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临床试验/CTRI/2022/03/041381
CTRI/2022/03/041381已完成3 期

Comparative Evaluation of diode laser with and without a desensitizing agent in the treatment of dentinal hypersensitivity : A randomized controlled clinical trial

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试验速览

阶段
3 期
状态
已完成
发起方
A

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

  • 1. Patients who are cooperative, motivated and willing to participate in the study will be included.
  • 2. Patients who will be having sensitive teeth that show abrasion, erosion or gingival recession with exposure of cervical dentin.
  • 3. Patients having good systemic health with clinically elicitable dentinal hypersensitivity who will be reliable in their response to test measurements.
  • 4. Patients who will be willing and available for recall follow ups.
  • 5. Patients with no known allergies to commercial dental products.
  • 6. History of no use of desensitizing toothpaste or mouthwash past 3 months.
  • 7. Patients who have not received any professional desensitizing therapy for dentinal
  • hypersensitivity in the past 3 months.
  • 8. Patients who will be having minimum 1 and maximum 32 hypersensitive teeth will be included in the study.

排除标准

  • 1.Patients having deep dental caries or large restorations on the selected hypersensitive teeth.
  • 2. Patients who will be having cracked or chipped teeth with hypersensitivity.
  • 3. Patients with cervical restorations or premature contacts on the hypersensitive teeth.
  • 4. Patients who will be having chronic disease with daily pain episodes, and on any analgesics / antiâ??inflammatory, anticonvulsive, anti-histaminic, tranquilizing or sedative medication drugs in the last 72 hours.
  • 5.Patients who are lactating or are pregnant women .
  • 6. Patients with any cardio-circulatory disease or having cardio pacemaker.
  • 7. Patients with the habit of smoking or alcohol intake.
  • 8.Patients who will not consent to participate or to attend the follow up recall appointments.
  • 9.Excessive dietary or environmental exposure to acids.

研究者

发起方
A

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