Skip to content

Adjunctive Oral Hygiene Aids in Reducing Oral Hygiene Parameters Among Orthodontic Patients

Adjunctive Oral Hygiene Aids in Reducing Commonly Seen Oral Hygiene Parameters Among Orthodontic Patients: a Randomized Controlled Trial

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06779279
Acronym
D-F-H-17-Dec
Enrollment
102
Registered
2025-01-16
Start date
2025-02-10
Completion date
2025-03-26
Last updated
2025-01-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dental Plaque Accumulation, Gingival Bleeding

Keywords

waterflosser, superfloss, gingival bleeding, Dental Plaque

Brief summary

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

DEVICEWater flosser and super flosser

Participant will use in one area superfloss and the other area waterfloss

DEVICEOrthodontic brush

Participant will use orthodontic brush to brush in the upper/lower quadrant

Sponsors

sudhir rama varma
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Masking description

No masking done

Intervention model description

The study comprised 18-35-year-old girls and boys planning orthodontic treatment. Participants had upper right tooth to lower left molar braces, a pocket depth of 3 mm, and had not flossed in 24 hours. Smoking, periodontal disease, missing teeth, voids between teeth in the arch, and systemic disorders disqualified participants.

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
Number of Participants with Gingival BleedingThrough study completion, an average of 1 monthGingival bleeding scores will be evaluted 0-no gingival bleeding 1. mild gingival bleeding 2. moderate gingival bleeding 3. spontaneous gingival bleeding

Secondary

MeasureTime frameDescription
Number of Participants with Dental PlaqueThrough study completion, an average of 1 monthDental Plaque scores will be evaluated 0-No dental plaque 1. Upto 1/3rd of the tooth surface 2. more than 1/3rd and less than 2/3rd of tooth surface 3. more than 2/3rd of tooth surface

Countries

United Arab Emirates

Contacts

Primary ContactSudhir Rama Varma, MDS
s.varma@ajman.ac.ae971506595075

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026