NUPRO Sensodyne Prophylaxis Paste With NovaMin Sensitivity Relief Study

Status Completed

Clinical Trial Summary

The study is intended to verify through clinical measurement that the NUPRO Sensodyne Prophylaxis Paste with Novamin provides immediate sensitivity relief as well as extended relief up to 28 days.

Clinical Trial Description

It is hypothesized that the prophy paste with Novamin will give patients immediate sensitivity relief, as well as sensitivity relief up to 4 weeks (28 days) after measurement. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01669785
Study type	Interventional
Source	Dentsply International
Contact
Status	Completed
Phase	N/A
Start date	March 2012
Completion date	May 2012

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See also
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