Clinical Trial NuSmile Crowns
A Clinical Trial of NuSmile's Pre-Veneered Stainless Steel Crowns and NuSmile ZR Crowns Compared With Strip Composite Crowns in Anterior Primary Teeth -- Pilot Study
Descripción general del estudio
Estado
Intervención / Tratamiento
Descripción detallada
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
-
-
Washington
-
Seattle, Washington, Estados Unidos, 98115
- University of Washington-The Center for Pediatric Dentistry
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Patients of record at the University of Washington's Center for Pediatric Dentistry
- Patients in general good health (ASA I)
- Patients aged 5 years old or younger
- Patients in need of at least one preformed crowns, on anterior primary teeth
- Patients undergoing general anesthesia for dental treatment
- Parent or guardian of patient able and willing to provide informed consent
Exclusion Criteria:
- Medically compromising condition
- Teeth with proximal space closures of sufficient magnitude to preclude placement of crown
- Teeth with complete absence of facial or lingual walls following tooth preparation
- Teeth that are expected to be exfoliated/extracted within one year will not participate in the study
- Anterior crowding
- Occlusion class III
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Comparador activo: Nu Smile Zirconia crown
Anterior primary teeth which received a NuSmile zirconia crown as a final restoration
|
Placement of an anterior primary crown restoration
|
|
Comparador activo: Nu Smile pre veneered crown
Anterior primary teeth which received a NuSmile pre veneered crown as a final restoration
|
Placement of an anterior primary crown restoration
|
|
Comparador activo: Composite strip crown
Anterior primary teeth which received a composite strip crown as a final restoration
|
Placement of an anterior primary crown restoration
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Fitting
Periodo de tiempo: 12 months
|
The number of teeth scored in the crown fitting categories described below Fitting 0 = Good natural retention
A higher score means a worse outcome |
12 months
|
|
Positioning
Periodo de tiempo: 12 months
|
Change in the following clinical assessment measure between baseline and 12 months using the categories below Positioning 0= Proper position
A higher score means a worse outcome |
12 months
|
|
Proximal Contact
Periodo de tiempo: 12 months
|
The number of teeth scored in the proximal contact categories as described below Proximal contact 0= Open spaces
A higher score means a worse outcome |
12 months
|
|
Marginal Adaptation
Periodo de tiempo: 12 months
|
The number of teeth scored in the marginal adaptation categories as described below Marginal adaptation 0= No discrepancies detected with explorer
A higher score means a worse outcome |
12 months
|
|
Color
Periodo de tiempo: 12 months
|
The number of teeth scored in the color categories described below Color matching 0= Matches completely or within range of shade and translucency
A higher score means a worse outcome |
12 months
|
|
Gingival Status
Periodo de tiempo: 12 months
|
The number of teeth scored in the gingival status categories described below Gingival status 0=Pink, firm, free of inflammation
A higher score means a worse outcome |
12 months
|
|
Retention of the Crown
Periodo de tiempo: 12 months
|
The number of teeth scored in the retention of the crown categories described below Retention of the crown 0= Intact 1= Partially missing 2 = Missing - some cement remaining on both tooth and crown interior A higher score means a worse outcome |
12 months
|
|
Integrity of the Veneer/Composite
Periodo de tiempo: 12 months
|
The number of teeth scored in the integrity of the veneer/composite categories described below Integrity of veneer/ composite 0= Intact
A higher score means a worse outcome |
12 months
|
|
Secondary Caries
Periodo de tiempo: 12 months
|
The number of teeth scored in the secondary caries categories described below Secondary caries 0= Absent 1= Present A higher score means a worse outcome |
12 months
|
|
History of Trauma
Periodo de tiempo: 12 months
|
The number of teeth scored in the history of trauma categories described below History of trauma 0= Absent 1= Present A higher score means a worse outcome |
12 months
|
|
Clinical Pulp Pathology
Periodo de tiempo: 12 months
|
The number of teeth scored in the clinical pulp pathology categories described below Clinical pulp pathology 0= Absent 1= Present A higher score means a worse outcome |
12 months
|
|
Radiographical Pulp Pathology
Periodo de tiempo: 12 months
|
The number of teeth scored in the radiographical pulp pathology categories described below Radiographical pulp pathology 0= Absent 1= Present A higher score means a worse outcome A higher score means a worse outcome |
12 months
|
|
Parent's Esthetic Satisfaction
Periodo de tiempo: 12 months
|
The number of teeth scored in the parent's esthetic satisfaction categories described below Parents esthetic satisfaction via a survey 0=Satisfied 1= Dissatisfied A higher score means a worse outcome |
12 months
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Mariella Garcia, DDS, University of Washington
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Actual)
Finalización del estudio (Actual)
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
- STUDY00003980
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
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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