Effects of an Oxalate Containing Product on Dentinal Hypersensitivity With Dental Prophylaxis

NCT ID: NCT02481557

Last Updated: 2019-06-11

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

36 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-06-30

Study Completion Date

2015-06-30

Brief Summary

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This study will assess sensitivity during a dental prophylaxis with or without the use of a potassium oxalate salt solution.

Detailed Description

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Conditions

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Dentin Sensitivity

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Oxalate Salt Solution

Professionally applied

Group Type EXPERIMENTAL

Oxalate Salt Solution

Intervention Type DEVICE

Applied by dentist

No Treatment

No Treatment

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Oxalate Salt Solution

Applied by dentist

Intervention Type DEVICE

Eligibility Criteria

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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
* 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

* 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 orthodontic appliances
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Procter and Gamble

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Silverstone Research Group

Las Vegas, Nevada, United States

Site Status

Countries

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United States

Other Identifiers

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2015069

Identifier Type: -

Identifier Source: org_study_id

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