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A Study to Investigate Efficacy of Two Experimental Oral Rinses in Providing Long Term Relief From Pain Derived From Exposed Dentine in Response to Chemical, Thermal, Tactile, or Osmotic Stimuli.

NCT02651467 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 221

Last updated 2018-08-27

Study results available
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Summary

This will be a single center, eight week, randomized, double blind, three treatment arm, parallel design, stratified (by mean baseline Schiff Sensitivity Score of the two selected test teeth) study in healthy participants.

Conditions

  • Dentin Sensitivity

Interventions

OTHER

Experimental Oral Rinse 1 (1.5% w/w KOX, 0ppm F, pH 7.0)

1.5% w/w KOX, 0ppm F, pH 7.0

OTHER

Experimental Oral Rinse 2 (2.0% w/w KOX, 45ppm F, pH 4.5)

2.0% w/w KOX, 45ppm F, pH 4.5

OTHER

Placebo Oral Rinse (0% w/w KOX 0ppm F, pH 4.5 )

0% w/w KOX 0ppm F, pH 4.5

Sponsors & Collaborators

Principal Investigators

  • GSK Clinical Trials · GlaxoSmithKline

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2016-01-04
Primary Completion
2016-04-01
Completion
2016-04-22

Countries

  • United States

Study Locations

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Entities

Companies

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 NCT02651467 on ClinicalTrials.gov