Surface Topography and Color Stability of Implant Supported 3D Printed Provisional Restorations
Ориентир для пациента и семьи
Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- В протоколе указаны: To evaluate the surface topography and color stability of 3D printing provisional material..
- Кому может быть актуально
- Состояния в реестре: DENTAL IMPLANTATION. Базовые параметры: 20 лет — 60 лет · Все.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- Индия
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Официальное название
"Comparative Evaluation of Surface Topography and Color Stability of Implant Supported Provisional Restorations Fabricated Using Two Different 3D Printing Materials in Mandibular Posterior Region: A Randomized Clinical Trial"
Обзор
Patient attending the Outdoor Patient Department of the Department of Prosthodontics at Post Graduate Institute of Dental Sciences, Rohtak will be screened. The screening will include history taking and clinical examination of the partially edentulous patients. Patients will be selected according to the inclusion and exclusion criteria. Single stage endosseous implants will be placed. Two different Biocompatible 3D printed Polymethyl methacrylate resin will constitute two groups, Group A and Group B. 3D printed provisional poly methyl methacrylate resin crowns will be fabricated with Group- A and Group-B material followed by evaluation of surface topography and color stability after intraoral use.
Подробное описание
Title: "Comparative Evaluation of Surface Topography and Color Stability of Implant Supported Provisional Restorations Fabricated using Two Different 3D Printing Materials in Mandibular Posterior Region: A Randomized Clinical Trial".
Rationale: The study needs to verify the surface topography and color stability of implant supported provisional restorations fabricated using two different 3D printing materials in mandibular posterior region.
Aim and objectives: To evaluate the surface topography and color stability of implant supported provisional restorations fabricated using two different 3D printing materials in mandibular posterior region.
Setting: Department of Prosthodontics and Crown \& Bridge, PGIDS Rohtak. Study Design: Randomised clinical trial. Population/Participants: Provisional restoration will be fabricated using two different 3D printing materials.
Sample Size: Total of 24 samples will be prepared (n=12 samples per test group).
Methodology: This is an in-vivo study and will be carried out in the Department of Prosthodontics and Crown \& Bridge, Post Graduate Institute of Dental Sciences, Rohtak with the purpose to evaluate the surface topography and color stability of implant supported provisional restorations fabricated using two different 3D printing materials in mandibular posterior region.
Outcome Measures: Measuring the surface topography using profilometer and color stability using spectrophotometer.
Statistical Analysis: Data obtained would be compiled on MS Office Excel Sheet (v 2010) and will be subjected to statistical analysis using statistical package for social sciences (SPSS v 21.0, IBM). Intergroup and intragroup comparisons will be done according to distribution of data.
Вмешательства
- Процедура To evaluate the surface topography and color stability of 3D printing provisional material.
Subjects with single stage implant placement followed by early non-functional loading with implant supported provisional restorations fabricated using 3D printing provisional material.
Первичные конечные точки
- Surface topography of provisional restorations. [Срок оценки: 2 years]
- Color stability of provisional restorations [Срок оценки: 2 years]
Критерии участия
Критерии включения
- Subjects consented to participate in the study.
- Subjects with maintainable oral hygiene.
- Subjects with adequate edentulous space at the prospective implant site.
- Subjects with availability of adequate quantity and quality of bone.
Критерии исключения
- Subject with presence of infection around proposed site of implant placement.
- Subjects with any condition that would interfere with the soft tissue and bone healing.
- Subjects in which surgical procedure is contraindicated for any reasons.
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Да
Дизайн исследования
- Распределение
- Рандомизированное
- Модель
- Параллельные группы
- Маскирование
- Четверное слепое
- Основная цель
- Лечение
Центры проведения
Индия · 1 центр
- PGIDS — Rohtak
Идентификаторы
NCT: NCT06947070 · Dr. Kritika Diwan