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临床试验/NCT07268456
NCT07268456已完成不适用

Volumetric Bone Reconstruction of Complex Alveolar Ridge Defects Using CAD/CAM-Customized Titanium Meshes: A Retrospective Study

TC Erciyes University1 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2025年2月6日最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
15
试验地点
1
主要终点
planned bone volume

研究概览

简要总结

Brief introduction: After tooth extraction, alveolar defects may hinder implant placement. Digital imaging and CAD/CAM advances allow creation of patient-specific titanium meshes for effective bone augmentation.

Objective: This study aimed to evaluate the clinical effectiveness of customized titanium meshes produced using computer-aided design and manufacturing (CAD/CAM) technologies in the horizontal and vertical augmentation of complex alveolar ridge defects prior to implant placement.

详细描述

Implant dentistry is a recognized and dependable method for restoring functionality and aesthetics in individuals with partial or total tooth loss. Following tooth loss or extraction, the alveolar bone undergoes gradual resorption and atrophy. This process generally commences with a notable horizontal decrease in ridge width over the initial six months, succeeded by vertical bone loss over time. Consequently, patients often have horizontal, vertical, or mixed alveolar defects that hinder later implant implantation.

Attaining sufficient bone volume before implant surgery is essential for enduring functional and aesthetic results. Horizontal and vertical bone augmentation procedures have demonstrated efficacy in enhancing alveolar ridge dimensions and facilitating the outcome of implant therapy. Among them, guided bone regeneration (GBR) is one of the most extensively utilized and evidence-based techniques, due to its reliability and capacity to facilitate new bone creation. Guided Bone Regeneration (GBR) employs resorbable or non-resorbable membranes alongside bone graft materials to safeguard the clot, prevent soft tissue encroachment, and promote osteogenesis within the defect.

Notwithstanding its prevalent application, the choice of membrane type continues to be a subject of contention. Resorbable membranes are manageable; nonetheless, they may exhibit inadequate mechanical stability, which could jeopardize the volume of regenerated bone. Conversely, non-resorbable membranes, especially titanium-reinforced polytetrafluoroethylene (PTFE) membranes, demonstrate enhanced space maintenance and they are considered more reliable for addressing extensive flaws.

In the late 1960s, titanium meshes were offered as a substitute for conventional membranes. These meshes provide improved stiffness and biocompatibility, rendering them appropriate for intricate ridge augmentation scenarios. Nevertheless, conventional titanium meshes require manual adjustment during surgery, potentially prolonging operative time and resulting in problems such as soft tissue dehiscence, mesh exposure, and postoperative infection due to inadequate fit.

Recent advancements in digital imaging and CAD/CAM technology have facilitated the creation of patient-specific titanium meshes, tailored according to preoperative cone beam computed tomography (CBCT) data. These bespoke meshes provide enhanced anatomical conformity, decrease intraoperative handling, reduce surgery duration, and mitigate problems linked to conventional meshes. Their smooth surface and exact fit to the bone defects correlate with reduced exposure rates and improved surgical results. However, limited studies have quantitatively assessed the volumetric outcomes of CAD/CAM-fabricated meshes using standardized CBCT-based protocols.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Retrospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Comprised the presence of alveolar bone defects involving both vertical and horizontal components in edentulous regions of the maxilla.
  • Comprised the presence of alveolar bone defects involving both vertical and horizontal components in edentulous regions of the mandible.

排除标准

  • uncontrolled systemic disease,
  • poor oral hygiene,
  • active oral infections,
  • autoimmune or inflammatory oral diseases,
  • pregnancy,
  • histories of head and neck radiotherapy, chemotherapy in the past six months,
  • corticosteroid use,
  • or smoking more than 10 cigarettes per day.

结局指标

主要结局

planned bone volume

时间窗: beginning to 4-6 months

planned bone volume when mesh was designed

planned horizontal width

时间窗: beginning to 4-6 months

planned horizontal width when mesh was designed

planned vertical height

时间窗: beginning to 4-6 months

planned vertical height when mesh was designed

regenerated bone volume

时间窗: beginning to 4-6 months

regenerated bone volume when mesh was applied to the patient

regenerated horizontal width

时间窗: beginning to 4-6 months

regenerated horizontal width when mesh was applied to the patient

regenerated vertical height

时间窗: beginning to 4-6 months

regenerated vertical height when mesh was applied to the patient

次要结局

  • mesh exposure rate(begining to 4-6 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Duygu Kilic

Principal Investigator

TC Erciyes University

研究点 (1)

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