Clinical Study to Evaluate of The Whitening Efficacy and Safety of REMEWHITE

JDC Tech70 enrolled

Overview

The purpose of this study is to determine the effect of REMEWHITE on tooth whitening.

This study intended to establish the efficacy of REMEWHITE after using the product under controlled conditions at the hospital. The efficacy of the product was assessed at the end of the study; clinical examination by the dentist.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

Conditions

Tooth Whitening

Interventions

Hydrogen PeroxideDRUG

Whitening product syringe type

Eligibility

Sex: ALLMin age: 20 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * ability to understand and provide informed consent * general good health male and female adults, were 20 years or older * no pregnant woman * had six caines-free maxillary anterior teeth without restorations on the labial surfaces Exclusion Criteria: * had severe internal discoloration (tetracycline stains, fluorosis, pulpless teeth) * evidence of fracture or major cracks on tooth * were pregnant or nursing * had tooth sensitivity * smokers * had teeth shade A1, A2

Locations (1)

The cathiloc university of korea seoul st. mary's hospital

Seoul, South Korea

Outcomes

Primary Outcomes

colorimeter

Time frame: 12 weeks after treatment

Secondary Outcomes

colorimeter

Time frame: 24 weeks after treatment

Data from ClinicalTrials.gov

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