跳至主要内容
临床试验/PACTR202309545839091
PACTR202309545839091招募中Unknown

A Comparative evaluation of the efficiency of visual tactile method, caries detector dye and fluorescence device in diagnosing residual caries after cavity preparation”.

SELF0 个研究点目标入组 90 人开始时间: 2023年8月30日最近更新:

试验速览

阶段
Unknown
状态
招募中
发起方
SELF
入组人数
90

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
19 Year(s) 至 44 Year(s)(—)
性别
All

入选标准

  • 1.All consecutive adult subjects above the age of 18, in good general health, presenting at the oral diagnosis clinic.
  • 2.Adults with at least one permanent molar/ premolar diagnosed to have DC
  • 3.Adults with at least one permanent molar/ premolar diagnosed to have DC, in dentine, without irreversible pulpal damage or periapical involvement and with sufficient extension to allow DIAGNOdent placement within the excavation

排除标准

  • 1.Carious lesions associated with signs and symptoms of irreversible pulp inflammation and or periapical inflammation. These will also include tooth/teeth with:
  • a.History of spontaneous pain
  • b.History of swelling
  • c.Presence and/or preceding history of discharging sinus
  • d.Tenderness on palpation and/or percussion
  • e.Grossly broken down tooth
  • f.Periradicular or periapical radiolucency.
  • h.Advanced periodontal diseases: grade III mobility
  • i.True negative response to pulp sensibility test
  • j.Coronal radiolucency due to caries that appears to communicate with pulp, with or without symptoms
  • k.Pulpal bleeding (exposure) during caries excavation
  • l.Traumatized teeth
  • m.Third molars
  • 2.Subjects that have been on antibiotics or steroids within a period of three months prior to the study period.
  • 3.Pregnant women.
  • 4.Subjects that decline to consent to the treatment procedure, despite elaborate explanations of the treatment protocols.

研究者

发起方
SELF

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