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临床试验/NCT07040124
NCT07040124已完成不适用

Assessment of Efficacy of Prebent Titanium Mesh Versus Customized Poly-ether Ether Ketone Mesh for Three Dimensional Augmentation in Deficient Maxillary Ridge. a Randomized Controlled Clinical Trial.

Basma Alsheikh1 个研究点 分布在 1 个国家目标入组 8 人开始时间: 2020年10月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
8
试验地点
1
主要终点
horizontal bone gain

研究概览

简要总结

In conclusion, the choice between titanium and PEEK meshes should consider patient-specific factors, clinical requirements, and surgeon expertise. The PEEK mesh, with its patient customized design enabled by CAD/CAM technology, offers significant advantages, including greater gained bone volume and reduced operative time. Its tailored fabrication ensures precise adaptation to the patient's anatomy, effectively maintaining the space required for optimal bone formation. The integration of such advanced technologies in regenerative procedures represents a significant step forward in achieving predictable outcomes and enhancing patient care. However, continued innovation and evaluation are crucial to refine these approaches and expand their applicability in oral rehabilitation

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Adult patient of both sexes presenting with partially edentulous maxillary ridge with horizontal bone defect.
  • •The horizontal ridge dimension measured 2mm below the alveolar crest should range from 2-5 mm.
  • •No local pathosis that may interfere with bone healing.
  • •Good oral hygiene.
  • •Age between 20-65 years old.

排除标准

  • •Patient taking any medication that may interfere with normal bone physiology or impair bone healing.
  • •All patients suffering from any systemic disease that may affect bone healing.
  • •Heavy smokers (more than 10 cigarette per day)
  • •Patients with parafunctional habits such as bruxism and clenching
  • •Poor interest and cooperation from the patient.
  • •Patients that have undergone any horizontal augmentation procedure at the site of interest

研究组 & 干预措施

prebent titanium mesh

Active Comparator

participants receive alveolar ridge augmentation using pre-bent titanium mesh

干预措施: ti mesh (Procedure)

3d peek mesh

Active Comparator

participants receive maxillary ridge augmentation using 3d milled peek mesh

干预措施: 3d peek mesh (Procedure)

结局指标

主要结局

horizontal bone gain

时间窗: 6 months

cbct analysis for bone gain

次要结局

未报告次要终点

研究者

发起方
Basma Alsheikh
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Basma Alsheikh

assistant lecturer

British University In Egypt

研究点 (1)

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