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A Two-Week Study of Clinical Safety and Saliva Flow Quantification

NCT05645705 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 270

Last updated 2023-10-10

No results posted yet for this study

Summary

The purpose of this study is to assess the oral tissue tolerance (tissues within the mouth) for irritation caused by added ingredients in mouthwashes. This will be assessed based on oral tissue exams and adverse reactions.

Conditions

  • Healthy

Interventions

OTHER

Colgate Cavity Protection Toothpaste

Participants will use Colgate Cavity Protection Toothpaste for brushing teeth twice daily.

OTHER

LISTERINE Cool Mint Antiseptic Mouthwash

Participants will use 20 mL of LISTERINE Cool Mint Antiseptic Mouthwash for 30 seconds after brushing twice daily.

OTHER

Listerine Advanced Gum Alcohol

Participants will use 20 mL of Listerine Advanced Gum Alcohol Rinse for 30 seconds after brushing twice daily.

OTHER

Listerine Advanced Gum Zero

Participants will use 20 mL of Listerine Advanced Gum Zero Rinse for 30 seconds after brushing twice daily.

OTHER

LISTERINE ULTRACLEAN Tartar Control Antiseptic Mouthwash Cool Mint

Participants will use 20 mL of LISTERINE ULTRACLEAN Tartar Control Antiseptic Mouthwash Cool Mint Rinse for 30 seconds after brushing twice daily.

Sponsors & Collaborators

  • Johnson & Johnson Consumer Inc. (J&JCI)

    lead INDUSTRY

Principal Investigators

  • Jeffery Milleman, DDS · Salus Research, Inc.

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-11-28
Primary Completion
2022-12-16
Completion
2022-12-16

Countries

  • United States

Study Locations

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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 NCT05645705 on ClinicalTrials.gov