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临床试验/TCTR20220715003
TCTR20220715003Unknown4 期

Efficacy of single buccal infiltration of 4% articaine with 1:100,000 epinephrine and 2% mepivacaine with 1:100,000 epinephrine during maxillary premolar teeth extraction: a Double-blined randomized controlled trial

Department of Oral and Maxillofacial Surgery, Faculty of Dentistry , Chiangmai university0 个研究点目标入组 20 人开始时间: 2022年7月15日最近更新:
适应症

试验速览

阶段
4 期
发起方
入组人数
20

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
10 Years 至 60 Years(—)
性别
All

入选标准

  • 1. Participants who have been diagnosed with premolar teeth extraction in the upper jaw on both sides
  • 2. No gender and age limit
  • 3. Be in good health or AHA Classifications I and II
  • 4. Not during the first or third trimester of pregnancy or breast-feeding.
  • 5. Able to receive treatment and follow up at specified intervals

排除标准

  • 1. Participants who have any hypersensitivity to amide local anesthetics or components of anesthetics.
  • 2. the premolar teeth have pathological signs and pain or there are periapical lesions.
  • 3. Participants have any soft tissue infection.
  • 4. Participants who received NSAIDs and acetaminophen 24 hours before the study.

研究者

发起方
Department of Oral and Maxillofacial Surgery, Faculty of Dentistry , Chiangmai university

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