Diode Low-power Laser Before In-office Bleaching - Trial NCT05865275
Access comprehensive clinical trial information for NCT05865275 through Pure Global AI's free database. This phase not specified trial is sponsored by University of Campania Luigi Vanvitelli and is currently Completed. The study focuses on Tooth Sensitivity. Target enrollment is 30 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.
Study Focus
Sponsor & Location
University of Campania Luigi Vanvitelli
Timeline & Enrollment
N/A
Nov 09, 2021
Dec 20, 2022
Primary Outcome
baseline,Immediately,After 1 hour,After 24 hours,After 48 hours
Summary
Background: The aim of study was to investigate the effectiveness of low-level laser therapy
 (LLLT) use before in-office bleaching to prevent risk and intensity of tooth sensitivity.
 
 Methods: thirty patients were selected for this clinical trial. Before bleaching procedures
 with 38 % hydrogen peroxide, the participants were randomly divided into two groups of 15
 subjects. Test group: the patients teeth received a preliminary LLLT procedure by an 810 nm
 diode laser with 0.5 Watt for 30 s for an energy density of 15 J/cm2 and a group placebo: the
 patients received the same preliminary LLLT but with the device switch off. All patients were
 instructed to report their cold sensitivity experiences immediately, 1 h, 24 h, and 48 h
 after the end of bleaching by a visual analog scale score between 0-10.
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT05865275
Device Trial