Analysis of the Association of Products for the Treatment of Cervical Dentin Hypersensitivity
Overview
- Phase
- N/A
- Intervention
- Resin modified glass ionomer
- Conditions
- Hypersensitivity Dentin
- Sponsor
- Federal University of Uberlandia
- Enrollment
- 140
- Locations
- 1
- Primary Endpoint
- Level of cervical dentin hypersensitivity, measured by visual analog scale
- Status
- Completed
- Last Updated
- 9 years ago
Overview
Brief 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.
Detailed Description
Cervical dentin hypersensitivity is a painful condition and is a clinical challenge due to different treatment strategies available. 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. A hundred forty teeth of healthy patients of both sexes were selected. Visual Analog Scale was used pain (VAS) to measure the intensity of the patient's pain. The teeth will be randomly divided into 7 different groups according to the desensitization treatment under study: 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.
Investigators
PAULO VINICIUS SOARES
Professor
Federal University of Uberlandia
Eligibility 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.
Arms & Interventions
RMGI and KF
Resin modified glass ionomer and potassium nitrate and sodium fluoride 2%; an application of the two associated products, every 48 hours; 4 sessions.
Intervention: Resin modified glass ionomer
Resin modified glass ionomer (RMGI)
Resin modified glass ionomer; an application every 48 hours; 4 sessions.
Intervention: Resin modified glass ionomer
Potassium Nitrate 2% (KF)
Potassium Nitrate and Sodium fluoride 2%; an application every 48 hours; 4 sessions.
Intervention: Potassium Nitrate 2%
Low level laser therapy - GaAlAs (LLLT)
Low level laser therapy - GaAlAs; an application every 48 hours; 4 sessions.
Intervention: Low level laser therapy
RMGI and KF
Resin modified glass ionomer and potassium nitrate and sodium fluoride 2%; an application of the two associated products, every 48 hours; 4 sessions.
Intervention: Potassium Nitrate 2%
RMGI and LLLT
Resin modified glass ionomer and Low level laser therapy - GaAlAs; an application of the two associated products, every 48 hours; 4 sessions.
Intervention: Resin modified glass ionomer
RMGI and LLLT
Resin modified glass ionomer and Low level laser therapy - GaAlAs; an application of the two associated products, every 48 hours; 4 sessions.
Intervention: Low level laser therapy
KF and LLLT
Potassium Nitrate and Sodium fluoride 2% and Low level laser therapy - GaAlAs; an application of the two associated products, every 48 hours; 4 sessions.
Intervention: Potassium Nitrate 2%
KF and LLLT
Potassium Nitrate and Sodium fluoride 2% and Low level laser therapy - GaAlAs; an application of the two associated products, every 48 hours; 4 sessions.
Intervention: Low level laser therapy
RMGI, KF, LLLT
Resin modified glass ionomer, potassium nitrate and sodium fluoride 2% and Low level laser therapy - GaAlAs ; an application of the three associated products, every 48 hours; 4 sessions.
Intervention: Resin modified glass ionomer
RMGI, KF, LLLT
Resin modified glass ionomer, potassium nitrate and sodium fluoride 2% and Low level laser therapy - GaAlAs ; an application of the three associated products, every 48 hours; 4 sessions.
Intervention: Potassium Nitrate 2%
RMGI, KF, LLLT
Resin modified glass ionomer, potassium nitrate and sodium fluoride 2% and Low level laser therapy - GaAlAs ; an application of the three associated products, every 48 hours; 4 sessions.
Intervention: Low level laser therapy
Outcomes
Primary Outcomes
Level of cervical dentin hypersensitivity, measured by visual analog scale
Time Frame: 24 weeks
Evaluate the reduction in Cervical Dentin Hypersensitivity with a 24 weeks follow up.