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临床试验/NCT06759246
NCT06759246已完成不适用

Short Implant Placement for Single-Tooth Rehabilitation in the Atrophic Posterior Maxilla

University of Bari Aldo Moro2 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2014年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
150
试验地点
2
主要终点
Clinical outcome

研究概览

简要总结

This study aims to evaluate the clinical and radiological outcomes of short implants in the rehabilitation of single-tooth edentulism in the posterior maxilla. By assessing these outcomes, the research seeks to determine the effectiveness and long-term viability of short implants as a minimally invasive solution, particularly in cases where bone height is limited.

详细描述

The present municentric retrospective study was conducted following the STROBE statement recommendations for observational studies and in compliance to the principles of the Declaration of Helsinki on clinical research involving human subjects.The study aims to evaluate short implants placed over the past 15 years by three experienced clinicians, assessing their survival and clinical success. Specifically, the study collects clinical data such as probing depth, the presence or absence of peri-implantitis, and radiological findings.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Screening
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

  • Good health status according to the classification system of the American Society of Anesthesiology (ASA), and patients were required to be 18 years of age or older.
  • No general medical condition that would contraindicate implant therapy.
  • No active periodontal disease, defined as a periodontal probing depth of less than 4 mm, or previously treated periodontitis.
  • Good oral hygiene, with a full-mouth plaque index of less than 25%.
  • Adequate control of inflammation, with a full-mouth bleeding on probing (BOP) of less than 25%.

排除标准

  • Smoking more than 15 cigarettes per day
  • Presence of untreated periodontal disease
  • Pregnancy or breastfeeding at the time of enrollment
  • Active infections
  • Less than 2 mm of keratinized mucosal tissue.

结局指标

主要结局

Clinical outcome

时间窗: 2 years

Survival rate: A statistical analysis will be conducted to evaluate the implant survival rate at three specific time points: T1 (3 months), T2 (6 months), and T3 (2 years).

次要结局

  • Rx outcome(2 years)

研究者

发起方
University of Bari Aldo Moro
申办方类型
Other
责任方
Principal Investigator
主要研究者

Giuseppe D'Albis

Dr. D'Albis Giuseppe

University of Bari Aldo Moro

研究点 (2)

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