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Microbial Contamination of Different Toothbrush Types Stored in Bathrooms and Rooms in Adolescents

8 de noviembre de 2026 actualizado por: Özgür Doğan, Afyonkarahisar Health Sciences University

Microbial Contamination of Silver Nanoparticle, Bamboo Charcoal and Standard Toothbrushes Stored in Bathroom Versus Room Environments: A Randomized Clinical Study in Adolescents

This randomized clinical study aimed to compare microbial contamination of three different toothbrush types (standard plastic, silver nanoparticle, and bamboo charcoal) and to investigate whether storing toothbrushes in a bathroom or a room outside the bathroom affects microbial contamination.

The study included 72 healthy adolescents aged 11-18 years who were undergoing removable orthodontic appliance treatment. Participants were randomly assigned to one of three toothbrush groups and two storage conditions (bathroom or room). All participants received standardized oral hygiene instructions and used their assigned toothbrushes twice daily for one month.

After one month, the toothbrushes were collected and examined for the presence of three microorganisms: *Streptococcus mutans*, *Lactobacillus* spp., and *Candida albicans*. In addition, plaque index, gingival index, probing depth, and bleeding on probing were assessed at baseline and after one month.

The study was designed to determine whether toothbrushes marketed as having antimicrobial properties and different storage environments influence microbial contamination and short-term periodontal health.

Descripción general del estudio

Descripción detallada

This randomized, parallel-group clinical study was conducted at Afyonkarahisar Health Sciences University, Türkiye, between March 2021 and July 2022. The study investigated the effects of toothbrush type and storage environment on microbial contamination under routine home-use conditions.

Participants were randomly allocated to three toothbrush groups: standard plastic (Colgate Extra Clean), silver nanoparticle (Splat Sensitive Silver), and bamboo charcoal (Colgate Bamboo Charcoal). Each group was further divided into two storage subgroups: bathroom storage and room storage outside the bathroom. Randomization was performed using colored balls drawn by an investigator who was not involved in clinical or microbiological assessments. The microbiologist was blinded to group allocation.

At baseline, all participants received professional prophylaxis and standardized oral hygiene instructions. Participants were instructed to brush twice daily for two minutes using the modified Stillman technique and the same fluoride toothpaste. After brushing, toothbrushes were rinsed under tap water and stored upright and uncovered in the assigned environment. Toothbrushes were not shared or stored in contact with other toothbrushes.

After one month, the used toothbrushes were collected in sterile bags. Under aseptic conditions, one-third of the bristles were removed and transferred into thioglycolate broth. Samples were transported under refrigerated conditions to the microbiology laboratory. Following broth enrichment, samples were cultured on selective media to detect *Streptococcus mutans*, *Lactobacillus* spp., and *Candida albicans*. Suspected isolates were identified using the VITEK 2 Compact system.

Microbial contamination was evaluated based on the presence or absence of each target microorganism rather than quantitative bacterial counts.

Clinical periodontal assessments were performed at baseline and after one month using standardized measurements of plaque index, gingival index, probing depth, and bleeding on probing.

The study was approved by the Clinical Research Ethics Committee of Afyonkarahisar Health Sciences University (approval number: 2020/13; November 6, 2020). Written informed consent was obtained from parents or legal guardians, and assent was obtained from participants.

Tipo de estudio

Intervencionista

Inscripción (Actual)

72

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

      • Afyonkarahisar, Turquía (Türkiye)
        • Afyonkarahisar Health Sciences University

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

11 años a 18 años (Niño, Adulto)

Acepta Voluntarios Saludables

Sí

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • Adolescents aged 11-18 years.
  • Systemically healthy individuals.
  • Patients undergoing dentofacial orthopedic treatment with removable functional appliances.

Exclusion Criteria:

  • Use of systemic antibiotics within the previous 3 months.
  • Use of antimicrobial mouthwash within the previous 3 months.
  • Presence of systemic disease.
  • Smoking.

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 factorial
  • Enmascaramiento: Único

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Comparador activo: Standard Toothbrush - Bathroom

Participants assigned to this arm used a standard plastic toothbrush (Colgate Extra Clean) twice daily for two minutes using the modified Stillman brushing technique and standardized fluoride toothpaste. After each use, the toothbrush was rinsed under tap water and stored upright and uncovered in the bathroom. The intervention lasted one month, after which the toothbrush was collected for microbiological analysis.

A commercially available standard plastic toothbrush (Colgate Extra Clean, Colgate-Palmolive Company, New York, NY, USA) was used as the active comparator. Participants brushed their teeth twice daily for two minutes using the modified Stillman technique and standardized fluoride toothpaste for one month. After each use, the toothbrush was rinsed under tap water and stored upright and uncovered in the assigned storage environment (bathroom or room outside the bathroom). At the end of the intervention period, toothbrushes were collected for microbiological analysis.

Comparador activo: Standard Toothbrush - Room

Participants assigned to this arm used a standard plastic toothbrush (Colgate Extra Clean) twice daily for two minutes using the modified Stillman brushing technique and standardized fluoride toothpaste. After each use, the toothbrush was rinsed under tap water and stored upright and uncovered in a room outside the bathroom. The intervention lasted one month, after which the toothbrush was collected for microbiological analysis.

A commercially available standard plastic toothbrush (Colgate Extra Clean, Colgate-Palmolive Company, New York, NY, USA) was used as the active comparator. Participants brushed their teeth twice daily for two minutes using the modified Stillman technique and standardized fluoride toothpaste for one month. After each use, the toothbrush was rinsed under tap water and stored upright and uncovered in the assigned storage environment (bathroom or room outside the bathroom). At the end of the intervention period, toothbrushes were collected for microbiological analysis.

Experimental: Silver Nanoparticle Toothbrush - Bathroom

Participants assigned to this arm used a silver nanoparticle-containing toothbrush (Splat Sensitive Silver) twice daily for two minutes using the modified Stillman brushing technique and standardized fluoride toothpaste. After each use, the toothbrush was rinsed under tap water and stored upright and uncovered in the bathroom. The intervention lasted one month, after which the toothbrush was collected for microbiological analysis.

A commercially available silver nanoparticle-containing toothbrush (Splat Sensitive Silver, SPLAT-COSMETICA, Moscow, Russia) was used to evaluate microbial contamination compared with a standard plastic toothbrush. Participants brushed their teeth twice daily for two minutes using the modified Stillman technique and standardized fluoride toothpaste for one month. After each use, the toothbrush was rinsed under tap water and stored upright and uncovered in the assigned storage environment (bathroom or room outside the bathroom). At the end of the intervention period, toothbrushes were collected for microbiological analysis.

Experimental: Silver Nanoparticle Toothbrush - Room

Participants assigned to this arm used a silver nanoparticle-containing toothbrush (Splat Sensitive Silver) twice daily for two minutes using the modified Stillman brushing technique and standardized fluoride toothpaste. After each use, the toothbrush was rinsed under tap water and stored upright and uncovered in a room outside the bathroom. The intervention lasted one month, after which the toothbrush was collected for microbiological analysis.

A commercially available silver nanoparticle-containing toothbrush (Splat Sensitive Silver, SPLAT-COSMETICA, Moscow, Russia) was used to evaluate microbial contamination compared with a standard plastic toothbrush. Participants brushed their teeth twice daily for two minutes using the modified Stillman technique and standardized fluoride toothpaste for one month. After each use, the toothbrush was rinsed under tap water and stored upright and uncovered in the assigned storage environment (bathroom or room outside the bathroom). At the end of the intervention period, toothbrushes were collected for microbiological analysis.

Experimental: Bamboo Charcoal Toothbrush - Bathroom

Participants assigned to this arm used a bamboo charcoal toothbrush (Colgate Bamboo Charcoal) twice daily for two minutes using the modified Stillman brushing technique and standardized fluoride toothpaste. After each use, the toothbrush was rinsed under tap water and stored upright and uncovered in the bathroom. The intervention lasted one month, after which the toothbrush was collected for microbiological analysis.

A commercially available bamboo charcoal toothbrush (Colgate Bamboo Charcoal, Colgate-Palmolive Company, New York, NY, USA) was used to evaluate microbial contamination compared with a standard plastic toothbrush. Participants brushed their teeth twice daily for two minutes using the modified Stillman technique and standardized fluoride toothpaste for one month. After each use, the toothbrush was rinsed under tap water and stored upright and uncovered in the assigned storage environment (bathroom or room outside the bathroom). At the end of the intervention period, toothbrushes were collected for microbiological analysis.

Experimental: Bamboo Charcoal Toothbrush - Room

Participants assigned to this arm used a bamboo charcoal toothbrush (Colgate Bamboo Charcoal) twice daily for two minutes using the modified Stillman brushing technique and standardized fluoride toothpaste. After each use, the toothbrush was rinsed under tap water and stored upright and uncovered in a room outside the bathroom. The intervention lasted one month, after which the toothbrush was collected for microbiological analysis.

A commercially available bamboo charcoal toothbrush (Colgate Bamboo Charcoal, Colgate-Palmolive Company, New York, NY, USA) was used to evaluate microbial contamination compared with a standard plastic toothbrush. Participants brushed their teeth twice daily for two minutes using the modified Stillman technique and standardized fluoride toothpaste for one month. After each use, the toothbrush was rinsed under tap water and stored upright and uncovered in the assigned storage environment (bathroom or room outside the bathroom). At the end of the intervention period, toothbrushes were collected for microbiological analysis.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Presence of Streptococcus mutans on Toothbrushes
Periodo de tiempo: 1 month after baseline (end of toothbrush use)

The presence or absence of Streptococcus mutans on toothbrush bristles was assessed after one month of use. Bristle samples were cultured on selective Mitis Salivarius agar supplemented with bacitracin and potassium tellurite following broth enrichment. Suspected isolates were identified using the VITEK 2 Compact system. The outcome was recorded as a binary variable (detected/not detected), and the proportion of contaminated toothbrushes was compared across toothbrush types and storage environments.

1 month after baseline (end of toothbrush use)
Presence of Lactobacillus spp. on Toothbrushes
Periodo de tiempo: 1 month after baseline (end of toothbrush use)

The presence or absence of Lactobacillus spp. on toothbrush bristles was assessed after one month of use. Bristle samples were cultured on Rogosa agar adjusted to pH 5.5 following broth enrichment. Suspected isolates were identified using the VITEK 2 Compact system. The outcome was recorded as a binary variable (detected/not detected), and the proportion of contaminated toothbrushes was compared across toothbrush types and storage environments.

1 month after baseline (end of toothbrush use)
Presence of Candida albicans on Toothbrushes
Periodo de tiempo: 1 month after baseline (end of toothbrush use)

The presence or absence of Candida albicans on toothbrush bristles was assessed after one month of use. Bristle samples were cultured on Sabouraud dextrose agar supplemented with chloramphenicol following broth enrichment. Suspected isolates were identified using the VITEK 2 Compact system. The outcome was recorded as a binary variable (detected/not detected), and the proportion of contaminated toothbrushes was compared across toothbrush types and storage environments.

1 month after baseline (end of toothbrush use)

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in Plaque Index From Baseline to One Month
Periodo de tiempo: Baseline and 1 month

Dental plaque accumulation was assessed using the Silness and Löe Plaque Index at baseline and after one month of toothbrush use. The change in plaque index was calculated by subtracting the baseline score from the one-month score. Changes were compared across toothbrush types and storage environments. Lower scores indicate less plaque accumulation.

Baseline and 1 month
Change in Gingival Index From Baseline to One Month
Periodo de tiempo: Baseline and 1 month

Gingival inflammation was assessed using the Löe and Silness Gingival Index at baseline and after one month of toothbrush use. The change in gingival index was calculated by subtracting the baseline score from the one-month score. Changes were compared across toothbrush types and storage environments. Lower scores indicate less gingival inflammation.

Baseline and 1 month
Change in Buccal Probing Depth From Baseline to One Month
Periodo de tiempo: Baseline and 1 month

Buccal periodontal probing depth was measured in millimeters using a periodontal probe (Hu-Friedy No. 15) at baseline and after one month of toothbrush use. Measurements were obtained as part of a standardized six-site periodontal examination of all teeth present. The change in buccal probing depth was calculated by subtracting the baseline value from the one-month value. Changes were compared across toothbrush types and storage environments. Positive values indicate an increase in probing depth.

Baseline and 1 month
Change in Lingual Probing Depth From Baseline to One Month
Periodo de tiempo: Baseline and 1 month

Lingual periodontal probing depth was measured in millimeters using a periodontal probe (Hu-Friedy No. 15) at baseline and after one month of toothbrush use. Measurements were obtained as part of a standardized six-site periodontal examination of all teeth present. The change in lingual probing depth was calculated by subtracting the baseline value from the one-month value. Changes were compared across toothbrush types and storage environments. Positive values indicate an increase in probing depth.

Baseline and 1 month
Change in Bleeding on Probing From Baseline to One Month
Periodo de tiempo: Baseline and 1 month

Bleeding on probing (BOP) was assessed at six sites per tooth using a periodontal probe (Hu-Friedy No. 15) at baseline and after one month of toothbrush use. BOP was expressed as the percentage of examined sites exhibiting bleeding. The change in BOP was calculated by subtracting the baseline percentage from the one-month percentage and was expressed in percentage points. Changes were compared across toothbrush types and storage environments. Negative values indicate a reduction in gingival bleeding.

Baseline and 1 month

Colaboradores e Investigadores

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Publicaciones y enlaces útiles

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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)

1 de marzo de 2021

Finalización primaria (Actual)

16 de agosto de 2022

Finalización del estudio (Actual)

4 de septiembre de 2022

Fechas de registro del estudio

Enviado por primera vez

8 de noviembre de 2026

Primero enviado que cumplió con los criterios de control de calidad

8 de noviembre de 2026

Publicado por primera vez (Actual)

13 de noviembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

13 de noviembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

8 de noviembre de 2026

Última verificación

1 de noviembre de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • Seher Gözde Uğur
  • 21.DUS.001 (Otro número de subvención/financiamiento: Afyonkarahisar Health Sciences University - Scientific Research Projects Coordination Unit)

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan IPD

Individual participant data (IPD) will not be made publicly available due to participant confidentiality and privacy considerations, as the study involved adolescents. The study was conducted under institutional ethical approval, and no formal IPD sharing plan was established.

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. .

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