A Pilot Clinical Study to Evaluate the Safety and Efficacy of Marketed Oxalate Strips Compared to a Marketed Safety Pen
NCT ID: NCT02384044
Last Updated: 2019-06-25
Study Results
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View full resultsBasic Information
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COMPLETED
NA
30 participants
INTERVENTIONAL
2015-02-28
2015-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Crest® Sensi-Stop™ Strips
Professionally Applied
Crest® Sensi-Stop™ Strips
Colgate® Sensitivity Relief Pen
Professionally Applied
Colgate® Sensitivity Relief Pen
Interventions
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Crest® Sensi-Stop™ Strips
Colgate® Sensitivity Relief Pen
Eligibility Criteria
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Inclusion Criteria
* sign an informed consent form and be given a copy
* be in good general health as determined by the Investigator/designee
* agree to delay any elective dentistry, including dental prophylaxis, and to report any dentistry received during the course of the study
* agree to not participate in any other oral care study for the duration of this study
* agree to return for scheduled visits and follow all study procedures
* have dentinal hypersensitivity with at least one tooth with a Schiff sensitivity score of at least 1 in response to the cold water challenge
Exclusion Criteria
* 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
* a history of kidney stones
* self-reported pregnancy or nursing
* known allergies to the following ingredients; aqua, glycerin, cellulose gum, dipotassium oxalate, carbomer, sodium hydroxide, sodium benzoate, and potassium sorbate
18 Years
ALL
Yes
Sponsors
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Procter and Gamble
INDUSTRY
Responsible Party
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Principal Investigators
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Robert W Gerlach, DDS, MPH
Role: PRINCIPAL_INVESTIGATOR
Procter and Gamble
Locations
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Oral Health Science Center
Mason, Ohio, United States
Countries
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Other Identifiers
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2015012
Identifier Type: -
Identifier Source: org_study_id
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