- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07859553
Powered vs Manual Toothbrush Use: Its Effect on Caries Risk in Pre-Adolescents
Powered vs Manual Toothbrush Use: Its Effect on Caries Risk in Pre-Adolescents, A Pilot Study
This pilot study aims to evaluate dental caries experience in children ages 8-12 years old through comparing the use of a powered versus manual toothbrush, while using a standardized fluoride toothpaste as the control over the course of one year.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Estimado)
Fase
- No aplica
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Taylor Cezon, RDH
- Número de teléfono: 734-730-8533
- Correo electrónico: kidscavities@umich.edu
Ubicaciones de estudio
-
-
Michigan
-
Ann Arbor, Michigan, Estados Unidos, 48109
- Reclutamiento
- University of Michigan
-
Investigador principal:
- Margherita Fontana, DDS, PhD
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
-
Child:
- Male OR Female, between 8 - 12 years old at baseline
- In good health (i.e., free of any medical condition that would reasonably be anticipated to interfere with study participation)
- Must allow examination of the oral cavity at baseline
- Must have at least an ICDAS 2 or higher at baseline or radiographic signs of untreated caries lesions E2 or higher, or caries experience in the last 3 years (extraction due to caries, restoration due to caries, etc.)
- Able to tolerate radiographs
- Able to brush teeth by themselves with no assistance
Parent/Legal Guardian:
- Provide written informed consent for the child and her/himself prior to participation
- Must be at least 18 years old, or an emancipated minor who provides documentation of emancipation
- Must be willing and able to participate in study activities
Exclusion Criteria:
-
Child:
- Hereditary generalized developmental dental defects such as Amelogenesis Imperfecta and Dentinogenesis Imperfecta
- Presence of pain, pulpal exposure, or signs of pulpal infection (abscess, fistula, swelling) at baseline
- Participating in the foster care system
- Demonstrated inability to comply with study protocol requirements (including radiographs or abstaining from using other oral hygiene products such as mouth rinses during the study period)
- Has removable OR fixed orthodontic appliances
- Participation (within 30 days of Baseline Visit) in any other oral hygiene clinical study
Parent/Legal Guardian:
• Demonstrated inability to comply with trial protocol requirements
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Prevención
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Sin intervención: Manual Toothbrush
|
|
|
Experimental: Powered Toothbrush
|
Powered toothbrush Oral-B iO Kids Electric Toothbrush Featuring Stitch |
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Number of new caries surfaces and number of progressed caries surfaces
Periodo de tiempo: 12 Months
|
Composite Endpoint. New caries surface defined as baseline was sound (ICDAS=0 and no filling) and follow-up was enamel or dentin decay (ICDAS≥1), filling, or extracted due to caries. Caries progression defined if baseline was enamel decay and follow-up was dentin decay, filling, or extracted due to caries. |
12 Months
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Number of new caries surfaces
Periodo de tiempo: 12 Months
|
New caries surface defined as baseline was sound (ICDAS=0 and no filling) and follow-up was enamel or dentin decay (ICDAS≥1), filling, or extracted due to caries. |
12 Months
|
|
Number of new caries surfaces and number of progressed caries surfaces
Periodo de tiempo: 6 Months
|
Composite Endpoint. New caries surface defined as baseline was sound (ICDAS=0 and no filling) and follow-up was enamel or dentin decay (ICDAS≥1), filling, or extracted due to caries. Caries progression defined if baseline was enamel decay and follow-up was dentin decay, filling, or extracted due to caries. |
6 Months
|
|
Number of new caries surfaces
Periodo de tiempo: 6 Months
|
New caries surface defined as baseline was sound (ICDAS=0 and no filling) and follow-up was enamel or dentin decay (ICDAS≥1), filling, or extracted due to caries. |
6 Months
|
Colaboradores e Investigadores
Patrocinador
Colaboradores
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
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
- HUM00295963
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Descripción del plan IPD
Interested parties and contact the PI for potential collaboration
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.
producto fabricado y exportado desde los EE. UU.
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