- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02243046
The Clinical Investigation of a Zinc Based Toothpaste in Reducing Plaque and Gingivitis
February 21, 2019 updated by: Colgate Palmolive
The Clinical Investigation of a Zinc Based Toothpaste as Compared to a Triclosan Based Toothpaste and Colgate Fluoride Toothpaste in Reducing Established Plaque and Gingivitis - a Six-month Study.
This is a six (6) month, double-blind, parallel, controlled clinical trial utilizing one hundred and sixty (160) adults to evaluate the reduction of dental plaque and gingivitis.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
162
Phase
- Phase 2
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Santo Domingo, Dominican Republic
- Spa Dental
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 70 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria
- Subjects, ages 18-70, inclusive.
- Availability for the six-month duration of the clinical research study.
- Good General health.
- Minimum of 20 uncrowned permanent natural teeth (excluding third molars).
- Initial gingivitis index of at least 1.0 as determined by the use of the Loe and Silness Gingival Index.
- Initial plaque index of at least 1.5 as determined by the use of the Quigley and Hein Plaque Index (Turesky Modification).
- Signed Informed Consent Form.
Exclusion Criteria
- Presence of orthodontic bands.
- Presence of partial removable dentures.
- Tumor(s) of the soft or hard tissues of the oral cavity.
- Advanced periodontal disease (purulent exudate, tooth mobility, and/or extensive loss of periodontal attachment or alveolar bone).
- Five or more carious lesions requiring immediate restorative treatment.
- Antibiotic use any time during the one-month period prior to entry into the study.
- Participation in any other clinical study or test panel within the one month prior to entry into the study.
- Dental prophylaxis during the past two weeks prior to baseline examinations.
- History of allergies to oral care/personal care consumer products or their ingredients.
- On any prescription medicines that might interfere with the study outcome.
- An existing medical condition that prohibits eating or drinking for periods up to 4 hours.
- History of alcohol or drug abuse.
- Pregnant or lactating subjects.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: DOUBLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
PLACEBO_COMPARATOR: Control toothpaste
1450 ppm Fluoride toothpaste
|
1450 ppm fluoride toothpaste control - Subjects will brush their whole mouth with the control toothpaste 2 times/day for 1 minute each time and rinse with water after brushing.
This daily brushing routine will continue for the six (6) month study.
Other Names:
|
|
EXPERIMENTAL: Experimental toothpaste
1450 ppm sodium fluoride toothpaste with a zinc base
|
1450 ppm sodium fluoride/zinc base toothpaste - Subjects will brush their whole mouth with a fluoride/zinc toothpaste 2 times/day for 1 minute each time and rinse with water after brushing.
This daily brushing routine will continue for the six (6) month study.
|
|
ACTIVE_COMPARATOR: Active comparator
1450 ppm sodium fluoride/triclosan toothpaste
|
1450 ppm sodium fluoride/triclosan toothpaste - Subjects will brush their whole mouth with this toothpaste 2 times/day for 1 minute each time and rinse with water after brushing.
This daily brushing routine will continue for the six (6) month study.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dental Plaque Scores
Time Frame: Baseline
|
Dental Plaque (Quigley-Hein, Turesky Modification Index) Units on a scale 0 to 5 (0 = no plaque, 1 = separate flecks of plaque on the tooth, 2 = a thin continuous band of plaque, 3 = a band of plaque up to one-third of the tooth, 4 = plaque covering up to two thirds of the of the tooth, 5 = plaque covering two-thirds or more of the crown of the tooth)
|
Baseline
|
|
Gingivitis Scores
Time Frame: Baseline
|
Gingivitis scale (Loe & Silness Gingival Index) Units on a scale 0 to 3 (0 = no inflammation, 1 = Mild inflammation-slight change in color and little change in texture 2 = Moderate inflammation-moderate glazing, redness, edema and hypertrophy.
Tendency to bleed upon probing.
3 = Severe inflammation-marked redness and hypertrophy.
Tendency to spontaneous bleeding)
|
Baseline
|
|
Gingivitis Scores
Time Frame: 3 months (from Baseline)
|
Gingivitis scale (Loe & Silness Gingival Index) Units on a scale 0 to 3 (0 = no inflammation, 1 = Mild inflammation-slight change in color and little change in texture 2 = Moderate inflammation-moderate glazing, redness, edema and hypertrophy.
Tendency to bleed upon probing.
3 = Severe inflammation-marked redness and hypertrophy.
Tendency to spontaneous bleeding)
|
3 months (from Baseline)
|
|
Gingivitis Scores
Time Frame: 6 months (from Baseline)
|
Gingivitis scale (Loe & Silness Gingival Index) Units on a scale 0 to 3 (0 = no inflammation, 1 = Mild inflammation-slight change in color and little change in texture 2 = Moderate inflammation-moderate glazing, redness, edema and hypertrophy.
Tendency to bleed upon probing.
3 = Severe inflammation-marked redness and hypertrophy.
Tendency to spontaneous bleeding)
|
6 months (from Baseline)
|
|
Dental Plaque Scores
Time Frame: 3 months (from Baseline)
|
Dental Plaque (Quigley-Hein, Turesky Modification Index) Units on a scale 0 to 5 (0 = no plaque, 1 = separate flecks of plaque on the tooth, 2 = a thin continuous band of plaque, 3 = a band of plaque up to one-third of the tooth, 4 = plaque covering up to two thirds of the of the tooth, 5 = plaque covering two-thirds or more of the crown of the tooth)
|
3 months (from Baseline)
|
|
Dental Plaque Scores
Time Frame: 6 months (from Baseline)
|
Dental Plaque (Quigley-Hein, Turesky Modification Index) Units on a scale 0 to 5 (0 = no plaque, 1 = separate flecks of plaque on the tooth, 2 = a thin continuous band of plaque, 3 = a band of plaque up to one-third of the tooth, 4 = plaque covering up to two thirds of the of the tooth, 5 = plaque covering two-thirds or more of the crown of the tooth)
|
6 months (from Baseline)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
December 1, 2014
Primary Completion (ACTUAL)
May 1, 2015
Study Completion (ACTUAL)
May 1, 2015
Study Registration Dates
First Submitted
September 16, 2014
First Submitted That Met QC Criteria
September 16, 2014
First Posted (ESTIMATE)
September 17, 2014
Study Record Updates
Last Update Posted (ACTUAL)
February 25, 2019
Last Update Submitted That Met QC Criteria
February 21, 2019
Last Verified
July 1, 2015
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CRO-2014-11-PG-ZNPTCN-ED
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Dental Plaque and Gingivitis
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Colgate PalmoliveFederal University of PelotasCompletedGingivitis | Dental Plaque | Dental Plaque Induced Gingivitis | Dental Plaque and GingivitisBrazil
-
Ankara UniversityThe Scientific and Technological Research Council of TurkeyCompletedPlaque-Induced GingivitisTurkey (Türkiye)
-
Koite Health OyUniversity of Helsinki; Tampere UniversityCompletedPeriodontitis | Plaque Induced Gingivitis | Plaque, DentalFinland
-
University of OsloCompleted
-
Kumeran A/L MohanInternational Islamic University MalaysiaRecruitingDental Plaque and Gingivitis | Oral Hygiene Reinforcement During Fixed Orthodontic TreatmentMalaysia
-
Dimitrie Cantemir UniversityCompletedOrthodontic Appliances, Adverse Effects,Gingivitis, Dental Plaque, Periodontal DiseasesRomania
-
Colgate PalmoliveCompleted
-
Colgate PalmoliveNot yet recruitingGingivitis | Plaque, DentalChina
-
Colgate PalmoliveActive, not recruitingGingivitis | Plaque, DentalUnited States
-
University of California, Los AngelesCompletedDental Plaque | Dental Plaque Induced GingivitisUnited States
Clinical Trials on Control toothpaste
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Unilever R&DRecruitingDental Plaque | Gingival Inflammation | Gingival BleedingIndonesia
-
The Affiliated Hospital of Qingdao UniversityCompleted
-
Church & Dwight Company, Inc.CompletedDental CariesUnited States
-
Church & Dwight Company, Inc.CompletedDental CariesUnited States
-
GlaxoSmithKlineCompletedHypersensitivity | Dentinal SensitivityUnited States
-
Colgate PalmoliveCompletedDentin HypersensitivityChina
-
Ministry of Health, Saudi ArabiaUnknown
-
University of ZagrebUnknown
-
Colgate PalmoliveWithdrawn
-
Unilever R&DIntertekCompleted