drugset / Trial / NCT02603354

Efectiveness of a Brief Protocol by a Low (6%) Concentration Gel Peroxide Hydrogen of Teeth Bleaching

NCT02603354

Completed 31 enrolled University of Chile
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this clinical study was to evaluate, the effectiveness and sensitivity post-treatment of a 6% hydrogen peroxide with nitrogen-doped titanium dioxide light activated bleaching agent, the impact of shorter interval times on tooth sensitivity and to compare the efficacy with 2 different application protocols. This is a clinical randomized double-blind split-mouth study. 31 patients were treated with: one upper hemi arcade with one application of 36 minutes and the other hemi arcade with 3 applications of 12 minutes each with a 6% hydrogen peroxide. Two sessions were appointed with 48h of intervals between them. Tooth colour was registered by VITA Classical amd VITA Bleach guide by two blinded assessors in the beginning, immediately after each session. Tooth colour variation and sensitivity were compared between both application protocols

Timeline

Start
2015-03
Primary completion
2015-04
Completion
2015-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Hydrogen Peroxide Small molecule 6 % Topical

Indications