Adjunctive Oral Hygiene Aids in Reducing Oral Hygiene Parameters Among Orthodontic Patients
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Water flosser and super flosser, Orthodontic brush.
- Who it may be relevant to
- Registry conditions: Gingival Bleeding, Dental Plaque Accumulation. Basic parameters: 18 years — 35 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United Arab Emirates
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Adjunctive Oral Hygiene Aids in Reducing Commonly Seen Oral Hygiene Parameters Among Orthodontic Patients: a Randomized Controlled Trial
Overview
Adult orthodontic patients aged 18-30 were included in a randomised, singleblind clinical research using a split-mouth design at a dental clinic. Both theWaterflosser® and the Super-Floss® water flossers are manufactured by Oral-B.
Detailed description
In order to reduce gingival inflammation and remove subgingival plaque, oral hygiene therapy is necessary. The available evidence indicates that mechanical plaque control, which patients administer themselves daily, is the most important factor in managing and reducing plaque accumulation. Aim: This research aimed to determine whether Waterflosser or Superfloss was more effective in lowering the gingival bleeding score and plaque. Methods: Adult orthodontic patients aged 18-30 were included in a randomised, single-blind clinical research using a split-mouth design at a dental clinic. Both the Waterflosser® and the Super-Floss® water flossers are manufactured by Oral- B.
Interventions
- Device Water flosser and super flosser
Participant will use in one area superfloss and the other area waterfloss - Device Orthodontic brush
Participant will use orthodontic brush to brush in the upper/lower quadrant
Primary outcome measures
- Number of Participants with Gingival Bleeding [Time frame: Through study completion, an average of 1 month]
Secondary outcome measures (1)
- Number of Participants with Dental Plaque [Time frame: Through study completion, an average of 1 month]
Eligibility criteria
Inclusion criteria
- Participants aged 18-35 years undergoing orthodontic treatment and
- systemically healthy without habits
Exclusion criteria
- Participants not undergoing orthodontic treatment and participants undergoing orthodontic treatment in the included age category but with systemic conditions prevalent
- missing teeth and
- treated previously for periodontal conditions
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Non-randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Prevention
Study locations
United Arab Emirates · 1 center
- Ajman university — Ajman
Identifiers
NCT: NCT06779279 · D-F-H-17-Dec