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临床试验/IRCT201203124224N19
IRCT201203124224N19已完成2 期

Assessing and comparing of Midazolam/Propofol and Ketamin/Propofol intravenouses sedation in anxiety children for dental treatment

Vice chancellor for Research of Isfahan university of medical sciences0 个研究点目标入组 32 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
32

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
6 years 至 8 years(—)
性别
All

入选标准

  • Inclusion Criteria: Children ages 6-8? Uncooperative 1negetive in Frankel grading? No specific disease? ASA I? No need to extraction? Treatment needs only on left side of upper jaw? No contraindication of sedation.
  • Exclusion criteria: Emergency event during study? Dental treatment more than 45 minutes.

排除标准

  • 未提供

研究者

发起方
Vice chancellor for Research of Isfahan university of medical sciences

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