Single Application of Desensitizing Pastes as Dentin Sensitivity Treatment

NCT ID: NCT02018783

Last Updated: 2013-12-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

138 participants

Study Classification

INTERVENTIONAL

Study Start Date

2013-04-30

Study Completion Date

2013-08-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The aim of this study was to evaluate the efficacy of three desensitizing toothpastes for immediate and intermediate-term relief of CDH, when compared with a control toothpaste. One hundred and thirty-eight hypersensitive teeth were diagnosed and randomized into four groups according to the therapeutic agent of each desensitizing cream tested: 1) strontium acetate and calcium carbonate, 2) calcium carbonate and arginine 8%, 3) calcium phosphate nanoparticles and 4) a control toothpaste. The desensitizing creams were applied according to the manufacturer's instructions. Cervical dentin hypersensitivity was assessed at baseline, immediately, 24 hours and 30 days after the treatment. Cold and evaporative tests were used to assess the sensitivity level.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Dentine Hypersensitivity

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Caregivers Investigators

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Sensodyne

Digital application for 60 seconds.

Group Type EXPERIMENTAL

Sensodyne

Intervention Type PROCEDURE

Digital application for 60 seconds.

Colgate

Slow-speed handpiece with a Robson brush for 3 seconds by repeating the procedure

Group Type EXPERIMENTAL

Colgate

Intervention Type PROCEDURE

Slow-speed handpiece with a Robson brush for 3 seconds by repeating the procedure

Nano P

Slow-speed handpiece with a Robson brush for 10 seconds

Group Type EXPERIMENTAL

Nano P

Intervention Type PROCEDURE

Slow-speed handpiece with a Robson brush for 10 seconds

Cocorico

Digital application for 60 seconds

Group Type PLACEBO_COMPARATOR

Cocorico

Intervention Type PROCEDURE

Digital application for 60 seconds

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Colgate

Slow-speed handpiece with a Robson brush for 3 seconds by repeating the procedure

Intervention Type PROCEDURE

Sensodyne

Digital application for 60 seconds.

Intervention Type PROCEDURE

Nano P

Slow-speed handpiece with a Robson brush for 10 seconds

Intervention Type PROCEDURE

Cocorico

Digital application for 60 seconds

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* subjects 18 years or older
* in good general and oral health; have complaint of CDH in teeth distributed in all 4 quadrants
* not making use of desensitizing agents
* not having undergone periodontal treatment over the past 3 months
* respond to evaporative stimulus with a score ≥ 1.5 cm on VAS

Exclusion Criteria

* patients who presented restorations and caries near the exposed dentin of the hypersensitive teeth
* who made frequent use of painkillers, anti-inflammatory and antidepressants drugs
Minimum Eligible Age

22 Years

Maximum Eligible Age

48 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Federal University of São Paulo

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Olga Flecha

PhD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Olga D Flecha, PhD

Role: PRINCIPAL_INVESTIGATOR

Federal University of São Paulo

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Periodontics Clinic, Department of Dentistry

Diamantina, Minas Gerais, Brazil

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Brazil

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

dessensibilizantes

Identifier Type: -

Identifier Source: org_study_id