- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT00971672
Incidence of Iron Deficiency Anemia in Toddlers
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
The purpose of this study is to analyze the frequency of Iron deficiency anemia in a group of 400 toddles from age 18 months to 36 months.
Two groups of children will be included, 200 children from Jewish origin and 200 from non Jewish origin, mostly Arabs.
A questionnaire that included demographic characteristics, nutrition and iron supplementation in the first year, growth status, and laboratory results will be filled for each patient.
The laboratory analysis will include complete blood count and serum ferritin analysis.
Children that were previously diagnosed suffering from iron deficiency, children suffering from chronic diseases or were born premature will not be included in the study.
Tipo de estudio
Inscripción (Actual)
Contactos y Ubicaciones
Ubicaciones de estudio
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Afula, Israel, 18101
- Pediatric Hematology Unit - Ha'Emek Medical Center
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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
The purpose of this study is to analyze the frequency of Iron deficiency anemia in a group of 400 toddles from age 18 months to 36 months.
Two groups of children will be included, 200 children from Jewish origin and 200 from non Jewish origin, mostly Arabs.
Children that were previously diagnosed suffering from iron deficiency, children suffering from chronic diseases or were born premature will not be included in the study.
Descripción
Inclusion Criteria:
- Healthy children that attend the pediatric community clinics.
Exclusion Criteria:
- Children that were previously diagnosed suffering from iron deficiency.
- Children suffering from chronic diseases or were born premature will not be included in the study.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
Cohortes e Intervenciones
Grupo / Cohorte |
Intervención / Tratamiento |
---|---|
Toddlers from Jewish origin
Toddlers from Jewish origin aged 18 to 36 months
|
A questionnaire that included demographic characteristics, nutrition and iron supplementation in the first year, growth status, and laboratory results will be filled for each patient. The laboratory analysis will include complete blood count and serum ferritin analysis. |
Toddlers from non Jewish origin
Toddlers aged 18 to 36 months belonging to non Jewish (Arab) population
|
A questionnaire that included demographic characteristics, nutrition and iron supplementation in the first year, growth status, and laboratory results will be filled for each patient. The laboratory analysis will include complete blood count and serum ferritin analysis. |
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Periodo de tiempo |
---|---|
Frequency of anemia (Hemoglobin below normal for age) and Iron deficiency (Low ferritin value)
Periodo de tiempo: One year
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One year
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Ariel Koren, MD, Pediatric Dpt B and Pediatric Hemaology Unit - Ha'Emek Medical Center - Afula - Israel
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización primaria (Actual)
Finalización del estudio (Actual)
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
Otros números de identificación del estudio
- 0024/09-EMC
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. .