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临床试验/NCT04548674
NCT04548674已完成不适用

Effect of Different Desensitizing Protocols on the Pulp Inflammatory Response in Bleached Teeth: A Randomized Clinical Trial.

Universidade Federal do Para1 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2018年8月20日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
18
试验地点
1
主要终点
Pulp inflammation

研究概览

简要总结

This randomized, controlled, blinded clinical trial evaluated the effectiveness of different desensitizing protocols in preventing pulp inflammation after bleaching treatment with 35% hydrogen peroxide (PH) (Whiteness PH 35%).

详细描述

Thirty healthy third human molars extracted by orthodontic indication were randomized and allocated into five groups (n = 6): CN (negative control): without intervention; CP (Positive control): PH; PMB: PH + photobiomodulation with low power laser; CPP: PH + casein phosphopeptide phosphopeptide amorphous calcium phosphate (CPP-ACPF); NANO: PH + nanohydroxyapatite. The office whitening was performed in two sessions with a single application of 45 min and an interval of 48 hours between them. Pulp tissues were removed for immunohistochemical analysis. Immunostaining was performed for Caspase 3 using an Axio Scope.A1 microscope.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Sequential
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
20 Years 至 26 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Lower third molars class I position A
  • •Maxillary third molars horizontal position A
  • •Absence of caries and enamel fracture
  • •Absence of periodontal disease
  • •Extraction of third molars for orthodontic reasons
  • •No allergy to the anesthetic and positive pulp sensitivity test

排除标准

  • •Calcification in the middle third of the root
  • •Drug users or smokers
  • •Patients who have already done whitening
  • •Root apex with incomplete formation and patients with systemic problems that would make surgery impossible

研究组 & 干预措施

CPP Group

Experimental

Whiteness HP 35% + CPP

干预措施: Whiteness HP 35% (Other)

CPP Group

Experimental

Whiteness HP 35% + CPP

干预措施: Whiteness HP 35% + CPP (Other)

Positive Control Group

Placebo Comparator

Whiteness HP 35%

干预措施: Whiteness HP 35% (Other)

Laser Group

Experimental

Whiteness HP 35% + Laser

干预措施: Whiteness HP 35% (Other)

Laser Group

Experimental

Whiteness HP 35% + Laser

干预措施: Whiteness HP 35% + LASER (Device)

Nano Group

Experimental

Whiteness HP 35% + NANO

干预措施: Whiteness HP 35% (Other)

Nano Group

Experimental

Whiteness HP 35% + NANO

干预措施: Whiteness HP 35% + NANO (Other)

Negative Control

No Intervention

Without intervention

结局指标

主要结局

Pulp inflammation

时间窗: 3 days After extraction of third molars

Evaluation of pulp inflammation through immunohistochemistry of the third molar whitening or not

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Cecy Martins Silva

Professor Clínico

Universidade Federal do Para

研究点 (1)

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