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- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07746050
Value of Biomarkers of Brain Injury for Predicting Psycho-cognitive Sequelae Secondary to Sepsis: a Prospective Multicenter Study (SEPSYM)
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Sepsis is a major cause of admission to intensive care units and is responsible for approximately 11 million deaths worldwide each year. It may be complicated by an acute brain dysfunction known as sepsis-associated encephalopathy (SAE), which affects about 50% of patients and typically manifests as delirium or coma. The diagnosis of SAE is primarily clinical, with EEG and brain MRI providing supportive information. Risk factors for SAE are mainly related to patient characteristics, including advanced age, chronic kidney disease, and pre-existing neurodegenerative or cognitive disorders. The pathophysiology of SAE involves three major mechanisms: neuroinflammation, endothelial dysfunction with blood-brain barrier disruption, and mitochondrial dysfunction leading to neuronal injury. These mechanisms likely explain both acute neurological symptoms and long-term psycho-cognitive sequelae. Following sepsis, 30-60% of patients develop psychiatric disorders and cognitive impairments comparable to those observed after moderate traumatic brain injury or early Alzheimer's disease. These sequelae are part of post-intensive care syndrome (PICS), supporting the need for structured post-ICU follow-up. However, the optimal target population and organization of such follow-up remain unclear, as some studies have reported reduced quality of life in patients receiving long-term follow-up. Identifying early biomarkers predictive of psycho-cognitive outcomes is therefore crucial, as current data on neuronal and glial biomarkers remain limited. Such biomarkers could improve prognostication, guide cognitive rehabilitation and psychological support, and contribute to the development of future neuroprotective strategies.
Primary objective:
To evaluate the value of biomarkers of brain injury for predicting cognitive impairment (memory impairment assessed by a MoCA score < 26/30) at 3 months.
Secondary objectives:
- To evaluate the value of brain injury biomarkers for predicting delirium in the ICU, including hypoactive, hyperactive, and mixed phenotypes
- To assess the association between brain injury biomarkers and the duration of delirium in the ICU
- To evaluate the value of brain injury biomarkers for predicting psychological sequelae (anxiety, post-traumatic stress disorder, and depression) at 3 months
- To evaluate the value of brain injury biomarkers for predicting functional neurological outcomes using the Glasgow Outcome Scale-Extended at ICU discharge and at 3 months
- To assess the association between brain injury biomarkers and Post-Intensive Care Syndrome (PICS)
- To assess the association between brain injury biomarkers and EEG abnormalities in the ICU
- To assess the association between brain injury biomarkers and MRI abnormalities at 3 months
Tipo de estudio
Inscripción (Estimado)
Fase
- No aplica
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Adèle BELLINO
- Número de teléfono: +33 01 71 76 07 57
- Correo electrónico: adele.bellino@aphp.fr
Copia de seguridad de contactos de estudio
- Nombre: Sarah BENGHANEM, Dr
- Número de teléfono: +33 01 58 41 25 25
- Correo electrónico: sarah.benghanem@aphp.fr
Ubicaciones de estudio
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Île-de-France Region
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Paris, Île-de-France Region, Francia, 75014
- Hôpital Cochin - APHP Centre
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Contacto:
- Sarah BENGHANEM, Dr
- Número de teléfono: +33 01 58 41 25 25
- Correo electrónico: sarah.benghanem@aphp.fr
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Adults aged 18-80 years.
- Admission to a medical or mixed ICU.
- Sepsis or septic shock according to Sepsis-3 criteria.
- ICU admission for less than 24 hours.
- Need for invasive or non-invasive mechanical ventilation and/or vasopressor support.
- Informed consent obtained from the patient or legal representative.
Exclusion Criteria:
- Moribund patients.
- Age >80 years.
- Patients under legal guardianship.
- History of schizophrenia or bipolar disorder.
- Pregnancy.
- No health insurance coverage.
- Previous inclusion in the study.
- Refusal to participate.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Diagnóstico
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Cognitive function impairment assessed by the Montreal Cognitive Assessment (MoCA) score at 3 months
Periodo de tiempo: 3 months
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Montreal Cognitive Assessment (MoCA) ranges from 0 to 30 points, with higher scores indicating better cognitive performance.
Cognitive impairment will be defined as a MoCA score <26/30.
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3 months
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Coma- and/or delirium-free days
Periodo de tiempo: Day 10 after inclusion
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Day 10 after inclusion
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Duration of delirium in the intensive care unit (ICU)
Periodo de tiempo: 3 months
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3 months
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Type of ICU delirium: hypoactive, hyperactive, or mixed
Periodo de tiempo: 3 months
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3 months
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Psychiatric disorders (anxiety, depression : ( 0 =min; 21 =max) , or PTSD)
Periodo de tiempo: 3 months
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3 months
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Glasgow Outcome Scale-Extended (GOSE)
Periodo de tiempo: 3 months
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3 months
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Delirium duration
Periodo de tiempo: 3 months
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Number of ICU days with delirium assessed using the Confusion Assessment Method for the ICU (CAM-ICU).
Delirium duration will be reported as the cumulative number of ICU days with at least one positive CAM-ICU assessment.
Higher values indicate longer delirium duration.
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3 months
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Delirium phenotype
Periodo de tiempo: 3 months
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ICU delirium phenotype classified as hypoactive, hyperactive or mixed according to CAM-ICU and RASS assessments.
Results will be reported as the proportion of patients in each category.
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3 months
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Psychiatric outcomes
Periodo de tiempo: 3 months
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Symptoms of anxiety and depression assessed using the Hospital Anxiety and Depression Scale (HADS; higher scores indicate greater symptom severity).
PTSD assessed using the PTSD Checklist (PCL-5).
Results will be reported as continuous scores and proportions of patients above validated thresholds
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3 months
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Functional outcome
Periodo de tiempo: 3 months
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Functional neurological outcome assessed using the Glasgow Outcome Scale-Extended (GOSE; range 1-8, higher scores indicate better functional recovery).
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3 months
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PICS : Post-Intensive Care Syndrome (PICS)
Periodo de tiempo: 3 months
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PICS is defined by the presence of cognitive impairment, psychiatric symptoms and/or physical disability at 3 months.
Results will be reported as the proportion of patients fulfilling at least one PICS domain.
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3 months
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Neurological, psychiatric, or rehabilitation follow-up proposed to the patient
Periodo de tiempo: 3 months
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Referral for specialized follow-up after ICU discharge.
This outcome will be reported as the proportion of patients referred to neurological consultation, psychiatric consultation, cognitive rehabilitation, physical rehabilitation and/or a multidisciplinary post-ICU clinic.
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3 months
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Sarah BENGHANEM, Dr, Assistance Publique - Hôpitaux de Paris
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
- Manifestaciones neurológicas
- Enfermedades del Sistema Nervioso
- Desordenes mentales
- Procesos Patológicos
- Infecciones
- Confusión
- Manifestaciones neuroconductuales
- Trastornos neurocognitivos
- Síndrome de Respuesta Inflamatoria Sistémica
- Inflamación
- Choque
- Condiciones Patológicas, Signos y Síntomas
- Signos y síntomas
- Delirio
- Septicemia
- Choque séptico
- Síndrome de cuidados postintensivos
Otros números de identificación del estudio
- APHP251947
- IDRCB (Otro identificador: 2025-A02589-40)
Plan de datos de participantes individuales (IPD)
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Información sobre medicamentos y dispositivos, documentos del estudio
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