Bleaching Sensitivity, Discoloration of Teeth, Healthy Volunteers
Conditions
Keywords
Bleaching Agents, Bleaching agent \( BOOST 40%\), Bleaching teeth, Discoloration of Teeth, Sensitivity, Tooth
Brief summary
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
Detailed description
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.
Interventions
OTHERBleaching Agents
whitening agent containing fluoride and 40% hydrogen peroxide
Sponsors
TC Erciyes University
Scientific Research Projects
Betül Tokat
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Intervention model description
Group A: X bleaching agents Group B: Y bleaching agents Group C: Z bleaching agents
Eligibility
Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes
Inclusion criteria
* Vital teeth * Healthy gums * No tooth sensitivity * External discoloration ( tea,coffee..) * Good oral hygiene * No allergy to the material to be used
Exclusion criteria
* Decayed and devital teeth * Presence of gingival bleeding * History of trauma * Presence of fractures, cracks and aesthetic restoration * Smoking
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in tooth color within 1 year after whitening | 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 | through study completion, an average of 1 year | Numerical measurement of sensitivity after bleaching with VAS (visual analog scale) |
Countries
Turkey (Türkiye)
Outcome results
None listed