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Clinical Trials/NCT07240428
NCT07240428CompletedNot Applicable

Comparison Between Interdental Brush and Water Floss on Plaque Accumulation and Gingival Inflammation in Patients Undergoing Fixed Orthodontic Treatment: A Single Blinded Split-Mouth Randomized Controlled Clinical Trial

King Abdullah University Hospital1 site in 1 country75 target enrollmentStarted: July 1, 2024Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
75
Locations
1
Primary Endpoint
Plaque Index

Study Overview

Brief Summary

The goal of this clinical trial is to test the ability of water flosser to remove plaque and reduce gingival inflammation in patients undergoing fixed orthodontic treatment.

The main questions it aims to answer are:

Does water flosser remove plaque effectively in orthodontic patients? Does water flosser reduce gum inflammation in orthodontic patients?

Researchers compared water flosser to interdental brush to see if there is a difference in plaque and inflammation reduction.

Participants used interdental brush to clean between their teeth and around brackets in one side of their mouth, and they used water flosser to clean between the teeth and around brackets in the other side. The study lasted for 3 months.

Detailed Description

  • Study design This is a randomized controlled single blinded clinical trial, with split mouth design.
  • Sample size Forty seven subjects with fixed orthodontic appliance were recruited from patients attending dental teaching clinics at Jordan University of Science and Technology. The age range was between 18 and 35 years. They were randomly assigned to use interdental brush on one side of the mouth, and water floss on the other side in a split mouth design.

The study lasted for 3 months.

  1. Inclusion criteria:

1. Patients with fixed orthodontic appliance in the upper and lower arches. 2. Patients with healthy gingiva with no periodontal disease. 3. Patient's orthodontic plan doesn't require extraction of any teeth during the study period. .

4. Patients should have at least 26 teeth. 5. Patients are motivated and able to clean their teeth. 6. Patients should not have caries, overhang restorations, crowns, bridges or implants 7. Adults 18-35 years old. 2. Exclusion criteria:

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Double (Investigator, Outcomes Assessor)

Masking Description

patients know what they're using, but examiner measuring plaque/gingival index is blinded

Eligibility Criteria

Ages
18 Years to 35 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Patients with fixed orthodontic appliance upper and lower arches.
  • •Patients with healthy gingiva with no periodontal disease.
  • •Patient's orthodontic plan doesn't require extraction of any teeth during the study period.
  • •Patients should have at least 26 teeth.
  • •Patients are motivated and able to clean their teeth.
  • •Patients should not have caries, overhang restorations, crowns, bridges or implants.
  • •Adults 18-35 years old.

Exclusion Criteria

  • •Medically compromised patients.
  • •Pregnant woman.
  • •Using mouth wash or antibiotic in last 3 months.

Arms & Interventions

Interdental brush

Experimental

Participants used an interdental brush twice daily for interdental cleaning on the assigned side

Intervention: Interdental brush (Device)

Water Flosser

Experimental

Participants used a water flosser twice daily for interdental cleaning on the other assigned side

Intervention: Water floss (Device)

Outcomes

Primary Outcomes

Plaque Index

Time Frame: Baseline, 2 weeks, 4 weeks, 2 month and 3 months

Plaque accumulation assessed using the Rustogi Modified Navy Plaque Index (RMNPI) on designated tooth surfaces in the sides assigned to interdental brush and water flosser. The tooth was divided into multiple zones as the following : Whole mouth: areas A,B,C,D,E,F,G and H. Marginal (gum line): areas A,B and C. Interproximal: areas D and F 0 score was given the area where there is no plaque. 1 score was given in the area where there is plaque The minimum plaque score per surface (buccal or lingual) is zero, and the maximum plaque score per surface is 8 Intraoral photos using professional camera were taken for all teeth and all surfaces to record the plaque score.

Plaque Index

Time Frame: Baseline, 2 weeks, 4 weeks, 2 month and 3 months

Plaque accumulation assessed using the Rustogi Modified Navy Plaque Index (RMNPI) on designated tooth surfaces in the sides assigned to interdental brush and water flosser. The tooth was divided into multiple zones as the following : Whole mouth: areas A,B,C,D,E,F,G and H. Marginal (gum line): areas A,B and C. Interproximal: areas D and F 0 score was given the area where there is no plaque. 1 score was given in the area where there is plaque The minimum plaque score per surface (buccal or lingual) is zero, and the maximum plaque score per surface is 8 Intraoral photos using professional camera were taken for all teeth and all surfaces to record the plaque score.

Secondary Outcomes

  • Visual Analog Scale (VAS)(2 Weeks, 4 weeks, 2months, and 3months)
  • Visual Analog Scale (VAS)(2 Weeks, 4 weeks, 2months, and 3months)
  • Gingival Index(Baseline, 2 weeks, 4 weeks, 2 months ,and 3 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Lana Bader

Dr, Assistant Professor

Jordan University of Science and Technology

Study Sites (1)

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