MedTrace Logo

NUPRO Sensodyne Prophylaxis Paste With NovaMin Sensitivity Relief Study

NCT01669785 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 139

Last updated 2014-08-21

Study results available
· View outcomes & findings →

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.

Conditions

  • Tooth Hypersensitivity

Interventions

DEVICE

Group C

Abrasive, flavored dental prophylaxis paste for cleaning and polishing teeth.

DEVICE

Group A

Abrasive, flavored dental prophylaxis paste for cleaning and polishing teeth.

DEVICE

Group B

Abrasive, flavored dental prophylaxis paste for cleaning and polishing teeth.

Sponsors & Collaborators

  • Dentsply International

    lead INDUSTRY

Principal Investigators

  • Jeffrey L Milleman, DDS, MPA · Salus Research

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2012-03-31
Primary Completion
2012-04-30
Completion
2012-05-31

Countries

  • United States

Study Locations

More Related Trials

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 NCT01669785 on ClinicalTrials.gov