[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100444798":3},{"organization":4,"armGroups":7,"interventions":22,"overallOfficials":28,"centralContacts":32,"locations":37,"responsibleParty":55,"collaborators":10,"id":58,"slug":59,"hasResults":60,"nctId":61,"briefTitle":62,"officialTitle":63,"acronym":10,"eligibilityCriteria":64,"healthyVolunteers":60,"sex":65,"minAge":66,"maxAge":10,"enrollmentInfo":67,"targetDuration":70,"studyType":71,"phases":10,"briefSummary":72,"conditions":73,"keywords":10,"overallStatus":40,"whyStopped":10,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":81,"completionDateStruct":83,"leadSponsor":85,"locationsCount":86},{"fullName":5,"class":6},"University of Campania Luigi Vanvitelli","OTHER",[8,14,18],{"label":9,"type":10,"description":11,"interventionNames":12},"Patients with PM",null,"All patients underwent PM implantation",[13],"Device: Device implantation",{"label":15,"type":10,"description":16,"interventionNames":17},"Patients with ICD","All patients undeerwent ICD implantation",[13],{"label":19,"type":10,"description":20,"interventionNames":21},"Patients with ILR","All patients underwent ILR implantation",[13],[23],{"type":24,"name":25,"description":26,"armGroupLabels":27,"otherNames":10},"DEVICE","Device implantation","Implantation of single chamber, dual chambers or triple chambers PM\u002FICD",[15,19,9],[29],{"name":30,"affiliation":5,"role":31},"Vincenzo Russo, MD PhD","STUDY_CHAIR",[33],{"name":30,"role":34,"phone":35,"phoneExt":10,"email":36},"CONTACT","+390817062355","vincenzo.russo@unicampania.it",[38],{"facility":39,"status":40,"city":41,"state":42,"zip":43,"country":44,"countryCode":45,"cosmosGeoPoint":46,"geoPoint":51,"contacts":52},"Vincenzo Russo","RECRUITING","Naples","Napoli","80136","Italy","IT",{"type":47,"coordinates":48},"Point",[49,50],14.26811,40.85216,{"lat":50,"lon":49},[53],{"name":30,"role":34,"phone":10,"phoneExt":10,"email":54},"v.p.russo@libero.it",{"type":56,"investigatorFullName":39,"investigatorTitle":57,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"PRINCIPAL_INVESTIGATOR","Principal Investigator","100444798","monaldi-hospital-rhythm-registry-100444798",false,"NCT05072119","Monaldi Hospital Rhythm Registry","Registry of Patients Underwent Cardiac Implanted Electronic Device Implantation at Monaldi Hospital","Inclusion Criteria:\n\n* All consecutive patients underwent PM\u002FICD\u002FILR implantation\n* Patient is willing and able to sign an authorization to use and disclose health information or an Informed Consent\n* Patient must be able to attend all required follow-up visits at the study center for at least 12 months\n\nExclusion Criteria:\n\n* No informed consent\n* Patient is participating in another clinical study that may have an impact on the study endpoint\n\nExclusion Criteria:\n\n* No informed consent","ALL","14 Years",{"count":68,"type":69},5000,"ESTIMATED","20 Years","OBSERVATIONAL","The study is a prospective registry. Consecutive patients with indications of implant \u002F replacement or upgrade of pacemaker (PM), implantable cardioverter defibrillator (ICD), Implanted loop recorder (ILR) will be enrolled.\n\nThe primary objective of the study is to describe the clinical events during a long-term follow-up of non-selected population of patients implanted with an PM, ICD or ILR.",[74,75,76],"Pacemaker","ICD","Implanted Loop Recorder","2021-10-08",{"date":79,"type":80},"2021-10-15","ACTUAL",{"date":82,"type":80},"2015-01-07",{"date":84,"type":69},"2050-01",{"name":5,"class":6},1]