- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT02436616
microEEG for Neonatal Apnea, Bradycardia and Desaturation
Wireless Novel microEEG for Neonatal Apnea and Community Neurological Network
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Most preterm infants have episodes of apnea (cessation of breathing), bradycardia (low heart rate), and desaturations (low levels of oxygen in the blood) (ABD events). The resolution of ABD episodes depends to a large extent on the maturation of the central nervous system (CNS). The electroencephalogram (EEG) is a reliable and noninvasive tool for recording the electrical activity of the CNS. The relationship between ABD events and cerebral electrical activity has not been well investigated. The investigators seek to examine the relationship between EEG findings and the resolution of ABD events in the developing premature infant.
To investigate this relationship and obtain findings which are relevant to clinical care, a variety of obstacles need to be overcome. Among these obstacles is the high cost of standard EEG machines, inability of most standard machines to operate in electrically-noisy environments such as the NICU, and the absence of full-time coverage neurologists for prompt EEG interpretation. The investigators seek to determine the feasibility of obtaining an artifact-free EEG in the NICU with accurate detection of background rhythm abnormalities. The investigators will utilize an existing digital wireless telemetry unit, the "microEEG" for the NICU for this purpose. The microEEG device is specifically designed to overcome obstacles to standard EEG recording.
To address the shortage of trained pediatric neurophysiologists, the investigators will investigate the feasibility of a case management system for centralized EEG interpretation using off-site neurologists.
Finally, the investigators will examine the inter-rater reliability of EEG interpretation in the developing premature infant. This will allow the development of consensus guidelines for EEG interpretations.
Tipo de estudio
Inscripción (Anticipado)
Contactos y Ubicaciones
Ubicaciones de estudio
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New York
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Brooklyn, New York, Estados Unidos, 11203
- Reclutamiento
- State University of New York/Downstate Medical Center
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Contacto:
- Zachary Ibrahim, MD
- Número de teléfono: 718-613-8442
- Correo electrónico: zachary.Ibrahim@downstate.edu
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Contacto:
- Geetha Chari, MD
- Número de teléfono: 9177600714
- Correo electrónico: geetha.chari@downstate.edu
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Brooklyn, New York, Estados Unidos, 11212
- Reclutamiento
- Brookdale University Hospital and Medical Center,
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Contacto:
- Roger Kim, MD
- Número de teléfono: 917-836-3613
- Correo electrónico: rkim@brookdale.edu
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Método de muestreo
Población de estudio
Descripción
Inclusion Criteria:
- gestational age (GA) 24-32 weeks
postnatal ages 0-30 days. The patients will be recruited upon manifesting one of the following
- apneas (cessation of breathing > 10 seconds) x2 in a 12 hour span
- bradycardias (HR < 100/min) x2 in 12 hours
- oxygen desaturations (<80%) x 2 in 12 hours
- a single ABD event that does not resolve with stimulation or an increase in fractional oxygen delivery (FiO2).
Exclusion Criteria:
- major malformations
- The infant has exposed dermis on the scalp due to immaturity
Any scalp skin lesions such as pustules, large abrasions The patient will be Withdrawn if
- Informed consent is withdrawn
- adverse events (i.e..scalp lesions) develop
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
Cohortes e Intervenciones
Grupo / Cohorte |
Intervención / Tratamiento |
|---|---|
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EEG monitoring
All subjects enrolled in this observational study will undergo EEG monitoring using the microEEG device.
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microEEG is a miniature, wireless, and battery-powered EEG device used to obtain EEG recording in challenging environment. All infants have an initial EEG at study enrollment. Follow up microEEGs will be performed at approximately 2-4 week intervals, depending on the Corrected Gestational Age (CGA). If ABD events have not resolved at 34 weeks, an 8 hour recording will be performed prior to discharge or at 42 weeks CGA, whichever comes first. EEG will be assessed in 3 hour epochs. The EEG will be reviewed off line by two blinded neurologists and classified as normal or abnormal based on CGA and other findings. Follow up EEGs will be scored similarly, with emphasis on maturation. |
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Correlation between EEG background activity and resolution of Apnea, Bradycardia and Desaturation
Periodo de tiempo: Initial 8-9 hours EEG will be done upon study enrollment in the first 30 days of life.
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Primary outcome measure is to assess the background EEG activity in infants with ABD events and determine the relationship between abnormal initial EEG background activity and the resolution of ABD events at 34 weeks Corrected Gestational Age
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Initial 8-9 hours EEG will be done upon study enrollment in the first 30 days of life.
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Rate of seizure activity.
Periodo de tiempo: From study enrollement to resolution of ABD events or 42 weeks corrected gesational age, whichever, comes first.
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All EEG recordings will be assessed by a pediatric neurophysiologist for seizure activity using standard clinical criteria.
Based on their findings the rate of seizure will be determined.
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From study enrollement to resolution of ABD events or 42 weeks corrected gesational age, whichever, comes first.
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Feasibility of microEEG recording in the NICU
Periodo de tiempo: From study enrollment (first 30 days of life) to resolution of ABD events or 42 weeks gesational age (whichever comes first)
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Assess the ability of neonatal staff to utilize the microEEG to obtain EEG in the NICU.
This will be done by measuring the percentage of completed recordings that are interpretable by a pediatric neurophysiologist.
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From study enrollment (first 30 days of life) to resolution of ABD events or 42 weeks gesational age (whichever comes first)
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Interrater reliability of neonatal EEG interpretation
Periodo de tiempo: From study enrollment (first 30 days of life) to resolution of ABD events or 42 weeks gesational age (whichever comes first)
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Assess the inter-rater reliability of neonatal EEG interpretations using data obtained in the course of the study.
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From study enrollment (first 30 days of life) to resolution of ABD events or 42 weeks gesational age (whichever comes first)
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Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Zachary Ibrahim, MD, State University of New York - Downstate Medical Center
Publicaciones y enlaces útiles
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización primaria (Anticipado)
Finalización del estudio (Anticipado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
Actualizaciones de registros de estudio
Última actualización publicada (Estimar)
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
- Procesos Patológicos
- Enfermedades cardíacas
- Enfermedades cardiovasculares
- Enfermedades del Sistema Nervioso
- Enfermedades de las vías respiratorias
- Trastornos de la respiración
- Manifestaciones neurológicas
- Signos y Síntomas Respiratorios
- Arritmias Cardiacas
- Complicaciones del embarazo
- Complicaciones obstétricas del parto
- Trabajo de parto prematuro, obstétrico
- Apnea
- Nacimiento prematuro
- Bradicardia
- Convulsiones
Otros números de identificación del estudio
- 307016-7
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .
Ensayos clínicos sobre microEEG
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Bio-Signal Group Corp.National Institute of Neurological Disorders and Stroke (NINDS); State University... y otros colaboradoresTerminadoEstado mental alteradoEstados Unidos