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临床试验/IRCT2016122231473N1
IRCT2016122231473N1已完成未知

Comparison of post-operative pain following pulpectomy of vital deciduous teeth in one or two sessions: a randomized clinical trial

Research and Technology Vice Chancellry, Kerman University of Medical Sciences0 个研究点目标入组 100 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
100

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 12 years(—)
性别
All

入选标准

  • vital decidious teeth with active bleeding during access cavity preparation,  lack of clinical and radiographic evidence of pulpal necrosis,  resorption of less than two third of the root length, restoration possible, cooperative child, at least one molar with evidence of irreversible pulpitis , e.g. sensitivity to cold or hot stimulus.
  • Exclusion criteria: child with systemic diseases, follicular or dentigerous cyst below decidous tooth, pathologic resorption of at least one third of root length with fistulous sinus tract, resorption of more than two third of root length, isolation of tooth not possible, advanced internal resorption, periradicular lucency involving permanent tooth bud.

排除标准

  • 未提供

研究者

发起方
Research and Technology Vice Chancellry, Kerman University of Medical Sciences

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