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Plaque AccumulationNCT07469839

Water Flossing Versus Dental Floss for Oral Hygiene in Children Aged 10-15 Years: A Randomized Trial

A study testing Unflavored, unwaxed regular dental floss (Oral-B, USA) and Water flosser (Waterpik Cordless Plus Water Flosser, USA) in people with Plaque Accumulation, run by King Abdulaziz University at 1 site in Saudi Arabia.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The goal of this Randomized Clinical Trial is to compare the effectiveness of water flossing versus regular flossing in reducing dental plaque in children aged 10-15 years. The main question is the water flossing equal or more effective than regular flossing. Read more about this study

Who is it for?
Ages 10 to 15 yearsHealthy volunteers can take part
Conditions the study is for
Plaque Accumulation
What is being tested?
Unflavored, unwaxed regular dental floss (Oral-B, USA) and Water flosser (Waterpik Cordless Plus Water Flosser, USA)
Could I receive a placebo?
No, everyone receives an active treatment
How many people
55 participants
Where
1 siteSaudi Arabia
Study dates
1 Nov 2024to 30 Apr 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 10 to 15 years
  • All sexes
  • Healthy volunteers accepted
  • Child

Who may be able to join

  • The inclusion criteria included children aged 10-15 years, medically fit and systemically healthy, with no active orthodontic treatment or space maintainer with no use of any type of dental floss within the previous 24 hours.

Who cannot join

  • Children with fewer than four posterior proximal contacts were excluded from the study

Trial locations and contacts

1 site in 1 country.

Saudi Arabia1 site
  • King Abdulaziz University- Peditaric dentistry clinics

    Jeddah

Other trials in Saudi Arabia

About this study

Official title: The Effectiveness of Water Flossing Versus Regular Flossing for Oral Hygiene in Children Aged 10-15 Years: A Randomized Clinical Trial

The goal of this Randomized Clinical Trial is to compare the effectiveness of water flossing versus regular flossing in reducing dental plaque in children aged 10-15 years. The main question is the water flossing equal or more effective than regular flossing. Each participant will use both interdental cleaning methods, water flossing and regular flossing, in two separate visits and the plaque Index (PI) will be recorded.

Regular Dental Floss Group: Unflavored, unwaxed regular dental floss (Oral-B, USA), or Water Flosser: Water flosser (Waterpik Cordless Plus Water Flosser, USA)

Read the detailed description

Ethical Approval:

The study protocol was reviewed and approved by the Research Ethics Committee of the Faculty of Dentistry, King Abdulaziz University, Jeddah, Saudi Arabia. Written informed consent was obtained from all parents or legal guardians prior to participation, in accordance with the Declaration of Helsinki.

Study Design:

This study was designed as a randomized, controlled crossover clinical trial. Each participant used both interdental cleaning methods, water flossing and regular flossing, in two separate visits with a 14-day washout period between interventions to minimize carryover effects.

Study Setting:

The study was conducted at the College of Dentistry and the University Dental Hospital, King Abdulaziz University, Jeddah, Saudi Arabia.

Sample Selection:

Participants were recruited using a convenience sampling approach from patients attending the College of Dentistry and the University Dental Hospital at King Abdulaziz University. Eligible participants who met the inclusion criteria were enrolled after obtaining informed parental consent.

Randomization (Sequence Generation) Random allocation sequences were generated using an online randomization tool (https://www.randomizer.org). Two sets of random numbers were created, corresponding to the two intervention orders.

Allocation Concealment:

Each allocation code was printed, cut into identical slips, and sealed in opaque envelopes. The envelopes were placed in a single container. Upon recruitment, each participant selected one envelope to determine their assigned intervention sequence.

Blinding:

Due to the nature of the interventions, blinding of the participants and operators was not feasible. However, the statistician responsible for data analysis was blinded to the group assignments to minimize analytical bias.

Inclusion and Exclusion Criteria:

The inclusion criteria included children aged 10-15 years, medically fit and systemically healthy, with no active orthodontic treatment or space maintainer with no use of any type of dental floss within the previous 24 hours. Children with fewer than four posterior proximal contacts were excluded from the study.

Sample Size Calculation:

The sample size was calculated using G*Power software (version 3.1.9.7), based on the findings of a previous study who compared the efficacy of water flossers and regular floss in plaque removal. Assuming a power of 80%, a two-tailed significance level (α) of 0.05, and an effect size derived from the cited study, a total of 44 participants (22 per group) were required to achieve sufficient statistical power.

Study Procedures:

Participants were screened according to the inclusion and exclusion criteria. Parents were informed that participation was voluntary and that all collected data would remain confidential and accessible only to the research team.

Each participant was randomly assigned to start with one of the following:

  • Regular Dental Floss: Unflavored, unwaxed regular dental floss (Oral-B, USA), or
  • Water Flosser Group: Water flosser (Waterpik Cordless Plus Water Flosser, USA).
  • both are FDA-regulated medical devices (Class I). After the first visit, a 14-day washout period was observed before the crossover intervention was applied.

At the first visit, demographic data (participant initials, age, and sex) and group allocation were recorded. A clinical examination was performed to assess the Plaque Index (PI). All participants received standardized oral hygiene instructions, including brushing twice daily with the Modified Bass Technique using a soft-bristled toothbrush and fluoridated toothpaste. Participants received instructions on the proper use of the assigned interdental cleaning method and performed the procedure independently.

The Plaque Index (PI) was recorded for all teeth according to the following criteria:

  • 0: No plaque in the gingival area.
  • 1: A film of plaque adhering to the free gingival margin and adjacent tooth area, detectable only by a probe.
  • 2: Moderate accumulation of soft deposits visible to the naked eye within the gingival margin.
  • 3: Abundant soft matter within the gingival pocket and/or along the gingival margin.

At the second visit, participants switched to the opposite cleaning method (water flosser or regular floss), and plaque scores were reassessed using the same PI criteria.

Being tested
Unflavored, unwaxed regular dental floss (Oral-B, USA), Water flosser (Waterpik Cordless Plus Water Flosser, USA)
Keywords
Water flossing, pediatric dentistry, randomized clinical trial, dental plaque, oral hygiene, regular flossing
Medical subject headings
Dental Plaque

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Unflavored, unwaxed regular dental floss (Oral-B, USA)Device

    Also called Group A

    Plaque removal

  • Water flosser (Waterpik Cordless Plus Water Flosser, USA)Device

    Plaque removal

Study groups in NCT07469839
Study groupRoleWhat they receive
Regular Dental FlossExperimentalUnflavored, unwaxed regular dental floss (Oral-B, USA)
Receives: Device: Unflavored, unwaxed regular dental floss (Oral-B, USA); Device: Water flosser (Waterpik Cordless Plus Water Flosser, USA)
Water FlosserExperimentalWater flosser (Cordless Plus Water Flosser, USA)
Receives: Device: Unflavored, unwaxed regular dental floss (Oral-B, USA); Device: Water flosser (Waterpik Cordless Plus Water Flosser, USA)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Plaque Index (PI)

    to assess the Plaque Index (PI) using the criteria of Silness and Löe (1964).

    Measured: 16 days, 1st visit followed by 14 days washout period then 2nd visit

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted13 Mar 2026
  2. Study start1 Nov 2024
  3. Primary completion30 Apr 2025
  4. Study completion30 Apr 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Crossover
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
55 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07469839
Sponsor's protocol ID
169-11-24
Status last verified
Mar 2026
First submitted
26 Feb 2026
Last updated
18 Mar 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Due to privacy

Publications

  • Abdellatif H, Alnaeimi N, Alruwais H, Aldajan R, Hebbal MI. Comparison between water flosser and regular floss in the efficacy of plaque removal in patients after single use. Saudi Dent J. 2021 Jul;33(5):256-259. doi: 10.1016/j.sdentj.2021.03.005. Epub 2021 Mar 31.

    PubMed 34194188

Questions about this trial

What is this clinical trial studying?

A study testing Unflavored, unwaxed regular dental floss (Oral-B, USA) and Water flosser (Waterpik Cordless Plus Water Flosser, USA) in people with Plaque Accumulation, run by King Abdulaziz University at 1 site in Saudi Arabia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 18 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Saudi Arabia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Plaque Index (PI) (time frame: 16 days, 1st visit followed by 14 days washout period then 2nd visit). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07469839, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Mar 2026.

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