Erciyes University
Kayseri, Melikgazi, 38000, Turkey (Türkiye)
NCT Number: NCT06855940
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
This study is active but is not currently recruiting participants.
18 year–50 year
All sexes
Interventional
Not applicable
Kayseri, Melikgazi, 38000, Turkey (Türkiye)
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.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
whitening agent containing fluoride and 40% hydrogen peroxide
Time frame: through study completion, an average of 1 year
Measurement and recording of numerical values of tooth color with vita easyshade device
Time frame: through study completion, an average of 1 year
Numerical measurement of sensitivity after bleaching with VAS (visual analog scale)
Betül Tokat
Other
Evaluation of the Tooth Sensitivity and Whitening Effects of Calcium, Hydroxyapatite and Fluoride Containing Tooth Whitening Agents
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07736599
Behavior, Behavioral Symptoms
Amasya, Turkey (Türkiye)
View Trial DetailsNCT00410241
Arterial Occlusive Diseases, Arteriosclerosis
Bethesda, Maryland, United States
View Trial DetailsNCT07646548
Healthy Volunteers
Hialeah, Florida, United States
View Trial DetailsNCT07567781
Healthy Volunteers
Grayslake, Illinois, United States
View Trial Details