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- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07737626
Effect of Powered Toothbrushing and Dental Flossing Sequence on Dental Plaque Removal
29 de julio de 2026 actualizado por: Sema Merve Altıngöz, Lokman Hekim University
Does the Sequence of Powered Toothbrushing and Dental Flossing Affect Dental Plaque Removal? A Randomized Crossover Clinical Trial
This randomized crossover clinical trial evaluated whether the sequence of powered toothbrushing and dental flossing affects dental plaque removal.
Forty-six systemically and periodontally healthy participants were randomly assigned to one of two oral hygiene sequences.
In Group 1, participants performed powered toothbrushing followed by dental flossing during the first period and dental flossing followed by powered toothbrushing during the second period.
Group 2 performed the same procedures in the opposite order.
The two intervention periods were separated by a 15-day washout period, with professional prophylaxis performed to standardize oral hygiene conditions.
Dental plaque was assessed before and after the oral hygiene procedures using the Plaque Index (PI) and the Turesky modification of the Quigley-Hein Plaque Index (TQHPI).
The study aimed to determine whether performing powered toothbrushing before or after dental flossing results in greater plaque removal.
Descripción general del estudio
Estado
Terminado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Intervencionista
Inscripción (Actual)
46
Fase
- No aplica
Contactos y Ubicaciones
Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.
Ubicaciones de estudio
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-
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Ankara, Turquía (Türkiye)
- Lokman Hekim University Faculty of Dentistry
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Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
Acepta Voluntarios Saludables
Sí
Descripción
Inclusion Criteria:
- Age between 18 and 30 years
- Systemically healthy
- Presence of at least 22 natural teeth
- No signs of active periodontal disease
- Ability to comply with the study procedures and oral hygiene instructions
- Provision of written informed consent
Exclusion Criteria:
- Antibiotic use within the previous 3 months
- Smoking
- Presence of systemic conditions known to affect periodontal health, including diabetes mellitus or immune-mediated disorders
- Ongoing orthodontic treatment
- Presence of fixed prostheses, crowns, or extensive restorations that could interfere with plaque assessment
- Professional periodontal therapy within the previous 3 months
- Pregnancy or lactation
- Severe dental crowding
Plan de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Prevención
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación cruzada
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: Brush-Floss Sequence (Group 1)
Participants assigned to this sequence will first perform powered toothbrushing followed by dental flossing during the first study period.
After the washout period, the order of the oral hygiene procedures will be reversed, with dental flossing performed before powered toothbrushing during the second study period.
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Participants will perform oral hygiene using a powered toothbrush according to the standardized study protocol.
The intervention will be applied as part of the assigned brushing-flossing sequence.
Participants will perform interdental cleaning using dental floss according to the standardized study protocol.
The intervention will be applied as part of the assigned brushing-flossing sequence.
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Experimental: Floss-Brush Sequence (Group 2)
Participants assigned to this sequence will first perform dental flossing followed by powered toothbrushing during the first study period.
After the washout period, the order of the oral hygiene procedures will be reversed, with powered toothbrushing performed before dental flossing during the second study period.
|
Participants will perform oral hygiene using a powered toothbrush according to the standardized study protocol.
The intervention will be applied as part of the assigned brushing-flossing sequence.
Participants will perform interdental cleaning using dental floss according to the standardized study protocol.
The intervention will be applied as part of the assigned brushing-flossing sequence.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Residual Plaque Index
Periodo de tiempo: Immediately after completion of the assigned oral hygiene sequence following 48 hours of plaque accumulation, in each study period.
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Residual dental plaque was assessed immediately after completion of the assigned oral hygiene sequence using the Plaque Index (PI).
Higher scores indicate greater residual plaque accumulation.
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Immediately after completion of the assigned oral hygiene sequence following 48 hours of plaque accumulation, in each study period.
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Residual Buccal Turesky Modified Quigley-Hein Plaque Index (TQHPI)
Periodo de tiempo: Immediately after completion of the assigned oral hygiene sequence following 48 hours of plaque accumulation, in each study period.
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Following plaque disclosure, residual plaque on the buccal tooth surfaces was assessed using the Turesky Modified Quigley-Hein Plaque Index (TQHPI), scored from 0 to 5, with higher scores indicating greater residual plaque accumulation.
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Immediately after completion of the assigned oral hygiene sequence following 48 hours of plaque accumulation, in each study period.
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Residual Lingual Turesky Modified Quigley-Hein Plaque Index (TQHPI)
Periodo de tiempo: Immediately after completion of the assigned oral hygiene sequence following 48 hours of plaque accumulation, in each study period.
|
Following plaque disclosure, residual plaque on the lingual tooth surfaces was assessed using the Turesky Modified Quigley-Hein Plaque Index (TQHPI), scored from 0 to 5, with higher scores indicating greater residual plaque accumulation.
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Immediately after completion of the assigned oral hygiene sequence following 48 hours of plaque accumulation, in each study period.
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Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio (Actual)
2 de mayo de 2026
Finalización primaria (Actual)
15 de julio de 2026
Finalización del estudio (Actual)
15 de julio de 2026
Fechas de registro del estudio
Enviado por primera vez
27 de julio de 2026
Primero enviado que cumplió con los criterios de control de calidad
29 de julio de 2026
Publicado por primera vez (Actual)
30 de julio de 2026
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
30 de julio de 2026
Última actualización enviada que cumplió con los criterios de control de calidad
29 de julio de 2026
Última verificación
1 de julio de 2026
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- LHU-2026-164
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
NO
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
No
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
No
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. .