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临床试验/IRCT20210515051306N1
IRCT20210515051306N1招募中未知

Comparative evaluation of anesthetic efficacy of 1.8 mL articaine, 1.8 mL and 3.6 mL of lidocaine for mental nerve block in mandibular premolar with irreversible pulpitis

Rafsanjan University of Medical Sciences0 个研究点目标入组 165 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
165

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 60 years(—)
性别
All

入选标准

  • Healthy adult patients 18–60 years old
  • Having a mandibular premolar tooth with symptomatic irreversible pulpitis
  • Normal periapical radiographic appearance

排除标准

  • History of sensitivity to 4%articaine or epinephrine
  • Systemic diseases
  • Pregnancy or breastfeeding
  • Any type of medication that could potentially interact with the anesthetic solution
  • Spontaneous pain
  • Periodontal disease or unable to get restoration
  • Having pain killer late 12 hours

研究者

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