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临床试验/NCT06855940
NCT06855940进行中(未招募)不适用

Evaluation of the Tooth Sensitivity and Whitening Effects of Calcium, Hydroxyapatite and Fluoride Containing Tooth Whitening Agents

Betül Tokat1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年2月2日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
60
试验地点
1
主要终点
Change in tooth color within 1 year after whitening

研究概览

简要总结

The goal of this clinical study is to evaluate the success of different whitening agents in whitening teeth in healthy volunteers aged 18-50. Also, patients' tooth sensitivity will be assessed after application. The main questions it aims to answer are:

Is the teeth whitening success of different whitening agents similar? Did participants develop tooth sensitivity to whitening agents? The researchers will compare the whitening success of 3 different whitening agents and changes in tooth sensitivity within 1 year after application.

Participants:

Whitening agent will be applied in the clinic Visit our clinic for checkups and records after 1 week, 2 weeks, 1 month, 2 months, 4 months , 6 months and 1 year after application

详细描述

The participants in the study were healthy volunteers between the ages of 18-50. The number of volunteers was determined by using other studies similar to this study. There are 60 volunteers in three groups, 20 volunteers in each group. A different whitening agent is applied to each group by the researcher.

The researcher did not include volunteers with poor oral hygiene, smoking, tooth sensitivity, caries, or medication use in the study.

The researcher began the study by performing color measurement and sensitivity assessment before the procedure. Then he applied the whitening agent. The volunteers who underwent the whitening procedure will be evaluated in terms of both color measurements and sensitivity changes at the end of the treatment, 1st week, 2nd week, 1st month, 2nd month, 4th month, 6th month, and 1st year control sessions.

Each patient has their own evaluation form. There are different fields for both color and sensitivity in the form according to the control dates. All numerical data are recorded in their own fields.

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
Single (Participant)

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Vital teeth
  • •Healthy gums
  • •No tooth sensitivity
  • •External discoloration ( tea,coffee..)
  • •Good oral hygiene
  • •No allergy to the material to be used

排除标准

  • •Decayed and devital teeth
  • •Presence of gingival bleeding
  • •History of trauma
  • •Presence of fractures, cracks and aesthetic restoration

研究组 & 干预措施

Group A

Active Comparator

20 random patients( Whitening agent containing fluoride and 40% active ingredients)

干预措施: Bleaching Agents (Other)

Group B

Active Comparator

20 random patients(Whitening agent containing calcium and 35% active ingredients)

干预措施: Bleaching Agents (Other)

Group C

Active Comparator

20 random patients(Whitening agent containing hydroxyapatite and 18% active ingredients)

干预措施: Bleaching Agents (Other)

结局指标

主要结局

Change in tooth color within 1 year after whitening

时间窗: through study completion, an average of 1 year

Measurement and recording of numerical values of tooth color with vita easyshade device

Change in tooth sensitivity after whitening within 1 year

时间窗: through study completion, an average of 1 year

Numerical measurement of sensitivity after bleaching with VAS (visual analog scale)

次要结局

未报告次要终点

研究者

发起方
Betül Tokat
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Betül Tokat

research assistant

TC Erciyes University

研究点 (1)

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