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Orthodontic Appliance ComplicationNCT04604262

Does Use of the Waterpik Maintain Cleaner Teeth in Patients With Fixed Braces

A study testing Waterpik in people with Orthodontic Appliance Complication, run by York Teaching Hospitals NHS Foundation Trust at 1 site in United Kingdom.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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Trial summary

There is no long term evidence to show that the use of Waterpik® is effective for orthodontic patients with fixed braces. A Cochrane Systematic Review confirms this. The aims of this study is to find out if the use of Waterpik® in addition to the manual toothbrush is better to maintain clean teeth in patients with… Read more about this study

Who is it for?
Ages 8 to 60 years
Conditions the study is for
Orthodontic Appliance Complication
What is being tested?
Waterpik
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
34 participants
Where
1 siteUnited Kingdom
Study dates
1 Sep 2019to 26 Nov 2021
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 8 to 60 years
  • All sexes
  • No healthy volunteers
  • Child, Adult
  1. All patients will have a dental history that included brushing at least twice a day and be willing and able to comply with the trial regime. They will also be between 10 and 20 years of age and in good general health. Any patients with medical conditions and those necessitating chemotherapy which may alter the oral tissue's response to fixed appliance treatment will be excluded. Examples include heart conditions requiring antibiotic cover, diabetes mellitus, immunosuppressant drugs, antibiotics, steroids and hormonal therapy.
  2. Patients with decreased manual dexterity either due to mental or physical disabilities and poor compliance will be excluded. Patients with poor initial periodontal health will also be excluded.
  3. All medications which may alter plaque accumulation should be avoided during the trial period, but if required on professional advice should report this to the clinical investigator.
  4. All patients will have brackets as opposed to bands except permanent molar teeth which may be banded.
  5. The patients will have full upper and lower arch treatment as oppose to sectional arch treatment. This is so that the difficulties involved in cleaning all the teeth are similar.
  6. They should be bonded using one single type of cement, as we are unsure if different types of cement would influence the accumulation of plaque. This may be true with glass ionomer cement, as it has been shown to inhibit growth of some bacteria. The cement chosen for this purpose is Transbond XT® by 3M Unitek as this the cement most familiar to the operator. Furthermore any breakages from the appliances will be repaired using this cement. This will also ensure that consistent cement will be used.
  7. The fixed braces will be of the pre-adjusted Edgewise type as auxiliaries used in other appliance type may pose to be confounding factor. As this unit uses the AO Orthodontics, MBT prescription brackets, this will be the brackets used for this trial.
  8. Patients who already use any other supplements to the manual toothbrush for their oral hygiene will be excluded so as not to disadvantage their oral hygiene during their trial

Trial locations and contacts

1 site in 1 country.

United Kingdom1 site
  • York Teaching Hospital NHS Foundation Trust

    York, North Yorkshire, YO31 8HE

Other trials in United Kingdom

About this study

Official title: A Randomised Controlled Clinical Trial to Determine if the Use of the Waterpik in Addition to the Manual Toothbrush Maintains Cleaner Teeth in Patients With Fixed Braces

There is no long term evidence to show that the use of Waterpik® is effective for orthodontic patients with fixed braces. A Cochrane Systematic Review confirms this. The aims of this study is to find out if the use of Waterpik® in addition to the manual toothbrush is better to maintain clean teeth in patients with fixed braces. The null hypothesis is that there is no difference between patients using either Waterpik® in addition to the manual toothbrush (treatment group) when compared with patients using just the manual toothbrush (control group).

Read the detailed description

This will be a 56-week single blind, stratified; parallel group randomised controlled clinical trial. This will be a pseudo-longitudinal trial where observations are recorded at certain fixed intervals. The CONSORT guidelines for reporting randomised control trials will be followed. Examinations will be conducted at baseline, 8, 32 and 56 weeks with 56 weeks classified as the completion of treatment.

These are patients undergoing active orthodontic treatment involving full upper and lower arch fixed appliance therapy. As the selection criteria are quite complicated, a checklist will be used to ensure conformity.

Selection criteria:

  1. All patients will have a dental history that included brushing at least twice a day and be willing and able to comply with the trial regime. They will also be between 10 and 20 years of age and in good general health. Any patients with medical conditions and those necessitating chemotherapy which may alter the oral tissue's response to fixed appliance treatment will be excluded. Examples include heart conditions requiring antibiotic cover, diabetes mellitus, immunosuppressant drugs, antibiotics, steroids and hormonal therapy.
  2. Patients with decreased manual dexterity either due to mental or physical disabilities and poor compliance will be excluded. Patients with poor initial periodontal health will also be excluded.
  3. All medications which may alter plaque accumulation should be avoided during the trial period, but if required on professional advice should report this to the clinical investigator.
  4. All patients will have brackets as opposed to bands except permanent molar teeth which may be banded.
  5. The patients will have full upper and lower arch treatment as oppose to sectional arch treatment. This is so that the difficulties involved in cleaning all the teeth are similar.
  6. They should be bonded using one single type of cement, as we are unsure if different types of cement would influence the accumulation of plaque. This may be true with glass ionomer cement, as it has been shown to inhibit growth of some bacteria. The cement chosen for this purpose is Transbond XT® by 3M Unitek as this the cement most familiar to the operator. Furthermore any breakages from the appliances will be repaired using this cement. This will also ensure that consistent cement will be used.
  7. The fixed braces will be of the pre-adjusted Edgewise type as auxiliaries used in other appliance type may pose to be confounding factor. As this unit uses the AO Orthodontics, MBT prescription brackets, this will be the brackets used for this trial.
  8. Patients who already use any other supplements to the manual toothbrush for their oral hygiene will be excluded so as not to disadvantage their oral hygiene during their trial

The gold standard The Gold Standard for orthodontic patients is the use of manual toothbrushes to clean in the inter-bracket areas of the fixed braces after each meal or snack. However, for practical purposes, it may not be possible to do so. Some schools do not provide facilities for their pupils to clean their teeth except for the sinks in the toilet. Therefore, patients will be asked to clean their teeth after breakfast, tea and last thing at night. They will be asked to do so for two minutes each time. They will be asked to time themselves and to keep a diary. They will not be given a timer as this is not in keeping with a "real world" situation.

They will also be shown how to clean around the orthodontic brackets using a manual toothbrush by the dental nurse/hygienist using a model. To ensure conformity, this advice will be given by the same two/three dental nurse on each occasion. The dental nurse would be a qualified dental health educator and would be familiar with providing oral hygiene instruction to patients with fixed appliance therapy. However, no further oral hygiene instructions will be given throughout the duration of the trial.

Additionally, if they live in a non-fluoridated area, a 10 mls 2% Fluoride mouthwash would be advised. They would be advised to do this last thing at night by holding the mouthwash for one full minute and spitting out. They would be asked not to rinse thereafter and to go to bed. Since the North Yorkshire area is non-fluoridated, this advice would follow.

Each subject should be issued with a standard fluoride containing toothpaste, a manual toothbrush and those requiring, a Waterpik®. At each visit, they will be issued with replacement brushes or as recommended by the toothbrush manufacturers. As part of the agreement for the patient to take part, they will be given the fluoride mouth rinse to be used last thing at night. The use of any other oral hygiene implements will not be permitted throughout the duration of the trial. No other members of the family will be allowed to use the implements supplied for the purposes of this trial.

All subjects will be issued with a diary of their cleansing habits to encourage motivation and compliance. Only patients who showed good compliance at the preliminary discussion and instruction will be allowed to participate in the trial.

All the instructions will be reinforced by a printed handout.

Being tested
Waterpik

What participants receive

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

  • WaterpikDevice

    Waterpik dental water jet

Study groups in NCT04604262
Study groupRoleWhat they receive
Treatment GroupExperimentalWaterpik® in addition to the manual toothbrush
Receives: Device: Waterpik
ControlNo interventionManual toothbrush

What is being measured

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

  1. Change in Plaque index from baseline

    The patient will be disclosed by the clinical investigator who will be blind to the toothbrush group allocation. The disclosed mouth will be photographed and plaque scored at the same time. The photograph will allow for a re-score and to check the validity of the clinical score.

    Plaque will be assessed on the buccal surfaces of the teeth on which orthodontic brackets has been placed using the orthodontic modification of the Silness and Loe plaque index. This index has been shown to be sensitive in detecting differences in plaque levels in orthodontic patients with fixed braces. This index divides the tooth surface into four zones in relation to the orthodontic bracket: incisal, distal, mesial and cervical and codes 0-3 were assigned.

    Measured: 8, 32, 56 weeks

  2. Change in Gingivitis from baseline

    Gingivitis will be measured on the buccal surfaces of the teeth with the gingival index using a CPITN probe.

    Measured: 8, 32, 56 weeks

  3. Change in Gingival bleeding from baseline

    Gingival bleeding will be determined using the Eastman interdental bleeding index. This will involve inserting a wooden interdental cleaner (Interdental woodsticks, Oral-B Laboratories, Aylesbury, UK) between the teeth from the buccal aspect and depressing the interdental papilla by 1-2 mm. The presence or absence of marginal interdental bleeding from the papilla within 15 seconds will be recorded. The Eastman interdental bleeding index is the number of bleeding sites as expressed as a percentage of the total sites evaluated.

    Measured: 8, 32, 56 weeks

Timeline

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

  1. First posted27 Oct 2020
  2. Study start1 Sep 2019
  3. Primary completion26 Nov 2021
  4. Study completion26 Nov 2021

Why it stopped: Recruitment difficulties (due to Covid), no difference found between study arms

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
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Model description
This will be a 56-week single blind, stratified; parallel group randomised controlled clinical trial. This will be a pseudo-longitudinal trial where observations are recorded at certain fixed intervals.
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
34 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04604262
Sponsor's protocol ID
266235
Status last verified
Feb 2022
First submitted
9 Oct 2020
Last updated
24 Feb 2022
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Waterpik in people with Orthodontic Appliance Complication, run by York Teaching Hospitals NHS Foundation Trust at 1 site in United Kingdom.

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

Who may be eligible to take part?

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: stopped early, as of the sponsor's last update on 24 Feb 2022. 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 United Kingdom. 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 was stopped early (reason given: Recruitment difficulties (due to Covid), no difference found between study arms). Results are not available in the source record.

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?

Change in Plaque index from baseline (time frame: 8, 32, 56 weeks). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 24 Feb 2022.

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