- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT01733849
A Study to Estimate the Occurrence of Rotavirus Gastroenteritis in Children < 5 Years of Age, in Bulgaria and Latvia
An Observational Study to Estimate the Disease Burden of Rotavirus Gastroenteritis in Infants/Children Less Than Five Years of Age in Primary Care Settings, in Bulgaria and Latvia
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
A Primary care setting will include independent general practitioners (GP) (specialised in paediatrics) or independent paediatricians.
Stool samples will be collected from all enrolled subjects at Visit 1 (Day 0) and tested immediately after collection. The stool sample will be stored for 24 hours only, in case the test cannot be performed immediately after collection.
Tipo de estudio
Inscripción (Actual)
Contactos y Ubicaciones
Ubicaciones de estudio
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Burgas, Bulgaria, 8000
- GSK Investigational Site
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Burgas, Bulgaria, 8018
- GSK Investigational Site
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Dobrich, Bulgaria, 9300
- GSK Investigational Site
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Pazardzik, Bulgaria, 4400
- GSK Investigational Site
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Pleven, Bulgaria, 5800
- GSK Investigational Site
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Plovdiv, Bulgaria, 4000
- GSK Investigational Site
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Ruse, Bulgaria, 7000
- GSK Investigational Site
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Sliven, Bulgaria, 8800
- GSK Investigational Site
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Sofia, Bulgaria, 1606
- GSK Investigational Site
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Sofia, Bulgaria, 1505
- GSK Investigational Site
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Sofia, Bulgaria, 1517
- GSK Investigational Site
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Sofia, Bulgaria, 1528
- GSK Investigational Site
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Stara Zagora, Bulgaria, 6000
- GSK Investigational Site
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Varna, Bulgaria, 9000
- GSK Investigational Site
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Veliko Turnovo, Bulgaria, 5000
- GSK Investigational Site
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Balvi, Letonia, LV-4501
- GSK Investigational Site
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Bauska, Letonia, LV-3901
- GSK Investigational Site
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Broceni, Letonia, LV-3851
- GSK Investigational Site
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Carnikava, Letonia, LV-2163
- GSK Investigational Site
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Daugavpils, Letonia, LV-5401
- GSK Investigational Site
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Daugavpils, Letonia, LV-5410
- GSK Investigational Site
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Druva, Letonia, LV-3862
- GSK Investigational Site
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Erglu pagasts, Letonia, LV-4840
- GSK Investigational Site
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Grobina, Letonia, LV-3430
- GSK Investigational Site
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Ikskile, Letonia, LV-5052
- GSK Investigational Site
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Jekabpils, Letonia, LV-5201
- GSK Investigational Site
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Jelgava, Letonia, LV-3001
- GSK Investigational Site
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Jelgava, Letonia, LV-3002
- GSK Investigational Site
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Jelgava, Letonia, LV-3007
- GSK Investigational Site
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Jelgava, Letonia, LV-3008
- GSK Investigational Site
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Kuldiga, Letonia, LV-3300
- GSK Investigational Site
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Liepaja, Letonia, LV-3401
- GSK Investigational Site
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Limbazi, Letonia, LV-4001
- GSK Investigational Site
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Livani, Letonia, LV-5316
- GSK Investigational Site
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Madona, Letonia, LV-4801
- GSK Investigational Site
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Ogre, Letonia, LV-5001
- GSK Investigational Site
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Ozolnieki, Letonia, LV-3018
- GSK Investigational Site
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Pinki, Letonia, LV-2107
- GSK Investigational Site
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Rezekne, Letonia, LV-4601
- GSK Investigational Site
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Rezekne, Letonia, LV-4604
- GSK Investigational Site
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Riga, Letonia, LV-1001
- GSK Investigational Site
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Riga, Letonia, LV-1002
- GSK Investigational Site
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Riga, Letonia, LV-1010
- GSK Investigational Site
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Riga, Letonia, LV-1011
- GSK Investigational Site
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Riga, Letonia, LV-1012
- GSK Investigational Site
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Riga, Letonia, LV-1024
- GSK Investigational Site
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Riga, Letonia, LV-1050
- GSK Investigational Site
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Riga, Letonia, LV-1063
- GSK Investigational Site
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Riga, Letonia, LV-1082
- GSK Investigational Site
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Ropazi, Letonia, LV-2135
- GSK Investigational Site
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Sigulda, Letonia, LV-2150
- GSK Investigational Site
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Tukums, Letonia, LV-3101
- GSK Investigational Site
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Valmiera, Letonia, LV-4200
- GSK Investigational Site
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Valmiera, Letonia, LV-4201
- GSK Investigational Site
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Vangazi, Letonia, LV-2136
- GSK Investigational Site
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Ventspils, Letonia, LV-3601
- GSK Investigational Site
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Ventspils, Letonia, LV-3602
- GSK Investigational Site
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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:
- Infants/children with home visits by the GPGP/paediatrician for the treatment of AGE or brought to the GP/paediatrician for AGE treatment during the study period.
- A male or female infant/child less than five years of age at the time of the GP/paediatrician visit. A child becomes ineligible on the day of her/his fifth birthday.
- Written informed consent obtained from the parents/legally acceptable representative (LARs) of the subject.
- Subjects who the investigator believes that his/her, parents/LARs can and will comply with the requirements of the protocol.
Exclusion Criteria:
• Child in care.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Modelos observacionales: Grupo
- Perspectivas temporales: Futuro
Cohortes e Intervenciones
Grupo / Cohorte |
Intervención / Tratamiento |
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Group Bulgaria
Subjects in this group include infants/children from Bulgaria, less than five years of age with home visits by the GP/paediatrician for the treatment of AGE or brought to the GP/paediatrician for the treatment of AGE.
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Samples will be tested to determine the presence or absence of rotavirus.
Log books
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Group Latvia
Subjects in this group include infants/children from Latvia, less than five years of age with home visits by the GP/paediatrician for the treatment of AGE or brought to the GP/paediatrician for the treatment of AGE.
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Samples will be tested to determine the presence or absence of rotavirus.
Log books
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Periodo de tiempo |
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Number of RV GE cases among the acute gastroenteritis (AGE) cases reported at primary care settings in infants/children less than five years of age.
Periodo de tiempo: At the time of enrollment of each subject (Day 0).
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At the time of enrollment of each subject (Day 0).
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Medidas de resultado secundarias
Medida de resultado |
Periodo de tiempo |
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Symptoms related to AGE and their measures, stratified by rotavirus status for all the AGE cases reported by infants/children less than five years of age at the primary care settings.
Periodo de tiempo: Day 0 - Day 14+5 (At the time of phone call follow-up contact).
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Day 0 - Day 14+5 (At the time of phone call follow-up contact).
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Number of RV GE cases reported at each month by infants/children less than five years of age reported at the primary care settings.
Periodo de tiempo: At the time of enrollment of each subject (Day 0).
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At the time of enrollment of each subject (Day 0).
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Number of hospitalisations for RV GE and AGE, reported at the primary care settings.
Periodo de tiempo: At the time of phone call follow-up contact (14 to 19 days after enrollment).
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At the time of phone call follow-up contact (14 to 19 days after enrollment).
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Colaboradores e Investigadores
Patrocinador
Publicaciones y enlaces útiles
Publicaciones Generales
- Tafalla M, Gardovska D, Gopala K, Kozlovska L. Primary care-based surveillance to estimate the proportion of rotavirus gastroenteritis among Latvian children below 5 years of age with acute gastroenteritis. Hum Vaccin Immunother. 2019;15(6):1272-1278. doi: 10.1080/21645515.2018.1534515. Epub 2018 Oct 31.
- Tiholova M, Gopala K, Berberova M, Strokova-Stoilova M, Tafalla M. Rotavirus gastroenteritis in children less than five years of age in primary care settings in Bulgaria: an observational study. Germs. 2016 Sep 1;6(3):97-105. doi: 10.11599/germs.2016.1095. eCollection 2016 Sep.
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
- 116621
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