Dentin Sensitivity

4

Review clinical trials related to Dentin Sensitivity. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Real-World Study of a Calcium Sodium Phosphosilicate Anti-Sensitivity Toothpaste for Dentin Hypersensitivity Relief

The aim of this study is to evaluate the impact of a commercially available desensitizing dentifrice containing 5 percent (%) Calcium sodium phosphosilicate (CSPS) on oral health related quality of life (OHrQoL) in a DH (Dentin Hypersensitivity) population in a real-world setting.

Participants needed: 500
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: HALEONUpdated: Mar 11, 2026Locations: 1
Eligibility criteria

Participant who has provided consent indicating they have been informed of all p... [+3]

Participant who has been/is on multiple prescription medications to treat severe... [+6]

Status: Not yet recruiting

Effect of an Experimental Cannabidiol Gel on Tooth Sensitivity

The goal of this clinical trial will be to evaluate the effect applying an experimental gel based on cannabidiol oil (CBD) on tooth sensitivity induced by tooth bleaching with 35% hydrogen peroxide (HP). Volunteers will be selected and allocated to the following groups: GP - placebo gel, GCBD - experimental cannabidiol gel and GKF - Potassium Nitrate and Sodium Fluoride Gel. In each group, the corresponding desensitizing gel will be applied to on the teeth for 10 minutes. All groups will then undergo in-office whitening treatment with 35% hydrogen peroxide. Patients will be instructed to record tooth sensitivity on a daily basis during the 21 days of follow-up. Pain intensity will be measured using a visual analog scale (VAS), while the risk of developing sensitivity will be recorded after each session of the whitening procedure, with two response option.

Participants needed: 75
Trial details
Phase: Phase 1Age: 18-40Biological sex: AllType: InterventionalSponsor: Universidade Federal do ParaUpdated: Jun 18, 2025Locations: 1
Eligibility criteria

Participants must have at least 28 teeth in the cavity [+1]

active caries or periodontal disease [+10]

Status: Not yet recruiting

Efficacy and Safety Assessment of Experimental Bleaching Agents

Tooth bleaching is widely used to treat the colors of teeth. This study compares the efficiency of two experimental bleaching gels, with and without nanoparticles, and with and without light activation versus two commercial bleaching products of low and high concentrations. The objective is to evaluate tooth color change, sensitivity, and patient satisfaction in patients with moderate yellowing of their teeth. Methods: This is a randomized controlled trial that will include 120 participants aged 18-65 years. Participants will be randomly assigned to one of 12 treatment groups: Gel A (with or without nanoparticles, with or without light), Gel B (with or without nanoparticles, with or without light), Whiteness HP 35% (with or without light) and Whiteness Automixx 6% (with or without light). The primary outcome is tooth color change, measured using a commercially-available equipment. Secondary outcomes will include tooth sensitivity and patient satisfaction. Randomization will be computer-generated. Results: The study is expected to show differences in color change between the experimental and commercial gels. Tooth sensitivity and patient satisfaction will be evaluated to determine the overall effectiveness and safety of the treatments. Conclusions: This trial will provide information into the whitening efficacy of two experimental gels compared to two widely used commercial products.

Participants needed: 240
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: University of OklahomaUpdated: Jan 31, 2025Locations: 1
Eligibility criteria

Age: 18-65 years old. [+4]

Pregnant or breastfeeding women. [+4]

Status: Recruiting

A Clinical Trial to Compare Lasotronix Alone or in Combination With CPP-ACP to Treat DH

Dentin hypersensitivity (DH) is defined as sharp pain of a shorter duration arise from exposed dentin in response to several chemicals and thermal or tactile stimuli that cannot be ascribed to other dental defects". DH has a prevalence rate ranging from 1.3% to 92.1%, commonly affecting old ages. The use of laser has opened new dimensions in the treatment of DH. To the author's knowledge, not much research work has been conducted using LASOTRONIX as a treatment modality with CPP-ACP. Therefore, this research aims to determine the effectiveness of Casein phospho peptide paste (CPP-ACP) used alone or combined with a diode laser (LASOTRONIX).

Participants needed: 120
Trial details
Age: 25-65Biological sex: AllType: InterventionalSponsor: Dow University of Health SciencesUpdated: Jul 26, 2024Locations: 1
Eligibility criteria

Patients of either gender, with ages between 25-65 years [+1]

History of desensitizing therapy on the affected tooth/teeth in last six months... [+4]