Completed

NUPRO(r) Sensodyne Prophylaxis Paste With NovaMin(r) for the Treatment of Dentin Hypersensitivity.

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being tested

NUPRO Classic Prophy Paste

+ NUPRO Sensodyne Prophy Paste with Novamin with fluoride.

+ NUPRO Sensodyne Prophy Paste with Novamin without fluoride.

Device
Who is being recruted

Dentin Sensitivity

+ Stomatognathic Diseases

+ Tooth Diseases

From 18 to 70 Years
+28 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Treatment Study

Interventional
Study Start: September 2011
See protocol details

Summary

Principal SponsorDentsply International
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: September 1, 2011

Actual date on which the first participant was enrolled.

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

Official TitleNUPRO(r) Sensodyne Prophylaxis Paste With NovaMin(r) for the Treatment of Dentin Hypersensitivity.
NCT01610167
Principal SponsorDentsply International
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

151 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 70 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Dentin SensitivityStomatognathic DiseasesTooth Diseases

Criteria

8 inclusion criteria required to participate
Availability to complete in the 28 day duration of the study.
Two sensitive teeth which are not adjacent to each other and preferably in different quadrants and demonstrate cervical erosion, abrasion, and gingival recession.
qualifying response to tactile stimuli as defined by a score of </= 20 grams.
Qualifying response to air blast stimuli as defined by a score of >/= 1 on the Schiff Cold Air Sensitivity Scale.
Show More Criteria
20 exclusion criteria prevent from participating
Individuals who exhibit gross oral pathology
Females who may be pregnant or lactating or intending to become pregnant
Individuals who require anesthetic during scaling
Dental pathology which may cause pain similar to tooth sensitivity
Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

3 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Active Comparator

Group II

Experimental

Group III

Experimental

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Salus Research

Fort Wayne, United StatesOpen Salus Research in Google Maps
CompletedOne Study Center