Clinician- vs. Patient-Reported Esthetic Outcomes After Coronally Advanced Flap
Comparison of Clinician- and Patient-Reported Esthetic Outcomes Following Coronally Advanced Flap Procedures for the Treatment of Gingival Recession
This study aims to evaluate the relationship between clinician-assessed esthetic outcomes, measured using the Root Coverage Esthetic Score, and patient-reported esthetic outcomes, recorded on a Visual Analog Scale, at 6 months following the treatment of Cairo Recession Type 1 and Type 2 gingival recessions with a coronally advanced flap, combined with a connective tissue graft where clinically indicated.
Descripción general del estudio
Estado
Intervención / Tratamiento
Descripción detallada
In this prospective clinical study, patients who apply to our clinic due to the esthetic complaint or dentin sensitivity will be included. After initial periodontal treatment, patients who meet the criteria will have a coronally positioned flap applied under local anesthesia. In areas where the keratinized tissue width is 2 mm or more and the keratinized tissue thickness is more than 1 mm, a coronally positioned flap will be applied alone. In areas where the keratinized tissue width is less than 2 mm and/or the keratinized tissue thickness is 1 mm or less, a connective tissue graft will be applied in addition to the coronally positioned flap. Clinician and patient results will be compared in the esthetic evaluations to be performed six months after the surgical procedure.
Tipo de estudio
Inscripción (Estimado)
Fase
- No aplica
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Ezgi Gürbüz, DDS PhD
- Número de teléfono: +905557411860
- Correo electrónico: ezgi.dogan@ksbu.edu.tr
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Systemically healthy individuals
- Individuals over 18 years of age
- Individuals who do not smoke and/or consume alcohol
- Individuals without active periodontitis
- Individuals with full-mouth plaque and bleeding scores of less than 15%
- Presence of single or multiple gingival recessions in the maxilla or mandible
- The affected tooth must be single-rooted
- Presence of Cairo classification Type 1 or Type 2 gingival recession on the buccal surface of the tooth
- A recession depth of at least 2 mm
Exclusion Criteria:
- Individuals with uncontrolled systemic diseases
- Women who are pregnant or breastfeeding
- Individuals who smoke and/or consume alcohol
- Individuals with active periodontitis
- Cases involving tooth rotation or malposition
- Individuals currently undergoing orthodontic treatment
- Gingival recessions associated with teeth that have undergone endodontic treatment or require restorations
- Teeth with dental caries
- Gingival recessions with non-carious cervical lesions that have a horizontal depth (step depth) greater than 1 mm
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Coronally advanced flap procedure
Coronally advanced flap procedure for Cairo type 1 or 2 gingival recession sites |
Patients will have a coronally positioned flap applied under local anesthesia. In areas where the keratinized tissue width is 2 mm or more and the keratinized tissue thickness is more than 1 mm, a coronally positioned flap will be applied alone. In areas where the keratinized tissue width is less than 2 mm and/or the keratinized tissue thickness is 1 mm or less, a connective tissue graft will be applied in addition to the coronally positioned flap. |
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Root Coverage Esthetic Score
Periodo de tiempo: Post-operative 6th month
|
The Root Coverage Esthetic Score evaluates five variables 6 months following surgery (gingival margin, marginal tissue contour, soft tissue texture, mucogingival junction alignment, and gingival color). |
Post-operative 6th month
|
|
Patient-reported esthetic outcome
Periodo de tiempo: Post-operative 6th month
|
Patient-reported esthetic outcome will be measured by the Visual Analog Scale (0 representing the minimum value, and 100 maximum value). |
Post-operative 6th month
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Recession depth
Periodo de tiempo: Pre-operative and post-operative 6th month
|
The distance between gingival margin and cemento-enamel junction |
Pre-operative and post-operative 6th month
|
|
Keratinized tissue width
Periodo de tiempo: Pre-operative and post-operative 6th month
|
The distance between gingival margin and mucogingival junction |
Pre-operative and post-operative 6th month
|
|
Keratinized tissue thickness
Periodo de tiempo: Pre-operative and post-operative 6th month
|
The thickness measured 1.5 mm apical to the gingival margin |
Pre-operative and post-operative 6th month
|
|
Vestibular depth
Periodo de tiempo: Pre-operative and post-operative 6th month
|
The distance between the gingival margin and the greatest concavity at the mucosal fold |
Pre-operative and post-operative 6th month
|
|
Mean root coverage
Periodo de tiempo: Post-operative 6th month
|
([Pre-operative Recession Depth - Post-operative Recession Depth] / Pre-operative Recession Depth) × 100 |
Post-operative 6th month
|
|
Linear dimension change
Periodo de tiempo: Post-operative 6th month
|
The changes in the horizontal plane measured by superimposition of the STL files |
Post-operative 6th month
|
Colaboradores e Investigadores
Patrocinador
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
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- KSBU002
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.
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