EFFECTIVENESS of WATER FLOSS in PLAQUE REMOVAL and PREVENTION of WHITE SPOT LESIONS in ORTHODONTIC PATIENTS: a RANDOMISED CONTROLLED CLINICAL TRIAL (WATER FLOSS)

December 20, 2024 updated by: Dr Afif Shafie bin Abd Samad, University of Malaya

This clinical trial aims to learn if water floss is as efficient as other interdental cleaning tools and can prevent plaque accumulation and white spot lesions (WSLs) in orthodontic patients. It will also assess the impact of water floss on gingival health. The main questions it aims to answer are:

  • Which interdental cleaning tools reduce plaque accumulation and improve gingival health in orthodontic patients?
  • Which interdental cleaning tools lower the incidence of white spot lesions compared to conventional oral hygiene practices? Researchers will compare the oral health of Orthodontic patients' using different interdental cleaning tools to evaluate their effectiveness in improving oral health outcomes.

Participants will:

  • Be assigned to one of two groups:

    • Intervention group: instructed to use water flossing in their oral hygiene routine.
    • Control group: instructed to use dental floss and interdental brush in their oral hygiene routine.
  • Participate for 8 months, with clinical assessments for plaque and gingival health and photographic documentation for WSLs at baseline (T0), and at 2-month intervals (T1, T2, T3, and T4).

Study Overview

Status

Active, not recruiting

Conditions

Intervention / Treatment

Detailed Description

This clinical trial aims to learn if water floss is as efficient as other interdental cleaning tools and can prevent plaque accumulation and white spot lesions (WSLs) in orthodontic patients. It will also assess the impact of water floss on gingival health. The main questions it aims to answer are:

  • Which interdental cleaning tools reduce plaque accumulation and improve gingival health in orthodontic patients?
  • Which interdental cleaning tools lower the incidence of white spot lesions compared to conventional oral hygiene practices? Researchers will compare the oral health of Orthodontic patients' using different interdental cleaning tools to evaluate their effectiveness in improving oral health outcomes.

Participants will:

  • Be assigned to one of two groups:

    • Intervention group: instructed to use water flossing in their oral hygiene routine.
    • Control group: instructed to use dental floss and interdental brush in their oral hygiene routine.
  • Participate for 8 months, with clinical assessments for plaque and gingival health and photographic documentation for WSLs at baseline (T0), and at 2-month intervals (T1, T2, T3, and T4).

Aim of the study:

To evaluate the effectiveness of Water Floss in plaque removal and preventing WSLs among orthodontic patients.

Primary Objectives

  1. To measure the effectiveness of the water floss in plaque removal based on the Oral Plaque Index (OPI) among fixed appliance patients at T0, T1, T2, T3, and T4.
  2. To measure the effectiveness of water flosser based on the incidence of White Spot Lesions (WSLs) among fixed appliance patients at 0 months (T0), 3 months (T1), 6 months (T2), 9 months (T3), and 12 months (T4).
  3. To compare the incidence of WSLs between conventional interdental cleaning tools with water floss among fixed appliance patients at T0, T1, T2, T3, and T4.
  4. To see the correlation of oral plaque index (OPI) and WSLs between conventional interdental cleaning tools with water floss among fixed appliance patients at T0, T1, T2, T3, and T4.

Secondary Objectives

  1. To see the effect of conventional interdental cleaning tools with water floss among fixed appliance patients on gingival health at T1, T2, T3 and T4.
  2. To explore patients' perception of the usage of water flossers using self- administered questionnaires measured at T1 and T4.

Study design/Trial Design

The study will be designed based on the guidelines from the Consolidated Standards of Reporting Trials (CONSORT) statement and will be registered in Clinicaltrials.gov. All methods will be performed according to the relevant guidelines and regulations. The study was conducted according to the Declaration of Helsinki (as revised in 2013).

The study will be conducted in three phases:

i. Calibration of Orthodontic Plaque Index (OPI), Gingival Index (GI) and Enamel Decalcification Index (EDI) ii. Questionnaire translation and validation iii. Intervention: Baseline (T0, 0 months) and post-intervention (T1-T4, 3 to 12 months) The intervention study is a single-side blinded, two-arm parallel, prospective, single- centre randomised clinical trial. The study will be conducted from April 2024 to October 2025 in the Orthodontic Postgraduate Clinic, Universiti Malaya.

Participants

Participants will be recruited voluntarily based on inclusion and exclusion criteria; the centre would be located at the Orthodontic Postgraduate Clinic of Universiti Malaya. Informed and written consent will be obtained from the participants after the research procedure, and the research risks and benefits explained.

Inclusion and exclusion criteria:

Inclusion Criteria:

Mild to moderate crowding upper and lower arch 18 years old and above Patients with BPE score 0/1 Stay in areas with the same concentration of water fluoridation No history of orthodontic treatment before Able to read and understand in English or Bahasa Melayu Fit and healthy

Exclusion Criteria:

Severe crowding Less than 18 years old Patients with BPE score more than 2 Patients with systemic disease and syndromic Syndromic patients (eg; Cleft lip and palate) Unable to read and understand in English or Bahasa Melayu Clinically missing teeth (impacted/congenitally missing) Patients with upper and lower fixed appliance Patients with segmental fixed appliances in single or both arches.

Intervention In this research study, we would like to investigate incorporating water flossing into the oral hygiene routine, comparing it with oral hygiene practices with conventional interdental cleaning tools (Interdental brush and dental floss). The study design involves two groups: the intervention group, which will integrate water flossing into their daily oral care regimen, and the control group, which will adhere to their usual oral hygiene practices with conventional interdental cleaning tools.

Outcomes The study's outcomes will evaluate the presence and severity of white spot lesions through the Enamel Decalcification Index (EDI). Plaque accumulation will be assessed by employing the Orthodontic Plaque Index (OPI). Gingival health by using Gingival Index. A comprehensive questionnaire will be administered to determine the perceptions of interdental cleaning devices.

At Pre-Intervention (T0) : Full mouth scaling will be done and all study samples will be bonded with a straight-wire fixed appliance by the same bracket system McLaughlin, Bennett, and Trevisi (MBT) bracket system 022 x028 slot. Post-bond-up and diet instructions will be given to every participant.

Baseline data will be collected:

I.Orthodontic Plaque Index (OPI) Score 2.Gingival Index 3.Enamel decalcification index (EDI) score

Protocol for Orthodontic Plaque Index (OPI) data collection. The Orthodontic Plaque Index (OPI) will be conducted using a blunt probe with the scraping technique on the labial surfaces of teeth located mesial to the 6s. A disclosing tablet will not be utilised in this study due to its potential impact on the appearance of white spot lesions (WSLs).

Protocol for Gingival index A value is assigned to three tooth surfaces: vestibular, mesial, and distal. Lingual surfaces won't be included in our study. The periodontal probe is used with light pressure on the gingival sulcus to evaluate the bleeding. The assigned score to every surface is between 0 and 3 and it defines the level of gingival inflammation.

Protocol for Enamel Decalcification Index (EDI) data collection After the gingival assessment, the archwire and auxiliaries will be removed. Tooth surfaces will be cleaned using a slow-speed bristle brush without pumice, and the teeth will be dried before taking the intraoral images.

The primary investigator (ASAS) will take an intraoral clinical photo using a Canon EOS RP camera with an aperture of f/25, a shutter speed of 1/125, and an ISO of 500. A Godox ML-150 macro ring flash set at maximum intensity will be used for illumination. The images will be cropped and arranged using Canva.The Enamel Decalcification Index (EDI) representing the white spot lesions will be scored based on the Enamel Decalcification Index by (Banks & Richmond, 1994).

Study Type

Interventional

Enrollment (Actual)

32

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Malaysia
      • Kuala Lumpur, Malaysia, 50603
        • Faculty of Dentistry, Universiti Malaya, Kuala Lumpur, Kuala Lumpur 50603

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

Mild to moderate crowding upper and lower arch 18 years old and above Patients with BPE score 0/1 Stay in areas with the same concentration of water fluoridation No history of orthodontic treatment before Able to read and understand in English or Bahasa Melayu Fit and healthy Patients with upper and lower fixed appliance

Exclusion Criteria:

Severe crowding Less than 18 years old Patients with BPE score more than 2 Patients with systemic disease and syndromic Syndromic patients (eg; Cleft lip and palate) Unable to read and understand in English or Bahasa Melayu Clinically missing teeth (impacted/congenitally missing) Patients with segmental fixed appliances in single or both arches.

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: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Groups of orthodontic patients with experimental interdental cleaning tools ( Water Flosser )
Groups of orthodontic patients with Water Flosser
Device: water flosser
A water flosser will be provided for use throughout the study, with participants instructed to use it once daily, specifically at the end of the day before bedtime.
No Intervention: Groups of orthodontic patients with controlled interdental cleaning tools
Groups of orthodontic patients with controlled interdental cleaning tools ( dental floss and interdental brush)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
White spot lesion
Time Frame: From enrollment to the end of study at 8 months
White spot lesion assessment using the Enamel Decalcification Index (EDI) by observing the clinical photos
From enrollment to the end of study at 8 months
Dental plaque
Time Frame: From enrollment to the end of study at 8 months
Dental plaque using the Orthodontic Plaque Index (OPI)
From enrollment to the end of study at 8 months
Gingival health
Time Frame: From enrollment to the end of study at 8 months
Gingival health assessment using the gingival index
From enrollment to the end of study at 8 months

Collaborators and Investigators

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

Sponsor

University of Malaya

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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 (Actual)

April 1, 2024

Primary Completion (Estimated)

October 31, 2025

Study Completion (Estimated)

October 1, 2026

Study Registration Dates

First Submitted

December 20, 2024

First Submitted That Met QC Criteria

December 20, 2024

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

December 20, 2024

Last Verified

April 1, 2024

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • DF CD 2424/0060 (P)
  • UMG052E-2024 (Other Grant/Funding Number: UNIVERSITI MALAYA)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

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.

Clinical Trials on Dental Plaque

Clinical Trials on water flosser

Search Similar Trials

Sponsors and Collaborators

Medical Conditions

Drug Interventions

CROs by country

CROs in Austria

Conditions

Rare Diseases

Drug Interventions

Dietary Supplements

Sponsor/Collaborators

Locations

Subscribe