyType":47,"phases":4,"briefSummary":48,"conditions":49,"keywords":4,"overallStatus":51,"whyStopped":4,"lastUpdateSubmitDate":52,"lastUpdatePostDateStruct":53,"startDateStruct":4,"completionDateStruct":4,"leadSponsor":55,"locationsCount":4},"100578228","expanded-access-program-eap-stimulan-vg-100578228","NCT06808568","Expanded Access Program (EAP) STIMULAN VG","EAPSTIMVG","Inclusion Criteria:\n\n\\-\n\nExclusion Criteria:\n\n\\-","EXPANDED_ACCESS","Individual (single) patient expanded access may be considered.",[50,26],"Stage IV Pressure Ulcer","AVAILABLE","2025-01-29",{"date":54,"type":31},"2025-02-05",{"name":56,"class":38},"Biocomposites Ltd"]