Effects of an Oxalate Containing Product on Dentinal Hypersensitivity With Dental Prophylaxis
NCT ID: NCT02481557
Last Updated: 2019-06-11
Study Results
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View full resultsBasic Information
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COMPLETED
NA
36 participants
INTERVENTIONAL
2015-06-30
2015-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Oxalate Salt Solution
Professionally applied
Oxalate Salt Solution
Applied by dentist
No Treatment
No Treatment
No interventions assigned to this group
Interventions
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Oxalate Salt Solution
Applied by dentist
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, 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 at least one tooth with a Schiff sensitivity score of at least 1 in response to air challenge and a Yeaple Probe score of 10-40 in response to tactile 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 orthodontic appliances
18 Years
ALL
Yes
Sponsors
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Procter and Gamble
INDUSTRY
Responsible Party
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Locations
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Silverstone Research Group
Las Vegas, Nevada, United States
Countries
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Other Identifiers
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2015069
Identifier Type: -
Identifier Source: org_study_id
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