A Pilot Study to Assess Dry Mouth Relief After Using an Experimental Mouth Rinse

NCT04152642 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 22

Last updated 2021-02-02

Study results available
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Summary

The objective of this pilot study is to determine if an experimental mouth rinse and a marketed dry mouth rinse are more effective in relieving dry mouth compared to water.

Conditions

Interventions

DEVICE

Marketed Dry Mouth Rinse

relieves dry mouth symptoms by physically coating oral mucosal surfaces.

OTHER

Water control

negative control

DEVICE

Experimental Dry Mouth Rinse

relieves dry mouth symptoms by physically coating oral mucosal surfaces.

Sponsors & Collaborators

  • Procter and Gamble

    lead INDUSTRY

Principal Investigators

  • Malgorzata Klukowska, DDS · Procter and Gamble

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-11-04
Primary Completion
2019-12-05
Completion
2019-12-05
FDA Device
Yes

Countries

  • United States

Study Locations

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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 NCT04152642 on ClinicalTrials.gov