[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Centre Hospitalier de Gonesse\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":169},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,7,0,[8,40,65,85,111,131,150],{"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":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":28,"lastUpdatePostDateStruct":29,"startDateStruct":32,"completionDateStruct":34,"leadSponsor":36,"locationsCount":39},"100606206","high-risk-of-death-or-disability-in-brain-hemorrhage-role-of-spot-sign-and-secondary-markers-100606206",false,"NCT07172542","High Risk of Death or Disability in Brain Hemorrhage: Role of Spot Sign and Secondary Markers","Inclusion Criteria:\n\n* Spontaneous intracerebral hemorrhage confirmed by contrast-enhanced CT scan.\n* Follow-up CT scan performed within 24 to 48 hours.\n\nNon-inclusion Criteria :\n\n* Absence of initial contrast-enhanced CT or follow-up CT.\n* Hematoma due to trauma, epidural hematoma (EDH), subdural hematoma (SDH), or subarachnoid hemorrhage (SAH).\n\nExclusion Criteria:\n\n* Patient deceased before the initial contrast-enhanced CT.\n* Major missing clinical data.","ALL","18 Years",{"count":18,"type":19},50,"ESTIMATED","OBSERVATIONAL","This study looks at patients with brain hemorrhage to see if a special sign on brain scans, called the \"Spot Sign,\" combined with other scan features, can predict a higher risk of death or disability. By comparing patient outcomes with existing prediction scores, the study aims to understand whether these scan markers provide extra value in identifying patients at higher risk.",[23,24,25,26],"Intracerebral Hemorrhage","Cerebral Hemorrhage","Stroke","Brain Injuries","NOT_YET_RECRUITING","2025-09-08",{"date":30,"type":31},"2025-09-15","ACTUAL",{"date":33,"type":19},"2025-10-15",{"date":35,"type":19},"2026-05-15",{"name":37,"class":38},"Centre Hospitalier de Gonesse","OTHER",1,{"id":41,"slug":42,"hasResults":11,"nctId":43,"briefTitle":44,"officialTitle":44,"acronym":4,"eligibilityCriteria":45,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":46,"targetDuration":4,"studyType":20,"phases":4,"briefSummary":48,"conditions":49,"keywords":4,"overallStatus":56,"whyStopped":4,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":64,"locationsCount":39},"100602389","eligibility-of-patients-referred-to-emergency-departments-by-their-general-practitioners-for-care-in-walk-in-clinics-a-single-center-study-in-le-de-france-100602389","NCT07122869","Eligibility of Patients Referred to Emergency Departments by Their General Practitioners for Care in Walk-in Clinics: A Single-Center Study in Île-de-France","Inclusion Criteria:\n\n* Age 18 years or older\n* Patient referred to the emergency department (ED) with a letter from a general practitioner (GP)\n* ED visit during the study hours (Monday to Friday, 9 a.m. to 8 p.m.)\n* Consultation in the selected adult emergency service\n* Medical or traumatic reason justifying the ED visit\n* Patient stable at arrival and during ED care\n\nExclusion Criteria:\n\n* Patients under 18 years old (pediatric cases excluded)\n* No referral letter or proof of GP referral\n* ED visit outside study hours (weekends, nights)\n* Patients requiring intensive hospital care defined by:\n* Intravenous treatments (e.g., antibiotics, fluids)\n* Heavy imaging exams (CT scan, MRI) during the visit\n* Diagnoses with immediate life- or function-threatening conditions (e.g., myocardial infarction, stroke, severe infection)\n* Hospitalization decided during or after ED visit\n* Clinical instability at or during ED visit (abnormal vital signs, respiratory distress, etc.)\n* Patients referred for non-medical reasons (social issues, lack of medical follow-up)",{"count":47,"type":19},80,"This study aims to find out how many patients sent to the emergency department by their general practitioner could instead be treated in a walk-in clinic. Walk-in clinics provide quick, basic medical care without an appointment and can perform simple tests like blood work and X-rays. By identifying patients who don't need full hospital emergency care, this study hopes to improve patient flow and reduce overcrowding in emergency rooms in the Île-de-France region.",[50,51,52,53,54,55],"Emergency Service, Hospital","Primary Health Care","General Practitioners","Walk-In Clinics","Patient Admission","Health Services Accessibility","RECRUITING","2025-08-08",{"date":59,"type":31},"2025-08-14",{"date":61,"type":31},"2025-07-28",{"date":63,"type":19},"2025-08-30",{"name":37,"class":38},{"id":66,"slug":67,"hasResults":11,"nctId":68,"briefTitle":69,"officialTitle":69,"acronym":4,"eligibilityCriteria":70,"healthyVolunteers":11,"sex":15,"minAge":4,"maxAge":4,"enrollmentInfo":71,"targetDuration":4,"studyType":20,"phases":4,"briefSummary":73,"conditions":74,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":80,"startDateStruct":81,"completionDateStruct":82,"leadSponsor":84,"locationsCount":39},"100602388","predictive-factors-for-initial-mmse-score-and-rapid-decline-in-alzheimers-disease-patients-100602388","NCT07122856","Predictive Factors for Initial MMSE Score and Rapid Decline in Alzheimer's Disease Patients","Inclusion Criteria:\n\n* Confirmed diagnosis of Alzheimer's disease according to NIAA 2018 or IWG 2021 criteria\n* At least two MMSE evaluations spaced 12 months apart\n* Follow-up at the Memory Clinic of CH Gonesse\n\nExclusion Criteria:\n\n* Presence of other neurodegenerative diseases (e.g., Frontotemporal Dementia, Multiple System Atrophy, Vascular Dementia, LATE)\n* Patient has moved out of the study area (outside the CH Gonesse territory)",{"count":72,"type":19},100,"This study looks at people with Alzheimer's disease to find out which factors are linked to their initial score on the Mini-Mental State Examination (MMSE) and which factors may predict a fast decline in their score over 12 months. Researchers will review medical records from patients seen at the Memory Clinic of Gonesse Hospital and analyze information such as age, education, medical history, nutrition, mood, and caregiver burden. The goal is to better understand what influences early cognitive performance and how quickly it changes, to help improve patient care and planning.",[75,76,77,78,79],"Alzheimer Disease","Mini-Mental State Examination","Cognitive Dysfunction","Neuropsychological Tests","Caregivers",{"date":59,"type":31},{"date":30,"type":19},{"date":83,"type":19},"2026-03-15",{"name":37,"class":38},{"id":86,"slug":87,"hasResults":11,"nctId":88,"briefTitle":89,"officialTitle":90,"acronym":4,"eligibilityCriteria":91,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":92,"targetDuration":4,"studyType":20,"phases":4,"briefSummary":94,"conditions":95,"keywords":4,"overallStatus":56,"whyStopped":4,"lastUpdateSubmitDate":103,"lastUpdatePostDateStruct":104,"startDateStruct":106,"completionDateStruct":108,"leadSponsor":110,"locationsCount":39},"100598281","prognostic-value-of-isolated-and-combined-score-aspects-in-acute-ischemic-stroke-100598281","NCT07069452","Prognostic Value of Isolated and Combined Score Aspects in Acute Ischemic Stroke","TARGET-ASPECT (Prognostic Value of Isolated and Combined Score Aspects in Acute Ischemic Stroke)","Inclusion Criteria :\n\n* Patients aged 18 years or older\n* Confirmed acute ischemic stroke on imaging\n* Treated with both thrombolysis and thrombectomy\n* Clinical follow-up data available at 90 days (mRS score)\n\nExclusion Criteria :\n\n* Primary hemorrhagic stroke\n* Early death or loss to follow-up without evaluation\n* Poor-quality imaging that cannot be analyzed",{"count":93,"type":19},152,"This study, called TARGET-ASPECT, looks at patients who had a type of stroke called acute ischemic stroke and were treated with clot-busting medicine and a procedure to remove the clot. Even with these treatments, about half of patients don't fully recover. The study aims to see if certain brain imaging scores, especially when combined, can better predict how well patients will recover 90 days after their stroke and if their blood vessels reopen successfully. The study will include 152 patients and last about 9 months. The goal is to find easy and reliable tools that doctors can use to make better treatment decisions.",[96,97,98,99,100,101,102],"Stroke, Ischemic","Thrombectomy","Thrombolytic Therapy","Brain Ischemia","Prognosis","Magnetic Resonance Imaging","Outcome Assessment (Health Care)","2025-07-15",{"date":105,"type":31},"2025-07-16",{"date":107,"type":31},"2025-04-15",{"date":109,"type":19},"2026-01-15",{"name":37,"class":38},{"id":112,"slug":113,"hasResults":11,"nctId":114,"briefTitle":115,"officialTitle":115,"acronym":4,"eligibilityCriteria":116,"healthyVolunteers":11,"sex":15,"minAge":4,"maxAge":4,"enrollmentInfo":117,"targetDuration":4,"studyType":20,"phases":4,"briefSummary":119,"conditions":120,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":124,"lastUpdatePostDateStruct":125,"startDateStruct":127,"completionDateStruct":129,"leadSponsor":130,"locationsCount":39},"100597882","assessment-of-interprofessional-competencies-of-healthcare-professionals-before-and-after-healthcare-simulation-sessions-100597882","NCT07064265","Assessment of Interprofessional Competencies of Healthcare Professionals Before and After Healthcare Simulation Sessions","Inclusion Criteria:\n\n* Medical students (interns and externs)\n* Paramedical students (nursing students, nurse assistants, nurse managers)\n* Healthcare professionals from Gonesse Hospital\n\nExclusion Criteria:\n\n* Administrative staff\n* Participants who have already taken part in previous simulation sessions",{"count":118,"type":19},200,"The aim of our study is to assess the interprofessional competencies of healthcare learners before and one month after interprofessional simulation sessions, and to demonstrate their impact on the work of healthcare professionals as part of their continuing education in a hospital setting.\n\nInitially, we will distribute a self-assessment questionnaire to all learners before the simulation sessions and again one month after the sessions.\n\nHospital-based healthcare professionals register for the simulation training through the continuing education department of Gonesse Hospital.\n\nPhysicians and medical students register through the training's designated physician.\n\nParamedical students register through the training's designated nurse manager.\n\nWe conduct two simulation training sessions per month on the topic of \"Adult Life-Threatening Emergencies: Cardiac Arrest.\"\n\nEach session is composed of an interprofessional group.\n\nBefore the start of the session, the questionnaire is distributed to all participants.\n\nLearners are asked to indicate only their profession and the date on the questionnaire.\n\nEach questionnaire is assigned a number in the order of collection to ensure anonymity.\n\nOne month later, we resend the same questionnaire by email to the participants.\n\nThis is a self-assessment questionnaire developed in Canada and scientifically validated, used to evaluate interprofessional collaboration competencies (Survey for the Achievement of Interprofessional Collaborative Competencies: SACCI).\n\nIn a second phase, we will compare the results of the self-assessment questionnaires completed before and one month after the simulation sessions, using statistical analysis via Excel spreadsheet.",[121,122,123],"Health Personnel","Interprofessional Relations","CONTINUING MEDICAL EDUCATION","2025-07-10",{"date":126,"type":31},"2025-07-14",{"date":128,"type":19},"2025-08-15",{"date":83,"type":19},{"name":37,"class":38},{"id":132,"slug":133,"hasResults":11,"nctId":134,"briefTitle":135,"officialTitle":135,"acronym":4,"eligibilityCriteria":136,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":137,"targetDuration":4,"studyType":20,"phases":4,"briefSummary":139,"conditions":140,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":143,"lastUpdatePostDateStruct":144,"startDateStruct":146,"completionDateStruct":147,"leadSponsor":149,"locationsCount":39},"100595252","screening-for-cognitive-disorders-in-multiple-sclerosis-100595252","NCT07030036","Screening for Cognitive Disorders in Multiple Sclerosis","Inclusion Criteria:\n\n* Patients aged 18 years or older\n* Diagnosed with multiple sclerosis (MS) for at least 6 months according to the 2017 McDonald criteria (SFSEP)\n* Receiving disease-modifying treatment and followed in the neurology day hospital of CH Gonesse\n\nExclusion Criteria:\n\n\\- Under 18 years old",{"count":138,"type":19},60,"This study aims to identify cognitive problems in adults with multiple sclerosis (MS). MS can affect memory, thinking speed, and spatial skills, which may impact daily life and work. We will use simple and proven tests to check for these difficulties and see how they affect quality of life. The study will include about 60 patients followed at the neurology day hospital.",[141,77,78,142],"Multiple Sclerosis","Quality of Life","2025-06-12",{"date":145,"type":31},"2025-06-19",{"date":103,"type":19},{"date":148,"type":19},"2025-11-15",{"name":37,"class":38},{"id":151,"slug":152,"hasResults":11,"nctId":153,"briefTitle":154,"officialTitle":154,"acronym":4,"eligibilityCriteria":155,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":156,"targetDuration":4,"studyType":20,"phases":4,"briefSummary":158,"conditions":159,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":162,"lastUpdatePostDateStruct":163,"startDateStruct":165,"completionDateStruct":167,"leadSponsor":168,"locationsCount":39},"100592484","feasibility-study-of-a-relapse-investigation-questionnaire-administered-by-an-ms-care-coordinator-nurse-in-patients-with-multiple-sclerosis-100592484","NCT06994026","Feasibility Study of a Relapse Investigation Questionnaire Administered by an MS Care Coordinator Nurse in Patients With Multiple Sclerosis","Inclusion Criteria:\n\n* Patients followed by Dr. Manchon for Relapsing-Remitting Multiple Sclerosis or active Secondary Progressive Multiple Sclerosis\n* Adult patients (aged 18 or older)\n* Patients who have provided informed consent for participation in the local task-sharing protocol\n\nExclusion Criteria:\n\n* Pregnant women\n* Minors (under 18 years old)\n* Patients with known renal failure\n* Patients who have not provided or are unable to provide consent for the local task-sharing protocol",{"count":157,"type":19},10,"This study aims to evaluate a questionnaire used by a specialized nurse to help manage relapses in people with multiple sclerosis (MS). The questionnaire is completed during a phone call when the patient reports new or worsening symptoms. It helps the nurse decide whether further tests or treatments are needed, based on a protocol developed with a neurologist. The goal is to improve how quickly and effectively patients receive care during a relapse. The study will include 10 adult patients with active forms of MS over a two-month period.",[141,160,161],"Disease Management","Feasibility Studies","2025-05-20",{"date":164,"type":31},"2025-05-29",{"date":166,"type":19},"2025-06-15",{"date":128,"type":19},{"name":37,"class":38},""]