The primary objective of this 12-week study is to test BlueCheck's ability to identify enamel lesions consistently, and its ability to track changes in these lesions over time.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
5
BlueCheck, a carious lesion detection formulated device, will be used to track enamel lesions for patients who are newly receiving a high fluoride toothpaste.
This clinical study is testing the ability of BlueCheck to detect enamel lesions over time. In order to show changes in lesions, subjects will be prescribed Prevident 5000ppm Booster Plus Toothpaste
Dental Dreams, LLC
Lithonia, Georgia, United States
Enamel Lesions per BlueCheck
Number of enamel lesions counted after using BlueCheck
Time frame: Baseline, 4 weeks, and 12 weeks
Self-perceived reactions to BlueCheck application
Questionnaire clinician and subject feedback on the BlueCheck application
Time frame: Baseline, 4 weeks, and 12 weeks
Enamel Lesions per Xray
Number and location of visible enamel lesions on Xray
Time frame: Baseline, 4 weeks, and 12 weeks
Enamel lesions per intraoral camera
Number and location of enamel lesions detected by an intraoral camera using a caries mode
Time frame: Baseline, 4 weeks, and 12 weeks
White spots
Number and location of visible white spots per examiner's identification
Time frame: Baseline, 4 weeks, and 12 weeks
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