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临床试验/CTRI/2018/04/013038
CTRI/2018/04/013038已完成2 期

A Clinical trial to evaluate the efficacy and comparison of a dentifrice containing Sodium Fluoride; 8% Strontium Acetate, Strontium Acetate (in Herbal Base) and two different Herbal dentifrices in reducing Dentinal Hypersensitivity

Dabur India Limited0 个研究点目标入组 139 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
已完成
入组人数
139

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

入选标准

  • Subjects with dental hypersensitivity complaints

排除标准

  • 1. Subjects who had dental pathology causing pain similar to cervical dentinal hypersensitivity (such as teeth with caries, the presence of orthodontic appliances and restorations and/or the presence of a history of periodontal surgery in the area of the tooth during the previous three months)
  • 2. Subjects who had taken any medication
  • 3. Subjects who received professional treatment with desensitizing agents in the previous six months
  • 4. Subjects who received any treatment in the past 3 months
  • 5. Subjects who were pregnant or lactating
  • 6. Subjects who had any systemic diseases and/or the presence of a vital bleaching history

研究者

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