跳至主要内容
临床试验/CTRI/2026/03/107015
CTRI/2026/03/107015尚未招募2 期

To evaluate the clinical effectiveness of DR 32 herbal tooth paste in reducing dentinal hypersensitivity A Randomized Controlled Trial

Dr Shruthi MS2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2026年4月10日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
40
试验地点
2

研究概览

简要总结

This study is a randomized, parallel-group controlled trial conducted at the Department of Periodontology, Subbaiah Institute of Dental Sciences, Shivamogga. The primary purpose of the study is to evaluate the clinical effectiveness and safety of 0.5% DR-32 herbal toothpaste in reducing dentin hypersensitivity.

A total of 40 systemically healthy participants with dentin hypersensitivity will be recruited and randomly allocated into two groups (20 per group). All participants will undergo scaling and root planing, followed by assignment to either DR-32 herbal toothpaste or calcium sodium phosphosilicate–based toothpaste for a period of two weeks. Dentin hypersensitivity will be assessed at baseline, 15 days, and 30 days using tactile, air blast, and cold-water tests. Objective assessment will be performed using the Schiff sensitivity scale, and subjective assessment will be recorded using the Visual Analog Scale (VAS).

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Systemically healthy Minimum of 2 adjacent sensitive teeth Minimum of 20 residual teeth Patient with good Oral Hygiene.

排除标准

  • Smokers and Tobacco chewers Patients with allergy due to materials used in study Participants who develop any signs of irritation or allergic reaction to the study materials during the study period will be withdrawn and provided appropriate care Patients who have used Analgesic for any systemic illness within 72 hours prior to baseline examination will be excluded Patients with several dental caries defective restorations Patients with existing use of toothpaste for sensitive teeth Patient who went procedures periodontal surgery for root coverage class V resin filling and desensitizing agent application in past 1 month DH caused by whitening treatment or use of whitening toothpastes.

研究者

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

DR Shruthi MS

Subbaiah Institiute of Dental Sciences

研究点 (2)

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