- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT04223544
Incidence of Influenza Infections and Determination of Vaccination Coverage Rate Among Healthcare Workers
Incidence of Influenza Infections and Determination of Vaccination Coverage Rate Among Hospital and GPs Healthcare Workers During the 2019/2020 Epidemic Season
The main aim of research is to determine of the prevalence of influenza virus and influenza vaccination coverage rate among hospital and GPs healthcare workers.
Course of research:
Participation in the study is voluntary and carried out after the consent of the examined person. The examination consists of: 1) completing the questionnaire and 2) taking the throat swab twice by the researcher. Two throat swab samples will be taken at the same time. Both samples will be used for virological examination to determine the presence of influenza virus material using non-invasive tests: one sample will be analyzed by a quick 'on-site' test - Flu SensDx kit, while the other sample will be transported to the laboratory, where the reverse transcriptase polymerase chain reaction (RT-PCR) - reference method - will be performed to confirm the presence of influenza genetic material. Swabs are planned to be collected during the 2019/2020 influenza epidemic season (January-March).
In the last stage of the study, the results obtained from the survey questionnaire and the results of virological tests will be subject to statistical analysis and based on the data obtained, conclusions will be drawn from the study, indicating their practical application.
The results obtained from this study will be used to develop a quality improvement program to control influenza virus infection, which will improve the safety of both patients and medical staff.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Anticipado)
Contactos y Ubicaciones
Ubicaciones de estudio
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Wrocław, Polonia, 51-141
- Reclutamiento
- Family Medicine Department of Wroclaw Medical University
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Contacto:
- Michal Jedrzejek
- Número de teléfono: +48691399392
- Correo electrónico: michaljedrzejek@gmail.com
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Niño
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Método de muestreo
Población de estudio
Descripción
Inclusion Criteria:
- Healthcare worker of selected General Practices or hospitals wards
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
Cohortes e Intervenciones
Grupo / Cohorte |
Intervención / Tratamiento |
|---|---|
|
GPs Healthcare Workers
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Participation in the study is voluntary and carried out after the consent of the examined person.
The examination consists of: 1) completing the questionnaire and 2) taking the throat swab twice by the researcher.
Two throat swab samples will be taken at the same time.
Both samples will be used for virological examination to determine the presence of influenza virus material using non-invasive tests: one sample will be analyzed by a quick 'on-site' test - Flu SensDx kit, while the other sample will be transported to the laboratory, where the reverse transcriptase polymerase chain reaction (RT-PCR) - reference method - will be performed to confirm the presence of influenza genetic material.
Swabs are planned to be collected during the 2019/2020 influenza epidemic season (January-March).
|
|
Hospital Healthcare Workers
|
Participation in the study is voluntary and carried out after the consent of the examined person.
The examination consists of: 1) completing the questionnaire and 2) taking the throat swab twice by the researcher.
Two throat swab samples will be taken at the same time.
Both samples will be used for virological examination to determine the presence of influenza virus material using non-invasive tests: one sample will be analyzed by a quick 'on-site' test - Flu SensDx kit, while the other sample will be transported to the laboratory, where the reverse transcriptase polymerase chain reaction (RT-PCR) - reference method - will be performed to confirm the presence of influenza genetic material.
Swabs are planned to be collected during the 2019/2020 influenza epidemic season (January-March).
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Incidence of Influenza Infections
Periodo de tiempo: January-March 2020
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Incidence of influenza will be determined of results of POC and laboratory testing
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January-March 2020
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Vaccination Coverage Rate
Periodo de tiempo: January-March 2020
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Vaccination Coverage Rate will be determined of survey questionnaires
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January-March 2020
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Michal Jedrzejek, Family Medicine Department of Wroclaw Medical University
Publicaciones y enlaces útiles
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Anticipado)
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 (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
Otros números de identificación del estudio
- 779/2019
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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