Comparison of Two Interdental Cleaners

NCT ID: NCT03047759

Last Updated: 2017-02-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

70 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-07-21

Study Completion Date

2016-08-19

Brief Summary

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Comparison of Two interdental cleaning devices on plaque removal, gingivitis and bleeding.

Detailed Description

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This study measured plaque accumulation, bleeding on probing and gingivitis using the Rustogi Modification of the Navy Plaque Index, BOP and Modified Gingival Index at baseline, 2-weeks and 4-weeks.

Conditions

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Gingivitis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Investigators

Study Groups

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Intervention A

water flosser

Group Type ACTIVE_COMPARATOR

water flosser

Intervention Type DEVICE

Powered

Intervention B

air floss

Group Type ACTIVE_COMPARATOR

air floss

Intervention Type DEVICE

Powered

Interventions

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water flosser

Powered

Intervention Type DEVICE

air floss

Powered

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Healthy adult
* Non smoker
* Available for 4-weeks
* Able to provide written informed consent.
* Minimum of 20 natural teeth.
* Minimum requirement for plaque, gingivitis and bleeding.

Exclusion Criteria

* Medical condition
* No antibiotics within 6 months of study start
* Not on any medication (impact oral health).
Minimum Eligible Age

25 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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All Sum Research Center Ltd.

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Other Identifiers

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2016-WP-2

Identifier Type: -

Identifier Source: org_study_id

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