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临床试验/CTRI/2025/07/090839
CTRI/2025/07/090839
尚未招募
不适用

COMPARATIVE EVALUATION OF DIFFERENT METHODS FOR THE TREATMENT OF DENTIN HYPERSENSITIVITY: A RANDOMIZED CLINICAL TRIAL

Dr Bhavana Shikari1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2025年7月30日最近更新:

概览

阶段
不适用
状态
尚未招募
发起方
Dr Bhavana Shikari
入组人数
90
试验地点
1
主要终点
Reduction in Dentin Hypersensitivity

概览

简要总结

This study will be a randomized, split-mouth, controlled clinical trial designed to evaluate the efficacy of three different agents in the treatment of dentin hypersensitivity. A total of 90 teeth with dentin hypersensitivity will be included. Each patient’s mouth will be divided into three quadrants, with each receiving one of the two test agents (HIGH-POWER DIODE LASER , RESIN BASED LIGHT CURE DESENSITIZING AGENT). The third quadrant may serve as a positive control with MI VARNISH. Sensitivity levels will be assessed at baseline (T0) using standardized methods such as the Visual Analog Scale (VAS), air-blast test, or tactile test. Follow-up evaluations will be conducted at Immediately (T1),1 week post-treatment(T2) , 3 months post-treatment (T3), and after 6 months(T4) to monitor changes in sensitivity levels and compare the effectiveness of the three agents. This split-mouth design will minimize individual variability and allow for direct intra-patient comparisons of the treatments

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant Blinded

入排标准

年龄范围
18.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • Patients who are 18 to 70 years old with complaints of DHS for more than 1 year Stimulated DHS more than 6 on the visual analogue scale DHS that affected 3 nonadjacent teeth of different mouth semiarches Patients with NCCL or Gingival recession (Miller Class I and II gingival recession).

排除标准

  • Patients who have undergone Periodontal surgery in the last 3 months Use of desensitizing paste or any desensitizing treatment in the last 3 months Patients undergoing orthodontic treatment Pregnant or breastfeeding women Teeth with caries pulpitis congenital anomalies fracture or occlusal interferences.

结局指标

主要结局

Reduction in Dentin Hypersensitivity

时间窗: 18 months

次要结局

  • Long term clinical efficacy of desentizing methods(18 months)

研究者

发起方
Dr Bhavana Shikari
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Bhavana Shikari

Government Dental College and Hospital Jamnagar

研究点 (1)

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