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A Clinical Study to Compare Professional Treatments for Dentinal Hypersensitivity

NCT03405259 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 22

Last updated 2019-06-17

Study results available
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Summary

The objective of this study is to compare professional treatments for dentinal hypersensitivity immediately following a single, professionally-applied treatment and again approximately 2 months following treatment.

Conditions

  • Dentinal Hypersensitivity

Interventions

DEVICE

Super Seal® Desensitizer

Single dose professional application.

DEVICE

Acclean® Fluoride Varnish

Single dose professional application.

Sponsors & Collaborators

  • Procter and Gamble

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-06-26
Primary Completion
2013-09-13
Completion
2013-09-13
FDA Device
Yes

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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 NCT03405259 on ClinicalTrials.gov