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Braces wearers: new study reveals best mouthwash for cleaner teeth

NCT ID NCT07490873

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jul 08, 2026 · Updated 2 times

Summary

This study tests three different mouthwashes (chlorhexidine, cetylpyridinium chloride, and essential oil) in 24 people with braces to see which one reduces plaque and gum inflammation best. Participants will try each mouthwash for a week, with breaks in between. The goal is to find the most effective and patient-friendly option for keeping teeth and gums healthy during orthodontic treatment.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

20 people

The number who actually took part.

Started

Jan 2026

Finished

Jul 2026

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

14 to 30 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Age 14-30 years. * Wearing orthometric-type fixed orthodontic appliances(metallic brackets and archwires) and currently in alignment stage. * Able and willing to attend all study visits and comply with study procedures, including washout periods and mouthwash use. * Baseline oral status after preparatory phase: plaque index (Löe \& Silness) ≥ 1.0 and gingival index (Löe \& Silness) ≥ 0.5. * BOP less than 10%. * Systemically healthy individuals with no history of antibiotic use or other medications in the preceding 3 months. * Willing to refrain from using any other mouthwash or antimicrobial oral hygiene product (except for the assigned study mouthwash and their routine toothpaste) throughout the study. * Provide written informed consent (and parental/guardian consent if under legal age). Exclusion Criteria: * Periodontitis patients and untreated caries requiring urgent care. * Smoking or use of tobacoo/nicotine products(including vaping). * Known allergy or hypersensitivity to CHX, CPC, EO components (thymol, eucalyptol, menthol, methyl salicylate), or any ingredient in the study formulations. * Pregnancy or breastfeeding. * Use of any antiseptic mouthwash, oral probiotic, or antimicrobial gel in the 3 months prior to baseline.

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • College of Dentistry, University of Baghdad

    Baghdad, Baghdad Governorate, Iraq