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3M Oral Rinse Incidence and Patient Acceptance of Sloughing When Used With Sodium Lauryl Sulfate (SLS) Toothpastes

NCT04601103 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 53

Last updated 2024-10-01

Study results available
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Summary

The primary objective of this study is to evaluate the incidence of oral tissue sloughing through self-report by study subjects and by professional dental examinations.

Conditions

  • Oral Mucosal Disorder

Interventions

DRUG

No SLS toothpaste

Toothpaste no Sodium Lauryl Sulfate

DRUG

Medium SLS toothpaste

Less than or equal to X ppm Sodium Lauryl Sulfate

DRUG

High SLS toothpaste

More than or equal to X ppm Sodium Lauryl Sulfate

DEVICE

Anti-plaque

Rinse prevents bacterial adherence to teeth

Sponsors & Collaborators

  • 3M

    collaborator INDUSTRY

  • Solventum US LLC

    lead INDUSTRY

Principal Investigators

  • Brenda C Coalwell, BA · 3M Health Care Business Group

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
SINGLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2020-01-06
Primary Completion
2020-03-10
Completion
2020-03-10
FDA Device
Yes

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 NCT04601103 on ClinicalTrials.gov