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临床试验/NCT07395167
NCT07395167已完成不适用

Evaluation of Soft Tissue Response and Prosthetic Complication of Three Different Provisional Prosthesis Used for Immediate Load Full Arch Implant Prosthesis. Randomized Control Clinical Trial

Mansoura University1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2024年2月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
10
试验地点
1
主要终点
clinical evaluation of dental implant (bone Level)

研究概览

简要总结

This study aims to evaluate the soft tissue response and prosthetic complications associated with three different types of provisional prostheses used in immediate loading full-arch implant prosthetic treatment. The patients are randomly assigned to the three groups to compare the clinical outcomes and determine which provisional prosthesis provides better soft tissue health and fewer prosthetic complications

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
Single (Participant)

入排标准

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

入选标准

  • - In good general health. Controlled systemic diseases such as well-managed diabetes or hypertension. Good oral hygiene Adequate bone quality and quantity (Type I-III bone, ≥10mm height, ≥6mm width).

排除标准

  • Uncontrolled systemic diseases Bone insufficiency Active infection or periodontal disease. Pregnancy. Heavy smokers (>10 cigarettes/day). History of previous implant failure in the same site. Immunocompromised patients (e.g., HIV, recent radiation therapy

研究组 & 干预措施

Printed provisional

Experimental

patients received 3D printed provisional full arch prosthesis

干预措施: 3D printed provisional full arch prosthesis (Device)

Bar reinforced provisional

Experimental

patients received Bar reinforced 3D printed provisional full arch prosthesis.

干预措施: Bar reinforced 3D printed provisional full arch prosthesis (Device)

Milled provisional

Experimental

patient received Milled PMMA provisional full arch prosthesis.

干预措施: Milled PMMA provisional full arch prosthesis (Device)

结局指标

主要结局

clinical evaluation of dental implant (bone Level)

时间窗: 3 months

Evaluation included alveolar bone level around implant which is evaluated using periapical x-rays comparing T0 (at implant insertion) to T1 ( at one and half month) and T2 (at three months ) measuring amount of bone resorption around implant

次要结局

  • modified plaque index(3 months)
  • the Modified Gingival Index (MGI)(3 months)
  • peri-implant probing depth (PD)(3 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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