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A Study to Evaluate the Safety and Efficacy of an Oxalate Strip on Adjacent Teeth With Dentinal Hypersensitivity

Procter & Gamble (P&G) logo

Procter & Gamble (P&G)

Status

Completed

Conditions

Dentin Sensitivity

Treatments

Device: Crest® Sensi-Stop™ Strips

Study type

Interventional

Funder types

Industry

Identifiers

NCT02293044
2014115

Details and patient eligibility

About

This study will compare the safety and effectiveness of a potassium oxalate desensitizer on adjacent teeth with dentinal hypersensitivity.

Enrollment

15 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • be at least 18 years of age
  • sign an informed consent form and be given a copy
  • be in good general health as determined by the Investigator/designee
  • have at least one pair of adjacent teeth, each of which has a screening score of - -greater than or equal to 1 on the Schiff Sensitivity Scale in response to the cold water challenge.

Exclusion criteria

  • severe periodontal disease, as characterized by purulent exudate, generalized mobility, and/or severe recession
  • active treatment for periodontitis
  • any diseases or conditions that might interfere with the subject safely completing the study
  • inability to undergo study procedures
  • fixed facial orthodontic appliances
  • self-reported pregnancy or nursing
  • a history of kidney stones
  • known allergies to the following ingredients; aqua, glycerin, cellulose gum, dipotassium oxalate, carbomer, sodium hydroxide, sodium benzoate, and potassium sorbate.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

15 participants in 1 patient group

Crest® Sensi-Stop™ Strips
Experimental group
Description:
Self Applied
Treatment:
Device: Crest® Sensi-Stop™ Strips

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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