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Clinical Trial Summary

Compare by clinical observation, photographs and fluorescence the efficacy of sodium fluoride, silanofluoride and thiefenfluoride in treating white spots.


Clinical Trial Description

This in vivo study will be a randomized experimental clinical trial to be carried out in the Department of Pediatric Dentistry of the International University of Catalonia. Patients between the ages of 3 and 12, who attend the dental university clinic of the International University of Catalonia, will be part of the study. Parents or legal guardians will be informed of the treatment procedure with a patient information sheet and informed consent will be given. Once signed, the patient will be assigned to one of the 3 study groups. Accepting an alpha risk of 5% and with a power of 80% in a bilateral contrast, 15 subjects in each group are required to detect a minimum difference of 4 points between two groups, assuming that there are 3 groups and a standard deviation of 4.9. a follow- up loss rate of 10% has been estimated. The total number of children will be 45 by 15 for each group. In order to analyze the degree of agreement of one examiner, 15 children will be evaluated twice, with a separation of one month. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04705428
Study type Interventional
Source Universitat Internacional de Catalunya
Contact
Status Completed
Phase N/A
Start date January 1, 2021
Completion date June 30, 2022

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