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临床试验/IRCT20210515051306N3
IRCT20210515051306N3尚未招募Unknown

Investigating the success rate of infiltrating anesthetic injection of 1.8 ml of Articaine, injection of 1.8 ml of Articaine as mental block and injection of 1.8 ml of Lidocaine as mental block in mandibular incisor teeth with irreversible pulpitis: A randomized clinical trial

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
Unknown
状态
尚未招募
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 incisor tooth with symptomatic irreversible pulpitis
  • Normal periapical radiographic appearance

排除标准

  • Patients under age of 18 and over the age of 60 years
  • American Society of Anesthesiologists (ASA) III,IV patients
  • Pregnancy or breasfeeding
  • 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
  • History of sensititivity to 4% articaine, 2% lidocaine or epinephrine
  • Widening PDL
  • Radiolucency in radiography
  • Incisor teeth sensitive to percussion

研究者

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