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
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.
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