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Clinical Performance and Psychological Impact of Colored Restorations Cement in Primary Molars

27 de septiembre de 2022 actualizado por: Nadia Metwalli, British University In Egypt

Clinical Performance and Psychological Impact of Colored Poly-acid Modified Composite Resin Versus Glass Ionomer Cement in Primary Molars: an RCT Study

Aim of the study

The aim of the presented study is to evaluate:

I- The clinical performance of flowable polyacid-modified composite resin 'compomer' and resin-modified glass-ionomer cement in prepared Class II cavities in primary molars over a period of 6 months.

II- Psychological impact of the coloured material used on the child's behavior towards the dental procedure.

Materials and Methods Forty primary molars from healthy children between ages of four and seven years will be included in this study, parents will be asked to sign an informed consent on behalf of the children. Statistical power analysis was performed using G-power program. An alpha type error of 0.05, a beta power of 0.95 and a N2/N1 ratio of 1 was used. This study have the approval of the research ethics committee BUE. This study will be executed in the Faculty of Dentistry, BUE, Department of Pediatric Dentistry. Subjects will be selected from children who are seeking dental treatment at the Pediatric Dentistry and Dental Public Health clinic in the Faculty of Dentistry, BUE. Children with detectable caries for Class II cavity preparation will be classified randomly under the different treatment groups. Group A: Colored polyacid modified composite resin , Group B: Glass ionomer cement All groups will be restored according to material used. Restorations will be assessed for marginal adaptation, marginal discoloration, anatomic form, and secondary caries. The assessment of all restorations will be carried out at 24-hours, 3, 6 months post-operatively under normal clinical conditions with a dental operating light, a mouth mirror and a dental explorer. The impact of the color of the material used on the child's attitude will be assessed once through a questionnaire given to the child at the beginning of the first dental visit in which each child will be asked to choose from pictures that indicate their preference regarding the use of colored and non-colored restorative materials and how their choice will affect their attitude whether they will be happy, sad or neutral.

As per the scheduled follow up visits, these are the regular follow up intervals for any child undergoing dental treatment. Accordingly, it won't be of an extra burden on the patient/ parent.

Statistical analysis Data will be collected, tabulated and statistically analyzed using statistical package for Social Science (SPSS 15.0.1 for windows; SPSS Inc, Chicago, IL, 2001). Data will be presented and suitable analysis will be done according to the type of data obtained for each parameter.

Descripción general del estudio

Estado

Terminado

Intervención / Tratamiento

Descripción detallada

Aim of the study

The aim of the presented study is to evaluate:

I- The clinical performance of flowable polyacid-modified composite resin 'compomer' and resin-modified glass-ionomer cement in prepared Class II cavities in primary molars over a period of 6 months.

II- Psychological impact of the coloured material used on the child's behavior towards the dental procedure.

Materials and Methods Forty primary molars from children between ages of four and seven years will be included in this study, parents will be asked to sign an informed consent on behalf of the children. Statistical power analysis was performed using G-power program. An alpha type error of 0.05, a beta power of 0.95 and a N2/N1 ratio of 1 was used. This study will have the approval of the research ethics committee BUE and will be registered in clinical trial website.

This study will be executed in the Faculty of Dentistry, ,BUE,Department of Pediatric Dentistry. Subjects will be selected from children who are seeking dental treatment at the Pediatric Dentistry and Dental Public Health clinic in the Faculty of Dentistry, BUE. Children with detectable caries for Class II cavity preparation will be classified randomly under the different treatment groups.

Group A: Colored polyacid modified composite resin Group B: Glass ionomer cement

Children will be recruited according to the following inclusion and exclusion criteria:

Table 1: Inclusion and exclusion criteria Inclusion criteria Exclusion criteria Radiographic examination (bite-wing radiograph) showing evidence of proximal caries. Radiographic examination (bite-wing radiograph) showing evidence of occlusal caries only, or showing evidence of proximal caries extending to the pulp.

Proximal contact with adjacent healthy or restored tooth. Isolated tooth No signs or symptoms of pulp involvement Signs or symptom of pulp involvement.

No signs of periapical pathosis Signs of periapical pathosis No signs of periodontal involvement Signs of periodontal involvement 2 years at least till normal exfoliation Less than 2 years for exfoliation 2/3 of the root is still present Less than 2/3 of the root is present No restoration present Restoration present No cuspal involvement Cuspal involvement

All groups will be restored according to material used. Restorations will be assessed for marginal adaptation, marginal discoloration, anatomic form, and secondary caries. The assessment of all restorations will be carried out at 24-hours, 3, 6 months post-operatively under normal clinical conditions with a dental operating light, a mouth mirror and a dental explorer.

The impact of the color of the material used on the child's attitude will be assessed once through a questionnaire given to the child at the beginning of the first dental visit in which each child will be asked to choose from pictures that indicate their preference regarding the use of colored and non-colored restorative materials and how their choice will affect their attitude whether they will be happy, sad or neutral.

It is worth mentioning that the children selected for this study will be given meticulous oral hygiene measures instructions and will undergo full dental treatment during the course of the study thus, there are absolutely no risks on the human participants especially that only the decayed molars will be filled using the two different materials used in this study. However, chances of loss of the filling material, secondary caries, loss of the anatomical form, marginal discolouration and loss of the marginal adaptation might still be a subject of concern.

If these materials have been proved to be durable, more accepted by the children and less technique sensitive to the clinician then the patient/parent will be informed by the results and given the choice in case he/she wishes to change the restoration at any point and time.

As per the scheduled follow up visits, these are the regular follow up intervals for any child undergoing dental treatment. Accordingly, it won't be of an extra burden on the patient/ parent.

Statistical analysis Data will be collected, tabulated and statistically analyzed using statistical package for Social Science (SPSS 15.0.1 for windows; SPSS Inc, Chicago, IL, 2001). Data will be presented and suitable analysis will be done according to the type of data obtained for each parameter.

  1. Descriptive Statistics: frequency and percentage of non-numerical data
  2. Analytical Statistics: The Cochran Q procedure tests the null hypothesis that multiple related proportions are the same. The Cochran test is a multivariate extension of the McNemar test used for two related samples.

Tipo de estudio

De observación

Inscripción (Actual)

40

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

      • Cairo, Egipto
        • The British University in Egypt

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

4 años a 7 años (Niño)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Método de muestreo

Muestra no probabilística

Población de estudio

Healthy children between ages of four and seven years will be included in this study

Descripción

Inclusion Criteria:

  • Radiographic examination (bite-wing radiograph) showing evidence of proximal caries.
  • Proximal contact with adjacent healthy or restored tooth.
  • No signs or symptoms of pulp involvement
  • No signs of periapical pathosis
  • No signs of periodontal involvement
  • 2 years at least till normal exfoliation
  • 2/3 of the root is still present
  • No restoration present
  • No cuspal involvement

Exclusion Criteria:

  • Radiographic examination (bite-wing radiograph) showing evidence of occlusal caries only, or showing evidence of proximal caries extending to the pulp.
  • Isolated tooth
  • Signs or symptom of pulp involvement.
  • Signs of periapical pathosis
  • Signs of periodontal involvement
  • Less than 2 years for exfoliation
  • Less than 2/3 of the root is present
  • Cuspal involovement
  • Restoration present

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

  • Modelos observacionales: Control de caso
  • Perspectivas temporales: Futuro

Cohortes e Intervenciones

Grupo / Cohorte
Intervención / Tratamiento
clinical performance
restoration of caries primary molars using two different restorative materials
Restorative treatment using dental materials
Otros nombres:
  • glass ionomer restorative treatment
psychological impact
evaluation of colour of restoration on the satisfaction of the children and impact on their hygiene

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
healing
Periodo de tiempo: 3 months post-operatively
The assessment of all restorations will be carried out at 24-hours operatively under normal clinical conditions with a dental operating light, a mouth mirror and a dental explorer.
3 months post-operatively
healing
Periodo de tiempo: 3 months post-operatively
The assessment of all restorations will be carried out at 3 months operatively under normal clinical conditions with a dental operating light, a mouth mirror and a dental explorer.
3 months post-operatively
healing
Periodo de tiempo: 6 months post-operatively
The assessment of all restorations will be carried out at 6 months operatively under normal clinical conditions with a dental operating light, a mouth mirror and a dental explorer.
6 months post-operatively

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
impact of colour
Periodo de tiempo: 24-hours, 3, 6 months post-operatively
assessed once through a questionnaire given to the child at the beginning of the first dental visit in which each child will be asked to choose from pictures that indicate their preference regarding the use of colored and non-colored restorative materials and how their choice will affect their attitude whether they will be happy, sad or neutral.
24-hours, 3, 6 months post-operatively
impact of colour
Periodo de tiempo: 3 months post-operatively
assessed once through a questionnaire given to the child at the beginning of the first dental visit in which each child will be asked to choose from pictures that indicate their preference regarding the use of colored and non-colored restorative materials and how their choice will affect their attitude whether they will be happy, sad or neutral.
3 months post-operatively
impact of colour
Periodo de tiempo: 6 months post-operatively
assessed once through a questionnaire given to the child at the beginning of the first dental visit in which each child will be asked to choose from pictures that indicate their preference regarding the use of colored and non-colored restorative materials and how their choice will affect their attitude whether they will be happy, sad or neutral.
6 months post-operatively

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

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 noviembre de 2021

Finalización primaria (Actual)

1 de abril de 2022

Finalización del estudio (Actual)

1 de mayo de 2022

Fechas de registro del estudio

Enviado por primera vez

2 de febrero de 2022

Primero enviado que cumplió con los criterios de control de calidad

27 de septiembre de 2022

Publicado por primera vez (Actual)

28 de septiembre de 2022

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

28 de septiembre de 2022

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

27 de septiembre de 2022

Última verificación

1 de septiembre de 2022

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • FDBUEREC21-30

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. .

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