Evaluating The Clinical Success And Patient Satisfaction of Digital, Conventional, And Biomimetic Approaches For Restoring Endodontically Treated Teeth: Randomized Controlled Trial.
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 42
- 试验地点
- 2
- 主要终点
- Clinical success and survival of restoration
研究概览
简要总结
Endocrowns are preferred over the post-retained crown, especially at a young age for many reasons; they allow better gingival health and care due to placement of the supragingival margin, have greater fracture resistance limiting the risk for root fracture, thus improving the long-term prognosis of ETMs and has a superior ability to restore ETMs with short crowns, calcified root canals, and thin roots. Furthermore, using CAD/CAM technology facilitates Endocrowns preparation making it simpler with less invasive techniques that can be prepared, fabricated, and cemented in a single visit. The high demand for permanent, esthetic, and conservative restorations has directed clinicians to restore permanent ETMs at a young age with Endo crowns as final coronal restorations.
In addition, Biomimetic dentistry leverages modern materials to replicate the biological and mechanical functions of natural teeth, presenting a distinct approach that minimizes the need for extensive tooth reduction and post-placement, particularly advantageous for endodontically treated teeth. Utilizing fiber-reinforced composites, this technique aims to strengthen the dentin-resin bond and evenly distribute occlusal forces across the restoration. By closely adhering to the intact tooth's natural contours and functionality, biomimetic restorations not only preserve more of the natural tooth structure but also reduce stress and strain within the restored tooth. This approach enhances longevity and minimizes the risk of bond failure, with any necessary repairs being straightforward and contributing to the restoration's sustainability. This study explores the application of fiber-reinforced composites within a biomimetic framework for restoring endodontically treated teeth, aiming to achieve durable and biologically compatible outcomes.
详细描述
This randomized controlled trial study will evaluate the clinical success of digital, conventional, and biomimetic techniques in restoring endodontically treated mandibular first permanent molars.
Research question:
Are Lithium Disilicate Endo-Crowns, EverX Posterior with Vita Endo-Crowns, and EverX Posterior with Bulk-Fill Resin Restorations Clinically Successful for Restoring Endodontically Treated Mandibular First Permanent Molars?
PICOS:
P: Patients aged ≥15 years with endodontically treated mandibular first permanent molars.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Triple (Participant, Care Provider, Outcomes Assessor)
盲法说明
The child participants and the legal guardian of each participating child and the statistician were blinded.
入排标准
- 年龄范围
- 15 Years 至 —(Child, Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Endodontically-treated molar tooth with significant loss of tooth structure (both marginal ridges lost) requiring cuspal coverage.
- •Patients aged ≥15 years.
- •Controlled dental disease - no active caries or periodontal diseases
- •Patients will be available to be clinically reviewed up to 1 year
排除标准
- •Patients with poor oral hygiene.
- •Teeth with extensive cracks or fractures.
- •Deep subgingival margins (>0.5mm subgingival).
- •Non-restorable teeth.
- •Non-functional teeth (no opposing dentition).
- •Pocket probing depth > 3mm.
- •Mobility.
- •Patients with bruxism.
结局指标
主要结局
Clinical success and survival of restoration
时间窗: 12 months
* Clinical success will be evaluated using (a modified version of the United States Public Health Service (USPHS) criteria which involves the assessment of margins, anatomic form, surface texture, and shade match. (Rate: Alfa, Bravo, Charlie) * Each parameter will be assessed using visual and tactile observations (probe, mirror, and dental floss). * Treatment will be considered a failure if the restoration had to be remade for any reason including debonding, fracture, or poor appearance, during the 12-month observation period.
次要结局
- The radiographic assessment(12 months)
- Patient-centred outcomes to the restoration(12 months)
