Predicting Neurological Outcome Following Out of Hospital Cardiac Arrest (OHCA) by Quantitative Measurement of Serial Serum Biomarkers of Brain Injury.
Colección de datos
Recopilados desde hoy en adelante - ProspectivoHipoxia+14
+ Isquemia cerebral
+ Trastornos Cerebrovasculares
Cohorte
Seguimiento de la incidencia de una enfermedad para identificar factores de riesgo y comprender su progresión a lo largo del tiempo.Resumen
Fecha de inicio: 26 de mayo de 2017
Fecha en la que se inscribió al primer participante.This study focuses on individuals who experience a cardiac arrest outside of the hospital, a condition known as Out-of-Hospital Cardiac Arrest (OHCA). While some patients regain a heartbeat after aggressive treatment, many face poor outcomes, including low survival rates and potential neurological damage due to lack of oxygen to the brain. Currently, there's no quick, definitive test to predict the neurological outcome for these patients. This research aims to identify biomarkers, or substances in the blood, that could help predict such outcomes, potentially improving care and addressing current challenges in managing OHCA. The study involves a minimal risk procedure where blood samples are taken at various time points after the heartbeat is restored, specifically at 0-59 minutes, and then at 6, 12, 18, 24, 48, 72 hours, and on days 4, 5, and 6. The researchers will examine if the levels of certain biomarkers in these samples correlate with survival to hospital admission, survival to hospital discharge, and neurological function at discharge and after 6 months. The study also includes patients who come to the emergency department with chest pain but not cardiac arrest, to provide a comparative group.
Protocolo
Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.Se reclutarán 32 pacientes
Número total de participantes que el ensayo clínico espera reclutar.Cohorte
Elegibilidad
Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.Cualquier sexo
Sexo biológico de los participantes elegibles para inscribirse.A partir de 18 años
Rango de edades de los participantes que pueden unirse al estudio.Voluntarios sanos permitidos
Indica si personas sanas, sin la condición que se estudia, pueden participar.Condiciones
Patología
Criterios
Inclusion Criteria: \- \>18 years old Study cohort: * Non-traumatic out of hospital cardiac arrest * Control cohort: * Chest pain of non-cardiac etiology Exclusion Criteria: Both cohorts: * Females of child bearing age with positive pregnancy test * Neurodegenerative disease or other neurological disorder (dementia, Parkinson's disease, multiple sclerosis, seizure disorder, or brain tumours) * History of neurosurgery within the last 30 days Acute brain injury within the last 30 days (ischemic/ haemorrhagic stroke, traumatic brain injury) Subject is anemic OR donated blood within the last 8 weeks OR has a hematological disorder that requires transfusions Subject has history of liver failure OR renal failure Study cohort: Advanced directives against resuscitation Traumatic cardiac arrest In hospital cardiac arrest Failure to attain ROSC + visible signs of death (livor mortis, rigor mortis) Control cohort: EKG changes: New ST-elevation consistent with myocardial infarction NSTEMI Hemodynamically unstable
Plan de Estudio
Conoce todos los tratamientos administrados en este estudio, su descripción detallada y en qué consisten.Objetivos del Estudio
Objetivos Primarios
Objetivos Secundarios
Centros del Estudio
Estos son los hospitales, clínicas o centros de investigación donde se lleva a cabo el estudio. Puedes encontrar la ubicación más cercana a ti y su estado de reclutamiento.Este estudio tiene una ubicación