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Antiplaque/Antigingivitis Efficacy of Essential Oil Mouthrinses in Six-Month Study

NCT02980497 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 370

Last updated 2016-12-02

No results posted yet for this study

Summary

The objective of this randomized, single-center, examiner-blind, controlled, parallel group, six-month clinical study is to compare the antiplaque/antigingivitis potential of a no-alcohol essential oil containing mouthrinse and an alcohol essential oil containing mouthrinse. A negative control group using only an ADA Accepted anticavity toothpaste will be included.

Conditions

  • Plaque
  • Gingivitis
  • Gum Inflammation
  • Bleeding

Interventions

OTHER

Listerine Zero Mouthwash (without alcohol)

20 ml of rinse for 30 seconds, twice a day

OTHER

Listerine Antiseptic Mouthwash (with alcohol)

20 ml of rinse for 30 seconds, twice a day

Sponsors & Collaborators

  • University of Taubate

    collaborator OTHER

  • Johnson & Johnson Consumer and Personal Products Worldwide

    lead INDUSTRY

Principal Investigators

  • Jose Cortelli, Ph. D · Universidade de Taubate

  • Sheila Cortelli, Ph.D · Universidade de Taubate

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-09-30
Primary Completion
2014-03-31
Completion
2014-03-31

Countries

  • Brazil

Study Locations

More Related Trials

Entities

Diseases

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 NCT02980497 on ClinicalTrials.gov