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临床试验/NCT06262841
NCT06262841已完成不适用

Comparative Evaluation of Morbidity and Alveolar Bone Healing After Surgical Extraction of Impacted Lower Third Molar Teeth Using Piezosurgery and Conventional Instruments: A Split-Mouth Clinical Study

Ankara University2 个研究点 分布在 2 个国家目标入组 21 人开始时间: 2022年11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
21
试验地点
2
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.

详细描述

The aim of our study is to comparatively evaluate the duration of the operation and the pain, trismus, edema and healing of the alveolar bone that occur after tooth extraction in surgical extractions of impacted lower third molar teeth using piezosurgery and traditional rotary instruments.

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

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

Conventional group

Active Comparator

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

Intervention: Device: Conventional burs

干预措施: Conventional burs (Device)

Piezosurgery group

Experimental

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

Intervention: Device: Piezosurgery

干预措施: Piezosurgery (Device)

结局指标

主要结局

Change in Oral Health-related Quality of Life

时间窗: Time Frame: 14 days

Evaluated by Oral Health Impact Profile-14 questionnaire (OHIP-14). The OHIP-14 scores can range from 0 to 56 and are calculated by summing the ordinal values for the 14 items. The domain scores can range from 0 to 8. Higher OHIP-14 scores indicate worse and lower scores indicate better Oral Health Related Quality of Life.

次要结局

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

研究者

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

Murat Kaan Erdem

Murat Kaan Erdem, Ph.D, DDS. Ankara University Faculty of Dentistry, Department of Oral and Maxillofacial Surgery

Ankara University

研究点 (2)

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