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临床试验/NCT06342869
NCT06342869已完成不适用

Comparison of the Effects of Lidocaine and Articaine Used for Buccal Infiltration and Supplemental Palatinal Infiltration Anesthesia in Teeth With Irreversible Pulpitis

Akdeniz University2 个研究点 分布在 2 个国家目标入组 80 人开始时间: 2022年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
80
试验地点
2
主要终点
Assessment of complementary palatinal anesthesia with VAS

研究概览

简要总结

Objective: The aim of this study was to compare the effects of articaine or lidocaine in buccal infiltration or palatal infiltration in addition to buccal infiltration in maxillary first or second molars with irreversible pulpitis.

Method: Among the patients who applied to Akdeniz University Faculty of Dentistry Endodontic Clinic for the treatment of maxillary molars with irreversible pulpitis, 80 volunteers who met the criteria were included in the study. Eighty patients were divided into 4 groups (n = 20). 1. group buccal infiltration with 4% articaine containing 1:100,000 epinephrine, 2. group buccal infiltration with 2% lidocaine containing 80,000 epinephrine, 3. group buccal and palatinal infiltration with 4% articaine containing 1:100,000 epinephrine, 4.group buccal and palatinal infiltration with 2% lidocaine containing 80.000 epinephrine. Pain during the endodontic procedure was determined and recorded according to the Heft Parker visual analog scale.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • The patient must be a healthy individual between the ages of 18 and 65 who is classified as ASA I and II.
  • No allergy to local anesthetic substances to be used in the study
  • Upper maxillary molars with irreversible pulpitis whose vitality has been proven by pulp tests, with no radiolucency at the root tip
  • Not having used any painkillers, antibiotics, antidepressants and sedative drugs in the last 12 hours
  • Being capable of understanding the Pain scale

排除标准

  • Allergy to local anesthetics
  • Failure to respond to the cold test and electric pulp test performed on the relevant tooth
  • Radiolucent lesion in the apical part of the relevant tooth on periapical radiography
  • No vital tissue is encountered when the pulp chamber is opened

结局指标

主要结局

Assessment of complementary palatinal anesthesia with VAS

时间窗: 10 minutes after anesthesia is performed

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Damla Kırıcı

associate professor

Akdeniz University

研究点 (2)

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