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A Clinical Study to Evaluate the Efficacy of a Stannous Fluoride Dentifrice in the Relief of Dentinal Hypersensitivity in a Chinese Population

NCT04950465 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 271

Last updated 2023-10-23

Study results available
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Summary

The purpose of this study is to support long-term dentinal hypersensitivity (DH) relief claims of 0.454 percent (%) stannous fluoride (SnF2) containing toothpastes in China.

Conditions

  • Dentin Sensitivity

Interventions

OTHER

Sensodyne Sensitivity & Gum

Sensodyne Sensitivity \& Gum toothpaste containing 0.454% SnF2.

OTHER

Crest Cavity Protection Fresh Lime

Crest Cavity Protection Fresh Lime is containing 1150 parts per million fluoride as Sodium fluoride.

OTHER

Sensodyne Repair and Protect

Sensodyne Repair and Protect dentifrice containing 5.0% weight/weight calcium sodium phosphosilicate.

Sponsors & Collaborators

  • HALEON

    lead INDUSTRY

Principal Investigators

  • GSK Clinical Trials · Preventive Dentistry Depart-ment, Shanghai Ninth Peo-ple's Hospital, Shanghai Jiao-tong University, School of Medicine

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2021-07-27
Primary Completion
2022-01-25
Completion
2022-01-25

Countries

  • China

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 NCT04950465 on ClinicalTrials.gov