Analysis of the Association of Products for the Treatment of Cervical Dentin Hypersensitivity
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 140
- 试验地点
- 1
- 主要终点
- Level of cervical dentin hypersensitivity, measured by visual analog scale
研究概览
简要总结
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.
详细描述
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.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Participant, Outcomes Assessor)
入排标准
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •presence of dentin exposure lesions with clinical diagnosis of moderate or severe tooth sensitivity
- •good oral hygiene.
排除标准
- •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.
研究组 & 干预措施
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.
干预措施: Resin modified glass ionomer (Drug)
Resin modified glass ionomer (RMGI)
Resin modified glass ionomer; an application every 48 hours; 4 sessions.
干预措施: Resin modified glass ionomer (Drug)
Potassium Nitrate 2% (KF)
Potassium Nitrate and Sodium fluoride 2%; an application every 48 hours; 4 sessions.
干预措施: Potassium Nitrate 2% (Drug)
Low level laser therapy - GaAlAs (LLLT)
Low level laser therapy - GaAlAs; an application every 48 hours; 4 sessions.
干预措施: Low level laser therapy (Procedure)
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.
干预措施: Potassium Nitrate 2% (Drug)
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.
干预措施: Resin modified glass ionomer (Drug)
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.
干预措施: Low level laser therapy (Procedure)
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.
干预措施: Potassium Nitrate 2% (Drug)
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.
干预措施: Low level laser therapy (Procedure)
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.
干预措施: Resin modified glass ionomer (Drug)
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.
干预措施: Potassium Nitrate 2% (Drug)
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.
干预措施: Low level laser therapy (Procedure)
结局指标
主要结局
Level of cervical dentin hypersensitivity, measured by visual analog scale
时间窗: 24 weeks
Evaluate the reduction in Cervical Dentin Hypersensitivity with a 24 weeks follow up.
次要结局
未报告次要终点
研究者
PAULO VINICIUS SOARES
Professor
Federal University of Uberlandia