Three Different Oral Hygiene Regimes on Three Volatile Sulfur Compounds

February 18, 2016 updated by: Ei Ei Aung, Tokyo Medical and Dental University
The purpose of the study is to evaluate the effect of various oral hygiene regimes on three volatile sulfur compounds.

Study Overview

Status

Completed

Conditions

Detailed Description

Thirty male monk volunteers who matched with the including criteria were divided randomly into two groups. Both groups were practiced to brush their teeth with scrubbing method for one week. Then, each group were instructed to do different additional protocol regimen- group A have to do mouth washing and tooth brushing and group B have to practice tongue cleaning addition to tooth brushing for three weeks. At the fifth week, both groups were instructed to practice tooth brushing, mouth washing and tongue cleaning. Three different volatile sulfur compounds were measured by oral chroma. Tongue characteristics, oral examination were checked as the outcomes of this study.

Study Type

Interventional

Enrollment (Actual)

30

Phase

  • Phase 4

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 30 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

Description

Inclusion Criteria:

  • Clinical diagnosis of oral malodor
  • No systemic diseases and no severe dental diseases
  • At least 20 functional teeth

Exclusion Criteria:

  • Risky oral habit (smoking and betel quid chewing)
  • Current use of antibiotics or any drugs
  • Current use of any kind of mouthwash

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: group A
Mouthwash (chlorine dioxide 12ml two times per day, for three weeks)
First week, subjects were instructed to do regular tooth brushing. After that group A was requested to use chlorine dioxide mouthwash two time per days for three weeks in addition to tooth brushing and then, one week for combination of tooth brushing, tongue cleaning and mouth washing.
Other: group B
Small toothbrush for tongue cleaning two times per day for three weeks
First week, subjects were instructed to do regular tooth brushing. After that group B was requested to brush their tongue with small toothbrush two time per days for three weeks in addition to tooth brushing and then, one week for combination of tooth brushing, tongue cleaning and mouth washing.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Three different volatile sulfur compounds
Time Frame: up to 5weeks
Investigator measured three different volatile sulfur compounds: hydrogen sulfide, methyl mercaptan, dimethyl sulfide concentrations (ng/10ml) by using Oral chroma.
up to 5weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Oral Health examination
Time Frame: up to 5weeks
As oral examination, investigator examined present teeth, DMF-T (decayed, missing and filled teeth)
up to 5weeks
Tongue coating characteristics
Time Frame: up to 5weeks
As tongue coating characteristics, investigator examined tongue coating score (by using winkle tongue coating index) at the baseline, one week later, four weeks later and five weeks later.
up to 5weeks
Number of teeth with bleeding on probing
Time Frame: up to 5weeks
up to 5weeks
Plaque index score
Time Frame: up to 5weeks
up to 5weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

September 1, 2013

Primary Completion (Actual)

October 1, 2013

Study Completion (Actual)

November 1, 2013

Study Registration Dates

First Submitted

February 8, 2016

First Submitted That Met QC Criteria

February 18, 2016

First Posted (Estimate)

February 23, 2016

Study Record Updates

Last Update Posted (Estimate)

February 23, 2016

Last Update Submitted That Met QC Criteria

February 18, 2016

Last Verified

February 1, 2016

More Information

Terms related to this study

Other Study ID Numbers

  • OHP-018-EI-2

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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