Treatment of Tooth Sensitivity With the Use of Biorepair Toothpaste

Qassim University72 enrolled

Overview

The purpose of this clinical study is to evaluate the effect of desensitizing toothpaste containing zinc-carbonate hydroxyapatite nanocrystals in reducing or controlling DH after 8 weeks of treatment

This clinical study design is an 8-week single center, before and after use of desensitize dentifrice. This study will conducted in the College of Dentistry Qassim University. 72 patients surfing from DH, include in the study fulfill the inclusion criteria. All subjects 20 to 70 years of age in good health, and must have 2 teeth with DH, will be included in this study. Screening will be performed for the selection of patients, which fulfill the inclusion criteria. Baseline data will be recorded and Sensitivity was assessed by air-blast sensitivity, using Schiff Sensitivity Scale (SSS). Sensitivity was assessed by air-blast sensitivity, using Schiff Sensitivity Scale (SSS) described as follows. 0 = Subject does not respond to air stimulus 1. = Subject responds to air stimulus but does not request discontinuation of stimulus 2. = Subject responds to air stimulus and requests discontinuation or moves from stimulus 3. = Subject responds to air stimulus, considers stimulus to be painful, and requests discontinuation of the stimulus

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Dentinal Hypersensitivity

Interventions

Single arm clinical studyOTHER

Participants will be treated with desensitizing toothpaste containing zinc-carbonate hydroxyapatite nanocrystals (Zn-CHA) for 8 weeks.

Eligibility

Sex: ALLMin age: 20 YearsMax age: 70 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * All male and female subjects 20 to 70 years of age * All subjects in good health * All subjects must have 2 teeth with DH, only incisors, canine and premolars were included with the exposed cervical dentin (facial surfaces). All participants of the study having Schiff Sensitivity Scale score of 2 \& 3 Exclusion Criteria: * Subjects with deep carious teeth, defective restorations * Any pathological lesion * Periodontal disease, mobile teeth, cracked enamel, orthodontic appliances, * Periodontal pockets \>4mm * Subjects using pain control medicines, sensitive toothpaste * Pregnant or lactating women

Locations (1)

College of Dentistry Qassim University

Buraidah, Al Qassim, Saudi Arabia

Outcomes

Primary Outcomes

Dentine hypersensitivity (DH) evaluation by means of air-blast sensitivity test, using Schiff Sensitivity Scale (SSS) after 4 weeks.

This will be assessed using Schiff Sensitivity Scale (SSS) score difference from the baseline, that will be determined immediately before product use and then after 4 weeks of daily brushing with the test sensitive toothpaste. Tooth sensitivity score was assessed by air-blast sensitivity, using Schiff Sensitivity Scale (SSS) as follows: 0 = Subject does not respond to air stimulus, 1 = Subject responds to air stimulus but does not request discontinuation of stimulus, 2 = Subject responds to air stimulus and requests discontinuation or moves from stimulus, 3 = Subject responds to air stimulus, considers stimulus to be painful, and requests.

Time frame: 4 Weeks

Secondary Outcomes

Dentine hypersensitivity (DH) evaluation by means of air-blast sensitivity test, using Schiff Sensitivity Scale (SSS) after 8 weeks

This will be assessed using Schiff Sensitivity Scale (SSS) score difference from the baseline, that will be determined immediately before product use and then after 8 weeks of daily brushing with the test sensitive toothpaste. Tooth sensitivity score was assessed by air-blast sensitivity, using Schiff Sensitivity Scale (SSS) as follows: 0 = Subject does not respond to air stimulus, 1 = Subject responds to air stimulus but does not request discontinuation of stimulus, 2 = Subject responds to air stimulus and requests discontinuation or moves from stimulus, 3 = Subject responds to air stimulus, considers stimulus to be painful, and requests.

Time frame: 8 Weeks

Data from ClinicalTrials.gov

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