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临床试验/IRCT20211230053569N1
IRCT20211230053569N1已完成1 期

Comparison of anesthetic efficacy of articaine with lidocaine as an inferior nerve blocking agent in subjects with symptomatic irreversible pulpitis

Riphah International University0 个研究点目标入组 152 人开始时间: 待定最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
152

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
26 years 至 35 years(—)
性别
All

入选标准

  • Subjects of both genders (males and females), in good health, with no systemic disease that will interfere with the action of any of the anesthetic solutions being used, aged between 26 – 35 years
  • Mandibular posterior teeth requiring endodontic treatment due to symptomatic irreversible pulpitis
  • There should have been no previous attempts of endodontic therapy on that tooth
  • Positive pulp sensibility testing (cold testing)

排除标准

  • Patients who have known allergy to amides
  • Patients taking any medication that will alter their perception of pain
  • Patients who are suffering from any heart disease, diabetes mellitus
  • Female patients who are pregnant

研究者

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