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临床试验/IRCT20230210057378N1
IRCT20230210057378N1招募中3 期

Comparing anesthetic efficacy of 4% Articaine and 2% Lidocaine as buccal infiltration in mandibular ramus block harvesting for bone augmentation in implant patients requirin bone augmentation

Qazvin University of Medical Sciences0 个研究点目标入组 20 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
招募中
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
18 years 至 65 years(—)
性别
All

入选标准

  • People between 18 and 65 years old
  • Systemically healthy people
  • Having the ability to fill out questionnaires
  • People with bone defects in the edentulous area and candidate for bone graft
  • People who need implants in the upper jaw or the opposite side of the bone removal area in the lower jaw (contralateral)

排除标准

  • Presence of an abscess or any pathological lesion at the injection site
  • History of diabetes, cardiovascular diseases, hypertension and kidney diseases
  • History of allergy to Lidocaine or Articaine local anesthetics
  • Consumption of alcohol or any pain reliever
  • Mentally unable to give informed consent
  • pregnancy and breastfeeding

研究者

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