Evaluation of In-office Bleaching-induced Sensitivity With 2 or 7 Days Interval Between Sessions - Trial NCT06394557
Access comprehensive clinical trial information for NCT06394557 through Pure Global AI's free database. This phase not specified trial is sponsored by Universidade Federal Fluminense and is currently Recruitment Completed. The study focuses on Tooth Sensitivity. Target enrollment is 47 participants.
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Study Focus
Sponsor & Location
Universidade Federal Fluminense
Timeline & Enrollment
N/A
Aug 14, 2023
Jul 01, 2024
Primary Outcome
Tooth sensitivity,Tooth sensitivity,Tooth sensitivity
Summary
Clinical randomized single-blind trial, used to measure the level of tooth sensitivity (TS)
 after in-office dental bleaching sessions, on volunteers using a modified visual analog scale
 (VAS). We selected for this study, 47 patients with color 2M2 or darker (Using 0M1 - 5M3 Vita
 bleaching shade guide). We performed two bleaching sessions with an acidic 35% hydrogen
 peroxide gel with either a 1-week or 2-day interval. We recorded the TS up to 48 h with a VAS
 scale and the color at baseline and 30 days after bleaching with a value-oriented shade guide
 and a spectrophotometer. The risk and intensity of TS and the color change were compared
 between the two groups.
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT06394557
Non-Device Trial