Aesthetic Evaluation of Two Piece 3mm Implants for Single Tooth Replacement of Maxillary Laterals and Mandibular Incisors
Descripción general del estudio
Estado
Condiciones
Descripción detallada
PURPOSE OF THE STUDY:
The purpose of this research study is to examine the aesthetics (the appearance of the implanted tooth and gums) as well as the soft tissue loss over a three-year period. This study involves replacing a missing small front tooth with a dental implant, abutment, and crown. A titanium dental implant acts as the replacement for a tooth root. An abutment is made of titanium which is either gold or silver in color and cannot be seen; but may affect the way the gum looks. An abutment is the component that attaches the crown to the implant post. A crown (which acts as the tooth replacement) is made of metal and/or porcelain and attaches over the abutment.
The dental implant and the abutments used in this study have been approved by Health Canada and the U.S. Food and Drug Administration (FDA) for the use of replacing the small teeth in the front of the mouth.
The abutment is made in two colors (either gold or silver) and you cannot choose. For each subject this is decided by chance. You will have an equal chance of getting a gold or silver-colored attachment. You will know which color the abutment will be once you have consented to be in the study and registered. You will know the color of the abutment before the implant is placed. The abutment is covered by the crown.
You will be in this study for about three years. There will be approximately 60 subjects who will participate in this study in different centres, in Canada and the USA.
Tipo de estudio
Inscripción (Anticipado)
Contactos y Ubicaciones
Ubicaciones de estudio
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Ontario
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Toronto, Ontario, Canadá, M5R 3K4
- Dr. Suzanne Caudry PhD DDS MSc Perio Implant Dentistry and Periodontics
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Método de muestreo
Población de estudio
Descripción
Inclusion Criteria:
- Capacity to provide written informed consent to participate in the study.
- 18 years or older
Site requirements:
Missing one or both maxillary lateral incisors (if missing both, then both sites must be used in the study) or Single missing mandibular incisor or Two missing mandibular incisors, not adjacent to one another (both sites must be used in the study) Aside from the missing teeth specified above, all other teeth in the sextant must be present.
A minimum of premolar occlusion is required. A minimum mesio-distal and buccal-lingual distance of 5mm is required
Exclusion Criteria:
- Rampant caries or unstable periodontal disease of the remaining dentition.
- Any systemic or local disease or condition that may compromise post-operative healing.
- Long-term use of systemic corticosteroids or other medications that may compromise post-operative healing.
- Present alcohol and/or drug abuse.
- Unable or unwilling to return for follow-up exams over a 3 year period.
- Pregnancy or lactation at time of enrollment.
- Smokers will be excluded from the subject pool.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
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Recession
Periodo de tiempo: every 12 months for 3 years
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The Astra Tech 3.0 mm 2 piece implant can be placed and restored in a 5 mm or greater bone space for a mandibular incisor or maxillary lateral incisor site (minimum 5 mm mesio-distal [side to side] bone width and 5mm bucco-lingual [front to back] bone width) without exhibiting recession of the soft tissue (gingival margin or the interproximal papillae).
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every 12 months for 3 years
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
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Esthetic parameter Scores
Periodo de tiempo: every 12 months up to three years
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Esthetic parameter scores will be higher when the Atlantis Gold Hue titanium abutment is used in comparison to the Atlantis titanium abutment.
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every 12 months up to three years
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Dr. Suzanne D Caudry, DDS PhD, Implant Dentistry and Periodontics
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización primaria (Anticipado)
Finalización del estudio (Anticipado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
Actualizaciones de registros de estudio
Última actualización publicada (Estimar)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Otros números de identificación del estudio
- WIRB® Protocol #20101573
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