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NCT02476032

An Evaluation of the Efficacy of Oral-B New Product Sensi-Stop on Dentinal Hypersensitivity

University of Minnesota·ClinicalTrials.gov·device·Device trialCompleted
View on ClinicalTrials.gov →
Study focus
Disease/Condition
Tooth Sensitivity
Drug/Device/Intervention
Prof applied oxalate
Study type
Interventional
Intervention type
device
Sponsor & location
Primary sponsor
University of Minnesota
Location
Minneapolis, United States of America
Timeline & enrollment
Phase
N/A
Start date
Jul 01, 2015
End date
May 01, 2016
Enrollment
60 participants
Primary outcome

Schiff Air Test: Mean Reduction in Sensitivity Between Groups

Summary

The purpose of the study is to evaluate the efficacy of Sensi-StopTM strips (Procter &
 Gamble™) on the relief of dentinal hypersensitivity. In other words, do Sensi-StopTM strips
 (Procter & Gamble™) reduce or eliminate cold sensitivity in teeth? In addition, the
 investigators will evaluate whether there is a difference in the Sensi-StopTM strip (Procter
 & Gamble™) effectiveness when the product is placed by a dental professional compared to
 self-placement by the person with sensitive teeth. This product is not experimental.

ICD-10 classifications
Anomalies of tooth positionTeething syndromeDisturbances in tooth eruptionDisturbances in tooth formationOther disorders of tooth development
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT02476032
Type
Device Trial
About this record

Access comprehensive clinical trial information for NCT02476032 through Pure Global AI's free database. This phase not specified trial is sponsored by University of Minnesota and is currently Completed. The study focuses on Tooth Sensitivity. Target enrollment is 60 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.