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临床试验/NCT05589493
NCT05589493进行中(未招募)不适用

Hybrid Polyetheretherketone (PEEK)-Acrylic Resin Prostheses and the All-on-4 Concept for Full-Arch Rehabilitation - Routine Group

Malo Clinic2 个研究点 分布在 1 个国家目标入组 39 人开始时间: 2017年11月13日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
39
试验地点
2
主要终点
Survival of the prosthesis

研究概览

简要总结

The goal of this observational study is to evaluate the outcome of a Poly-ether-ether-ketone - acrylic resin prosthesis for full-arch rehabilitation of the atrophic maxillae through the All-on-4 concept after five years of follow-up. The main question it aims to answer is:

  • What is the survival outcome of the full-arch implant-supported Poly-ether-ether-ketone - acrylic resin prosthesis? The participants already rehabilitated with dental implants will receive a Poly-ether-ehter-ketone prosthesis as a definitive prosthesis.

详细描述

Following the learning generated during a development study with implant supported fixed prostheses using polyetheretherketone (PEEK) material, it is necessary to evaluate the outcome of implant supported fixed prosthetic rehabilitations using PEEK material in a routine scenario, following optimized laboratory and treatment protocol.

The study design will be a prospective single cohort to evaluate the long term outcome of fixed prosthetic implant supported rehabilitations. The cohort will be evaluated at 6 months, 12 months and annually thereafter until 5 years of follow-up. At each follow-up assessments multiple evaluaitons will be performed to assess the overall outcome of the restorations.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Patients rehabilitated with immediate function implants for complete edentulous arches through the All-on-4 Concept.
  • Patients in need of definitive implant-supported restorations.
  • Written informed consent from each patient to participate in the study.

排除标准

  • Hindrance to provide written informed consent. (A patient cannot participate if no written consent is given)

结局指标

主要结局

Survival of the prosthesis

时间窗: 5 years

Evaluation of the survival for the PEEK-acrylic resin implant-supported prosthesis; nominal (survival,failure)

次要结局

  • Overall classification from KOL(5 years)
  • Manufacture issues(5 years)
  • Speech(5 years)
  • Survival of the implants(5 years)
  • Overall chewing feeling(5 years)
  • Oral Health Impact Profile OHIP-14(5 years)
  • Veneer adhesion(5 years)
  • Incidence of mechanical complications(5 years)
  • Denture staining(5 years)
  • In mouth comfort(5 years)
  • Hygiene around the implants(5 years)
  • Incidence of biological complications(5 years)
  • Handling of material compared to metal(5 years)
  • Hygiene - how much plaque/calculus adheres to the prosthesis(5 years)
  • Marginal bone resorption(5 years)
  • Patient tissue reaction(5 years)
  • Framework integrity(5 years)
  • Fit(5 years)
  • Aesthetics(5 years)

研究者

发起方
Malo Clinic
申办方类型
Other
责任方
Sponsor

研究点 (2)

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