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The Efficacy and Safety of Tooth Bleaching Procedure Using Y10 Whitening Toothpaste and RF Current

NCT02841514 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2019-07-10

No results posted yet for this study

Summary

Study title: The Efficacy and Safety of tooth bleaching procedure using Y10 Whitening toothpaste and RF current

The Device: The Brighttonix Y10 Tooth Whitening system is indicated for use in painless non-invasive tooth whitening treatments.

Design: Single center, randomized, controlled, double blind, two-arm, prospective clinical study.

Follow up visits at 7 days (phone visit), 12 weeks and 26 weeks.

Conditions

  • Tooth Bleaching

Interventions

DEVICE

The Y10 Tooth Whitening system including the Y10 toothpaste and the Y10 device

OTHER

OTC toothpaste and an unoperated Y10 device

Sponsors & Collaborators

  • Brighttonix Medical Ltd.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-09-30
Primary Completion
2017-04-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02841514 on ClinicalTrials.gov