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临床试验/IRCT20200406046966N1
IRCT20200406046966N1已完成3 期

Evaluation of patient's sedation and surgeon's satisfaction by applying the combination of Dexmedetomidine and Lidocaine during wisdom tooth surgery

Esfahan University of Medical Sciences0 个研究点目标入组 26 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
入组人数
26

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 years 至 30 years(—)
性别
All

入选标准

  • According to the ASA physical status classification system, patient should be ASA I or ASA II (normal healthy patient or patient with mild systemic disease).
  • Patient with informed consent.
  • Patient's age should be between 18-30 years.
  • Patients should have two wisdom teeth (classified in the same class by Pell & Gregory; mesioangular impaction, level B, class 1 or 2), which are similar in terms of surgical severity;
  • No general contraindications (in these patients use of dexmedetomidine is contraindicated: patients with low blood pressure, bradycardia, sinus disorder, unstable high blood pressure, arousability, tachyphylaxis and liver disorders.)
  • No lesions and malignancies at the surgical site;
  • No smoking.

排除标准

  • Patient with wisdom tooth surgery on one side;
  • Occurring medical problems during surgery;
  • Patient who needs more than one cartridge injection;
  • Surgery lasting more than 20 minutes.

研究者

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