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临床试验/NCT06971653
NCT06971653已完成不适用

Piezoelectric Versus Conventional Surgical Approaches in Third Molar Removal: A Focus on Pain, Comfort, and Patient Satisfaction

Ege University0 个研究点目标入组 60 人开始时间: 2012年1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
60
主要终点
Postoperative pain with Routine and Piezoelectric Surgery

研究概览

简要总结

The purpose of this study is to compare the effects of piezoelectric surgery on postoperative pain, comfort and patient satisfaction with conventional bur method applied in surgical extraction of impacted mandibular third molars.

The main question it aims to answer is:

Is piezoelectric surgery effective on reducing pain and increasing comfort and patient satisfaction in impacted third molar surgery? Pain levels were assessed using the Visual Analog Scale (VAS), and patient satisfaction was measured with functional evaluations conducted on the 1st, 3rd, and 7th postoperative days.

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
20 Years 至 40 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Patients with mesioangular, distoangular, vertical or horizontal, fully impacted and fully bone retained impacted lower wisdom teeth
  • •Patients without any systemic disease
  • •Patients who have been informed about the duration, purpose and requirements of the study and who have signed the informed consent form voluntarily.

排除标准

  • •Patients with any systemic contraindication, infection in the area of the tooth to be extracted, anamnesis of sensitivity to paracetamol derivatives or aspirin, pregnant or breastfeeding patients, and patients using antibiotics or anti-inflammatory drugs in the last 3 weeks
  • •In addition, smokers or alcohol addicts were not included in the study.

研究组 & 干预措施

30 patients in the piezoelectric surgery group

Experimental

干预措施: piezoelectric surgery (Procedure)

30 patients in the conventional surgery group

Experimental

干预措施: conventional surgery (Procedure)

结局指标

主要结局

Postoperative pain with Routine and Piezoelectric Surgery

时间窗: The postoperative outcomes including pain are clinically assessed at different-time intervals (6th and 12th hours after the operation, 1st, 2nd, 3rd and 7th days after the operation).

The primary outcome measure is postoperative pain with Routine and Piezoelectric Surgery in bilateral impacted third molar. Postoperative pain is assessed using the numbered and visual pain scale. Patients are asked to mark the pain they felt on the scale days after the operation.

次要结局

  • Chewing, Swallowing and Speaking Functions with Routine and Piezoelectric Surgery(The postoperative outcomes including chewing, swallowing and speaking are clinically assessed at different-time intervals (1st, 2nd, 3rd, 4th, 5th, 6th and 7th days postoperative days).)

研究者

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

Mert Zeytinoğlu

Assoc. Prof. Dr.

Ege University

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