[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Ceribell Inc.\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":89},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,41,65],{"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":4,"studyType":20,"phases":4,"briefSummary":21,"conditions":22,"keywords":24,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100630251","eeg-abnormalities-in-adult-icu-patients-with-high-risk-of-delirium-100630251",false,"NCT07485244","EEG Abnormalities in Adult ICU Patients With High Risk of Delirium","Inclusion Criteria:\n\n* Adult patient ≥18 years old\n* Requiring admission to a medical, surgical and\u002For cardiovascular ICU for an expected duration ≥ 24 hours\n* Receiving treatment for shock (e.g., with vasopressors, intra-aortic balloon pump, or Extracorporeal Membrane Oxygenation therapy) and\u002For respiratory failure \\[e.g., on mechanical ventilation or non-invasive positive pressure ventilation (NIPPV)\\].\n\nExclusion Criteria:\n\n* Any structural abnormality or head condition, including the presence of a device, that would prevent the use of the Ceribell EEG system for the entire anticipated EEG monitoring period. Examples include: Craniectomy with a missing bone flap in a region where Ceribell EEG electrodes would be placed.\n* Anticipated use of continuous EEG for a purpose other than delirium detection during the entire expected monitoring period.\n* Patients who have been on mechanical ventilation for \\>72 hours within the current hospitalization or who are on long-term ventilator support prior to the injury that resulted in the current hospitalization.\n* Expected death within 12 hours of enrollment or lack of commitment to treatment by family or the medical team (e.g., likely to withdraw life support measures within 12 hours of enrollment).\n* Acute or chronic neurologic deficit precluding CAM-ICU assessments\n* Inability to understand English\n* Bilateral Deafness\n* Blindness that will preclude delirium evaluation\n* Current enrollment in a study that does not allow co-enrollment\n* Inability to obtain informed consent\n* Attending physician refusal\n* Patient and\u002For surrogate refusal\n* Patient unable to consent and no surrogate available\n* Prisoners","ALL","18 Years",{"count":18,"type":19},100,"ESTIMATED","OBSERVATIONAL","The purpose of this study is to assess the prevalence of EEG abnormalities on Ceribell POC EEG in adult medical, surgical, and cardiovascular ICU patients with high risk of delirium",[23],"Delirium in the Intensive Care Unit",[25,26,27,28],"Ceribell","Electroencephalogram (EEG)","Delirium monitoring","Delirium","RECRUITING","2026-04-16",{"date":32,"type":33},"2026-04-21","ACTUAL",{"date":30,"type":33},{"date":36,"type":19},"2027-09-30",{"name":38,"class":39},"Ceribell Inc.","INDUSTRY",1,{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":45,"acronym":46,"eligibilityCriteria":47,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":48,"targetDuration":4,"studyType":49,"phases":50,"briefSummary":52,"conditions":53,"keywords":54,"overallStatus":56,"whyStopped":4,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":64,"locationsCount":40},"100627498","ceribell-delirium-monitor-outcomes-pilot-study-100627498","NCT07449416","Ceribell Delirium Monitor Outcomes Pilot Study","DOM","Inclusion Criteria:\n\n* Age is 18 years or older\n* Admitted to the ICU for an expected duration ≥ 24 hours from enrollment\n* Have at least one of the following conditions:\n\nAcute Sepsis or Septic Shock Admitted to the ICU following elective cardiothoracic surgery Acute respiratory failure requiring non-invasive ventilation or high-flow nasal cannula (HFNC) oxygenation Shock requiring vasopressor therapy Mechanically ventilated - Current RASS ≥ -3 and not expected to require deep sedation (RASS \\\u003C -3) during the ICU stay\n\nExclusion Criteria:\n\n\\- Any structural abnormality or head condition, including the presence of a device, that would prevent the use of the Ceribell EEG system for the entire anticipated EEG monitoring period. Examples include: Craniectomy with a missing bone flap in a region where Ceribell EEG electrodes would be placed.\n\nAnticipated use of continuous EEG for a purpose other than delirium detection during the entire expected monitoring period.\n\n* Baseline neurological dysfunction (Glasgow Coma Scale \\\u003C 10) and pre-existing brain injuries such as stroke with known deficits, severe TBI\n* History of moderate-severe dementia (IQCODE ≥ 3.5)\n* APACHE II score \\> 30, or SOFA \\> 9 at enrollment",{"count":18,"type":19},"INTERVENTIONAL",[51],"NA","This pilot study is designed as a pre- and post-delirium monitor cohort study, with a prospective intervention cohort and a retrospective control cohort.",[23],[28,55,25,26],"Delirium Monitoring","NOT_YET_RECRUITING","2026-02-27",{"date":59,"type":33},"2026-03-04",{"date":61,"type":19},"2026-03-15",{"date":63,"type":19},"2026-12",{"name":38,"class":39},{"id":66,"slug":67,"hasResults":11,"nctId":68,"briefTitle":69,"officialTitle":69,"acronym":4,"eligibilityCriteria":70,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":71,"targetDuration":73,"studyType":20,"phases":4,"briefSummary":74,"conditions":75,"keywords":76,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":80,"lastUpdatePostDateStruct":81,"startDateStruct":83,"completionDateStruct":85,"leadSponsor":87,"locationsCount":88},"100436405","ceribell-delirium-data-collection-study-100436405","NCT04962815","Ceribell Delirium Data Collection Study","Inclusion Criteria: All must be present\n\n* Age is 18 years or older\n* Admitted to the Intensive Care Unit (ICU)\n* Subject must be fluent in the language in which the delirium assessment is performed\n\nExclusion Criteria: All must be absent\n\n\\- Any condition that prevents use of the Ceribell EEG system on the subject for the entire anticipated EEG monitoring period. Examples may include: Craniectomy with missing bone flap in an area where Ceribell EEG electrodes are placed. Expected use of continuous clinical EEG for the entire anticipated monitoring period.",{"count":72,"type":19},200,"6 Days","This study is designed as a prospective, non-randomized, observational clinical study. The study will collect clinical and rrEEG (Ceribell EEG) data when monitoring subjects for delirium subtypes. EEG and clinical data will be collected for the development of future software algorithms to assess the presence and severity of delirium.",[28],[77,78,79],"delirium","EEG","Electroencephalogram","2025-07-22",{"date":82,"type":33},"2025-07-25",{"date":84,"type":33},"2021-11-10",{"date":86,"type":19},"2026-04-01",{"name":38,"class":39},7,""]