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临床试验/NCT05545553
NCT05545553已完成不适用

A Randomized Split Mouth Clinical Trial Comparing Piezosurgery and Conventional Rotary Instruments on Impacted Third Molar Surgery

Marmara University1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2021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
入组人数
20
试验地点
1
主要终点
Change in Oral Health-related Quality of Life

研究概览

简要总结

The aim of this study is to compare piezosurgery and conventional surgery in impacted third molar surgery and to determine its effect on postoperative outcomes and quality of life.

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 (Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Aged 18-35
  • •Symmetrical Class 2 Position B according to Winter and Pell-gregory classification
  • •Asymptomatic lower third molar tooth with the same difficulty according to the Yuasa difficulty index

排除标准

  • •Individuals who had systemic disease affecting bone or soft tissue metabolism
  • •Smokers (more than 10 cigarettes a day
  • •Alcohol dependent
  • •Systemic disease affecting bone or soft tissue metabolism
  • •Acute pericoronitis or acute periodontal disease at the time of operation, and used antibiotics due to acute infection

研究组 & 干预措施

Piezosurgery group

Experimental

In the experimental group, a piezosurgery device was used to remove the bone surrounding the impacted third molar.

干预措施: Piezosurgery (Device)

Conventional group

Active Comparator

In the control group, conventional burs were used to remove the bone surrounding the impacted third molar.

干预措施: Conventional burs (Device)

结局指标

主要结局

Change in Oral Health-related Quality of Life

时间窗: 14 days

Evaluated by OHIP-14

次要结局

  • Change in Mouth opening(7 days)
  • Operation time(Intraoperative)
  • Change in pain(7 days)
  • Change in facial swelling(7 days)

研究者

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

Ferit Bayram

Assistant Professor

Marmara University

研究点 (1)

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