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临床试验/IRCT20230301057581N1
IRCT20230301057581N1招募中未知

Comparison of the success rate of two anesthetic techniques using lidocain 2% in mandibular first premolars with symptomatic irreversible pulpitis

Tabriz University of Medical Sciences0 个研究点目标入组 90 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
招募中
入组人数
90

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 65 years(—)
性别
All

入选标准

  • No systemic diseases
  • No facial paresthesia
  • Not taking drugs that interfere with anesthesia
  • Absence of periodontal problems in the second premolar region of the mandible

排除标准

  • Patients with congenital anomalies and structural defects in premolar teeth
  • Patients undergoing radiotherapy or chemotherapy
  • Patients with an allergy to anesthetics
  • Smoking patients

研究者

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