Efficacy and Safety Study of Interproximal Cleaning Modalities on Oral Health

NCT02187016 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 290

Last updated 2016-03-08

Study results available
· View outcomes & findings →

Summary

The purpose of this study is to evaluate the safety and efficacy of tooth and interproximal cleaning modalities with and without chemistry on oral health over 28 days.

Conditions

  • Gingivitis

Interventions

DEVICE

AirFloss + BreathRx

Manual Toothbrush used twice daily, 1 minute. Interproximal cleaning plus Rinse used once daily.

DEVICE

AirFloss + Listerine

Manual Toothbrush used twice daily, 1 minute. Interproximal cleaning plus Rinse used once daily.

DEVICE

Dental Floss

Manual Toothbrush used twice daily, 1 minute. Interproximal cleaning used once daily.

DEVICE

Manual Toothbrush

Manual Toothbrush used twice daily, 1 minute.

Sponsors & Collaborators

  • Philips Oral Healthcare

    lead INDUSTRY

Principal Investigators

  • Pejmon Amini, DDS · Silverston Research Group

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-06-30
Primary Completion
2014-07-31
Completion
2014-07-31

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02187016 on ClinicalTrials.gov