[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100504107":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":33,"centralContacts":33,"locations":34,"responsibleParty":57,"collaborators":60,"id":73,"slug":74,"hasResults":75,"nctId":76,"briefTitle":77,"officialTitle":78,"acronym":33,"eligibilityCriteria":79,"healthyVolunteers":80,"sex":81,"minAge":82,"maxAge":33,"enrollmentInfo":83,"targetDuration":33,"studyType":86,"phases":87,"briefSummary":89,"conditions":90,"keywords":93,"overallStatus":96,"whyStopped":33,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":101,"completionDateStruct":103,"leadSponsor":105,"locationsCount":106},{"fullName":5,"class":6},"Università degli Studi di Sassari","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Ks dental implant","EXPERIMENTAL","Innovative dental implant with lasting, internal conical connection of 15° and strengthened implant walls.",[13],"Device: Implant placement ks",{"label":15,"type":16,"description":17,"interventionNames":18},"TSIII dental implant","ACTIVE_COMPARATOR","Standard dental implant with internal conical connection of 11°.",[19],"Device: Implant placement TS III",[21,28],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"DEVICE","Implant placement TS III","Implant placement in subjects who have lost at least two teeth and need a prosthetic implant rehabilitation with TSIII Implant. . After osseointegration, dental implants will receive definitive prosthesis.",[15],[27],"Dental prosthesis delivery",{"type":22,"name":29,"description":30,"armGroupLabels":31,"otherNames":32},"Implant placement ks","Implant placement in subjects who have lost at least two teeth and need a prosthetic implant rehabilitation with KS Implant. After osseointegration, dental implants will receive definitive prosthesis.",[9],[27],null,[35],{"facility":36,"status":33,"city":37,"state":33,"zip":38,"country":39,"countryCode":40,"cosmosGeoPoint":41,"geoPoint":46,"contacts":47},"Marco Tallarico","Sassari","07100","Italy","IT",{"type":42,"coordinates":43},"Point",[44,45],8.55552,40.72586,{"lat":45,"lon":44},[48,53],{"name":49,"role":50,"phone":51,"phoneExt":33,"email":52},"Dario Melodia, Dr","CONTACT","3331226618","dariomld1@gmail.com",{"name":54,"role":50,"phone":55,"phoneExt":33,"email":56},"Marco Tallarico, Prof","3280758769","me@studiomarcotallarico.it",{"type":58,"investigatorFullName":36,"investigatorTitle":59,"investigatorAffiliation":5,"oldNameTitle":33,"oldOrganization":33},"PRINCIPAL_INVESTIGATOR","Assistant professor",[61,64,66,69,71],{"name":62,"class":63},"Melodia, Dario, M.D.","INDIV",{"name":65,"class":63},"Pisano, Milena, M.D.",{"name":67,"class":68},"Dr. Aurea Lumbau","UNKNOWN",{"name":70,"class":63},"Meloni, Silvio Mario, M.D.",{"name":72,"class":63},"Baldoni, Edoardo, M.D.","100504107","comparison-ks-versus-ts-100504107",false,"NCT05843981","Comparison KS Versus TS","The Use of an Innovative, Thickened and Lasting Implant Comparing KS Versus TS Implants for Prosthetic Rehabilitations","Inclusion Criteria:\n\nAny partially edentulous patient with partial edentulism, requiring at least two dental implant-supported rehabilitations, being 18 years or older, and able to sign an informed consent. Implant sites must allow the placement of two implants of at least 4 (premolars) or 4.5 (molars) mm of diameter and 8.5 mm of length. Smokers will be included and categorized into: 1) non smokers; 2) moderate smokers (smoking up to 10 cigarettes\u002Fday); 3) heavy smokers (smoking more than 11 cigarettes\u002Fday). In case of post-extractive sites, they must have been healing for at least 3 months before being treated in the study. Implants can be adjacent.\n\nExclusion Criteria:\n\n* General contraindications to implant surgery.\n* Patients irradiated in the head and neck area.\n* Immunosuppressed or immunocompromised patients.\n* Patients treated or under treatment with intravenous amino-bisphosphonates.\n* Patients with untreated periodontitis.\n* Patients with poor oral hygiene and motivation.\n* Previous guided bone reconstruction at the intended implant sites.\n* Uncontrolled diabetes.\n* Pregnancy or nursing.\n* Substance abuser.\n* Psychiatric problems or unrealistic expectations.\n* Lack of opposite occluding dentition in the area intended for implant placement.\n* Patients with infection and or inflammation in the area intended for implant placement.\n* Patients participating in other studies, if the present protocol cannot be properly adhered to.\n* Patients referred only for implant placement and cannot be followed ant the treating centre.\n* Patients unable to be followed for 5 years.",true,"ALL","18 Years",{"count":84,"type":85},42,"ESTIMATED","INTERVENTIONAL",[88],"NA","To compare the clinical and radiographic outcomes of two different implant systems with different implant-abutment connection: Osstem TS III (control group) versus Osstem KS (study group).",[91,92],"Dental Implant","Dental Implant-Abutment Design",[92,94,95],"KS dental implant","Implant-abutment connection","NOT_YET_RECRUITING","2024-02-21",{"date":99,"type":100},"2024-02-23","ACTUAL",{"date":102,"type":85},"2024-03-01",{"date":104,"type":85},"2028-01-31",{"name":5,"class":6},1]