Assessment of Different Protocols for Cervical Dentin Hypersensitivity Treatment

• Status: Completed
• Trial end date: 2015-07-01
• Target enrollment: 0
• Participant gender: All

Summary

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.

• Phase: N/A
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Federal University of Uberlandia

Criteria

Inclusion Criteria:

• presence of dentin exposure lesions with clinical diagnosis of moderate or severe tooth sensitivity

• good oral hygiene.

Exclusion Criteria:

• 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.