[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Groupe SEBBIN\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":55},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,38],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":4,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":27,"lastUpdatePostDateStruct":28,"startDateStruct":31,"completionDateStruct":33,"leadSponsor":35,"locationsCount":5},"100444077","sebbin-round-anatomical-and-biconvex-gluteal-implants-100444077",false,"NCT05062733","SEBBIN Round, Anatomical and Biconvex Gluteal Implants","Prospective Observational Study About SEBBIN Gluteal Implants","Inclusion Criteria:\n\n* The patient is a man or a woman ≥ 18 years old at the time of inclusion.\n* The patient is planned for a unilateral or bilateral gluteal implant placement with SEBBIN implants as per investigator decision\n* The patient has been informed of the study, has read the patient informed consent and provided consent for the study in writing.\n\nExclusion Criteria:\n\n* Patient implanted with silicone implants somewhere else in the body.\n* Patient candidate for implantation with custom-designed implants.\n* Participation in another interventional clinical study (participation into an observational study is permitted) with a medicinal product or a medical device in the 30 days prior to enrolment.","ALL","18 Years",{"count":19,"type":20},60,"ESTIMATED","OBSERVATIONAL","This study is part of the clinical evaluation of SEBBIN silicone gel-filled gluteal implants, included in the technical file of the device. The aim of the study is to gather additional data about the safety and effectiveness of the device.",[24,25],"Complication","Prosthesis Durability","RECRUITING","2024-10-30",{"date":29,"type":30},"2024-10-31","ACTUAL",{"date":32,"type":30},"2021-11-20",{"date":34,"type":20},"2035-03",{"name":36,"class":37},"Groupe SEBBIN","INDUSTRY",{"id":39,"slug":40,"hasResults":11,"nctId":41,"briefTitle":42,"officialTitle":43,"acronym":4,"eligibilityCriteria":44,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":45,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":47,"conditions":48,"keywords":4,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":27,"lastUpdatePostDateStruct":49,"startDateStruct":50,"completionDateStruct":52,"leadSponsor":54,"locationsCount":5},"100436838","sebbin-silicone-gel-filled-testicular-implants-100436838","NCT04968470","SEBBIN Silicone Gel-filled Testicular Implants","Prospective Observational Study About SEBBIN Silicone Gel-filled Testicular Implants","Inclusion Criteria:\n\n* The patient is an adult or a child at the time of implant placement with SEBBIN implant.\n* The patient is candidate to a unilateral or bilateral testicular implant placement with SEBBIN implant.\n* The patient has been informed of the study, has read the patient information letter and -provided oral consent.\n\nExclusion Criteria:\n\n* The patient has silicone implants somewhere else than in the scrotal sac.\n* The patient was diagnosed with one of the following pathologies:\n\n  * Systemic lupus erythematous, Sjogren syndrome, scleroderma, polymyositis, or any other connective tissue disease.\n  * Rheumatoid arthritis, crystalline arthritis, infectious arthritis, spondyloarthropathies, or any other inflammatory arthritic disease.\n  * Arthritis, fibromyalgia, chronic fatigue syndrome, or any other mechanic or degenerative non-inflammatory rheumatic disease.\n* The patient has a pathology that could delay healing.\n* Custom-designed implants are used for surgery.",{"count":46,"type":20},100,"This study is part of the clinical evaluation of SEBBIN silicone gel-filled testicular implants, included in the technical file of the device. The aim of the study is to gather additional data about the safety and effectiveness of the device.",[24,25],{"date":29,"type":30},{"date":51,"type":30},"2021-03-16",{"date":53,"type":20},"2035-09",{"name":36,"class":37},""]