Completed

Phase Not Applicable
All Genders
ID02931734

Analysis of the Association of Products for the Treatment of Cervical Dentin Hypersensitivity

Led by Federal University of Uberlandia · Updated on 2016-10-14

140

Participants Needed

1

Research Sites

25 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of this study is through a randomized clinical trial, double blind, splith-mouth, evaluate the various types of protocols and clinical efficacy in the reduction or even elimination of dentinal hypersensitivity by the agents Desensibilize KF - FGM Dental Products, Clinpro - 3M Company, Minnesota - USA, Photon Laser III - DMC, Brazil, Desensibilize KF and laser, Desensibilize KF and Clinpro, laser and Clinpro and the association of all products. Data will be collected, tabulated and submitted to statistical analysis.

CONDITIONS

Brief Title

Assessment of Different Protocols for Cervical Dentin Hypersensitivity Treatment

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • presence of dentin exposure lesions with clinical diagnosis of moderate or severe tooth sensitivity
  • good oral hygiene.
Not Eligible

You will not qualify if you...

  • cavities,
  • presence of periodontal disease and or parafunctional habits,
  • cracks or enamel fractures,
  • extensive or unsatisfactory restorations,
  • recent restorations involving the labial surface,
  • dentures,
  • orthodontics.

Trial Site Locations

Total: 1 location

1

Federal University of Uberlandia

Uberlândia, Minas Gerais, Brazil, 38400-000

Status Unknown

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

7

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Published Research Related To This Trial