[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100637592":3},{"organization":4,"armGroups":7,"interventions":8,"overallOfficials":7,"centralContacts":7,"locations":7,"responsibleParty":12,"collaborators":7,"id":14,"slug":7,"hasResults":15,"nctId":16,"briefTitle":17,"officialTitle":18,"acronym":7,"eligibilityCriteria":19,"healthyVolunteers":15,"sex":20,"minAge":21,"maxAge":7,"enrollmentInfo":22,"targetDuration":7,"studyType":25,"phases":7,"briefSummary":26,"conditions":27,"keywords":7,"overallStatus":29,"whyStopped":7,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":7},{"fullName":5,"class":6},"Xijing Hospital","OTHER",null,[9],{"type":6,"name":10,"description":11,"armGroupLabels":7,"otherNames":7},"Non-invasive cerebral Electrical Impedance Tomography (EIT) monitoring","Non-invasive real-time cerebral physiological monitoring performed by attaching standard scalp electrodes and collecting continuous cerebral bio-impedance signals via an Electrical Impedance Tomography (EIT) system. This monitoring is conducted synchronously with routine invasive intracranial pressure and arterial blood pressure monitoring in neurocritical care. It is purely an observational measurement procedure without any therapeutic intervention or modification to standard clinical treatment for participants, aiming to derive EIT-based parameters for evaluating cerebral blood flow autoregulation function.",{"type":13,"investigatorFullName":7,"investigatorTitle":7,"investigatorAffiliation":7,"oldNameTitle":7,"oldOrganization":7},"SPONSOR","100637592",false,"NCT07602114","Observational Study of Electrical Impedance Tomography for Non-Invasive Assessment of Cerebral Autoregulation in Neurocritical Patients","A Clinical Study of Non-Invasive Assessment of Cerebral Autoregulation Using Electrical Impedance Tomography","Inclusion Criteria:\n\n* Aged ≥18 years old\n* Diagnosed with acute intracerebral hemorrhage, subarachnoid hemorrhage or ischemic stroke, admitted to the Neurosurgical Intensive Care Unit\n* Receiving routine invasive monitoring of intracranial pressure (ICP) and mean arterial pressure (MAP)\n* Written informed consent obtained from the legally authorized representative\n\nExclusion Criteria:\n\n* Severe scalp damage, infection or skull defect affecting electrode placement\n* Craniotomy history with metal implants interfering with EIT signal acquisition Pregnancy\n* Terminal critical illness with estimated survival \\\u003C24 hours\n* Severe coagulation dysfunction or confirmed allergy to electrode materials\n* Unavailable for ≥2-hour continuous valid monitoring data collection","ALL","18 Years",{"count":23,"type":24},100,"ESTIMATED","OBSERVATIONAL","This is a single-center, prospective, observational, self-controlled clinical study conducted at the Neurosurgical Intensive Care Unit of Xijing Hospital, The First Affiliated Hospital of Air Force Military Medical University. The study aims to evaluate whether non-invasive Electrical Impedance Tomography (EIT) can reliably assess cerebral blood flow autoregulation in neurocritically ill participants, by comparing EIT-derived parameters with the current gold-standard invasive index PRx.\n\nCerebral blood flow autoregulation helps maintain stable brain perfusion in critically ill neurological patients. Impaired autoregulation raises the risk of secondary brain injury. The current standard evaluation requires invasive intracranial pressure monitoring, which carries risks of infection, bleeding, and tissue damage. EIT is a non-invasive, radiation-free bedside monitoring technique that uses scalp electrodes to measure real-time changes related to cerebral blood flow, with no additional harm to participants.\n\nAdult participants admitted to the neurosurgical intensive care unit who require routine invasive intracranial pressure monitoring will be enrolled, with informed consent provided by legal guardians. All participants receive standard clinical care as prescribed by current medical guidelines; no extra experimental treatments, drugs, or invasive procedures are applied for this study.\n\nDuring the study, invasive monitoring data and non-invasive EIT brain monitoring data will be collected simultaneously. Researchers will analyze the correlation and consistency between EIT-derived parameters and the gold-standard index.\n\nThis study has received ethical approval from the Medical Ethics Committee of The First Affiliated Hospital, Air Force Military Medical University. All participant information is anonymized to protect privacy, and adverse events will be recorded and reported in accordance with regulatory requirements. The results are expected to support a safe, non-invasive monitoring method for cerebral blood flow autoregulation in neurocritical care.",[28],"Homeostasis","NOT_YET_RECRUITING","2026-05-24",{"date":32,"type":33},"2026-05-28","ACTUAL",{"date":35,"type":24},"2026-05-30",{"date":37,"type":24},"2028-05-30",{"name":5,"class":6}]