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临床试验/IRCT201204302016N5
IRCT201204302016N5已完成未知

Comparison of anesthetic efficacy of 4% articaine and 2% Lidocaine for maxillary Buccal infiltration in patients with irreversible pulpitis. a randomized double- blined clinical trial

Vice chancellor for research; Kerman University of Medical Sciences0 个研究点目标入组 50 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
50

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 80 years(—)
性别
All

入选标准

  • The exclusion criteria were the presence of systemic disorders; a sensitivity to articaine 4%with 1:100000 epinephrine and lidocaine2% with 1:80,000 epinephrine; the presence of widening of the periodontal ligament space; the presence of a periapical radiolucency; lactation; pregnancy. Inclusion criteria included healthy patients having a first maxillary molar tooth with irreversible pulpitis and normal periapical radiographic appearance, whit out spontaneously pain that to be needed emergency treatment.

排除标准

  • 未提供

研究者

发起方
Vice chancellor for research; Kerman University of Medical Sciences

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