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.
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)
- Type of treatment
- Pill or oral medicine, Medical device
- 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
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.
- Conditions
- Plaque Accumulation
- 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 group | Role | What they receive |
|---|---|---|
| Regular Dental Floss | Experimental | Unflavored, 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 Flosser | Experimental | Water 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.
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.
- First posted13 Mar 2026
- Study start1 Nov 2024
- Primary completion30 Apr 2025
- Study completion30 Apr 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Plaque AccumulationStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- King Abdulaziz University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Shahad Abudawood, King Abdulaziz University
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
Study at a glance
From the registry record, last updated by the sponsor on 18 Mar 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effectiveness of Water Flossing Versus Regular Flossing for Oral Hygiene in Children Aged 10-15 Years: A Randomized Clinical Trial
- ClinicalTrials.gov ID
- NCT07469839
- Acronym / sponsor ID
- 169-11-24
- Conditions
- Plaque Accumulation
- Keywords
- Water flossing, pediatric dentistry, randomized clinical trial, dental plaque, oral hygiene, regular flossing
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 55 participants (actual)
- Lead sponsor
- King Abdulaziz UniversityUniversity, hospital or other
- Study start
- 1 Nov 2024 (actual)
- Primary completion
- 30 Apr 2025 (actual)
- Study completion
- 30 Apr 2025 (actual)
- First posted
- 13 Mar 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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)
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.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Regular Dental Floss | Experimental | Device: Unflavored, unwaxed regular dental floss (Oral-B, USA), Device: Water flosser (Waterpik Cordless Plus Water Flosser, USA)Unflavored, unwaxed regular dental floss (Oral-B, USA) |
| Water Flosser | Experimental | Device: Unflavored, unwaxed regular dental floss (Oral-B, USA), Device: Water flosser (Waterpik Cordless Plus Water Flosser, USA)Water flosser (Cordless Plus Water Flosser, USA) |
Who may qualify
- Ages
- 10 to 15 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child
Key inclusion criteria (1 listed)
- 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.
Key exclusion criteria (1 listed)
- Children with fewer than four posterior proximal contacts were excluded from the study
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Unflavored, unwaxed regular dental floss (Oral-B, USA)Also: Group APlaque removal | Device | Regular Dental Floss, Water Flosser |
| Water flosser (Waterpik Cordless Plus Water Flosser, USA)Plaque removal | Device | Regular Dental Floss, Water Flosser |
Primary outcome
Plaque Index (PI)
Time frame: 16 days, 1st visit followed by 14 days washout period then 2nd visit
to assess the Plaque Index (PI) using the criteria of Silness and Löe (1964).
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 18 Mar 2026.
- Results publication: PubMed 34194188Abdellatif 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.
- Individual participant dataSharing planned: No. Due to privacy
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
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.