The Efficacy of a Dentifrice in Providing Relief From the Pain of Dentinal Hypersensitivity
NCT ID: NCT01592864
Last Updated: 2014-03-10
Study Results
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View full resultsBasic Information
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COMPLETED
PHASE3
120 participants
INTERVENTIONAL
2012-03-31
2012-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Arm 1
Dentifrice containing stannous fluoride
Stannous Fluoride
dentifice
Arm 2
Marketed dentifrice containing Sodium Monofluorophosphate
Sodium Monofluorophosphate
dentifrice
Interventions
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Stannous Fluoride
dentifice
Sodium Monofluorophosphate
dentifrice
Eligibility Criteria
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Inclusion Criteria
\- none
18 Years
65 Years
ALL
Yes
Sponsors
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GlaxoSmithKline
INDUSTRY
Responsible Party
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Principal Investigators
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GSK Clinical Trials
Role: STUDY_DIRECTOR
GlaxoSmithKline
Locations
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BioSci Research America, Inc.
Las Vegas, Nevada, United States
Countries
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Other Identifiers
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RH01325
Identifier Type: -
Identifier Source: org_study_id
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