The Clinical Efficacy of Three Oral Hygiene Regimens Using a Manual Toothbrush, Toothpaste and a Mouthwash in Controlling Dental Plaque and Gingivitis
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| ClinicalTrials.gov Identifier: NCT02193165 |
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Recruitment Status :
Completed
First Posted : July 17, 2014
Results First Posted : February 6, 2015
Last Update Posted : August 17, 2015
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Dental Plaque Gingivitis | Drug: triclosan/fluoride toothpaste + cetylpyridinium chloride Mouthwash Drug: stannous fluoride toothpaste + cetylpyridinium chloride Mouthwash Drug: fluoride toothpaste + fluoride Mouthwash | Phase 3 |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 120 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Triple (Participant, Investigator, Outcomes Assessor) |
| Primary Purpose: | Treatment |
| Official Title: | The Comparative Efficacy of Three Oral Hygiene Multi-component Regimens Encompassing the Use of a Manual Toothbrush, Toothpaste and a Mouthwash in Controlling Established Dental Plaque and Gingivitis. |
| Study Start Date : | July 2014 |
| Actual Primary Completion Date : | August 2014 |
| Actual Study Completion Date : | August 2014 |
| Arm | Intervention/treatment |
|---|---|
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Active Comparator: Regimen 1
triclosan/fluoride toothpaste + cetylpyridinium chloride Mouthwash
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Drug: triclosan/fluoride toothpaste + cetylpyridinium chloride Mouthwash
Brush whole mouth with Total toothpaste for 1 minute, 2 times/day for 6 weeks (study duration) using a Total 360 toothbrush. Immediately after each toothbrushing, rinse whole mouth with 20 ml of mouthwash for 30 seconds.
Other Names:
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Active Comparator: Regimen 2
stannous fluoride toothpaste + cetylpyridinium chloride Mouthwash
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Drug: stannous fluoride toothpaste + cetylpyridinium chloride Mouthwash
Brush whole mouth with Crest Pro-Health toothpaste for 1 minute, 2 times/day for 6 weeks (study duration) using an Oral B Pro-Health toothbrush. Immediately after each toothbrushing, rinse whole mouth with 20 ml of Crest Pro-Health Multi-Protection mouthwash for 30 seconds.
Other Names:
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Placebo Comparator: Regimen 3 - Control group
fluoride toothpaste + fluoride Mouthwash
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Drug: fluoride toothpaste + fluoride Mouthwash
Brush whole mouth with Crest Cavity Protection toothpaste for 1 minute, 2 times/day for 6 weeks (study duration) using an Oral B Indicator toothbrush. Immediately after each toothbrushing, rinse whole mouth with 20 ml of Crest Pro-Health For Me Breezy Mint mouthwash for 30 seconds.
Other Names:
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- 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)
- Dental Plaque Scores [ Time Frame: 4 weeks ]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)
- Dental Plaque Scores [ Time Frame: 6 weeks ]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)
- 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)
- Gingivitis Scores [ Time Frame: 4 weeks ]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)
- Gingivitis Scores [ Time Frame: 6 weeks ]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)
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| Ages Eligible for Study: | 21 Years to 70 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Male and female subjects, ages 21-70, inclusive.
- Availability for the six-week duration of the 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.
- Use of antibiotics any time during the one month 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.
- Pregnant women or women who are breast feeding.
- Dental prophylaxis received in 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 which prohibits eating or drinking for periods up to 4 hours.
- History of alcohol or drug abuse
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02193165
| Puerto Rico | |
| Centro Comercial Plaza Trujillo | |
| Trujillo Alto, Puerto Rico, 00976 | |
| Responsible Party: | Colgate Palmolive |
| ClinicalTrials.gov Identifier: | NCT02193165 |
| Other Study ID Numbers: |
CRO-2014-07-PG-REG-PR-BS |
| First Posted: | July 17, 2014 Key Record Dates |
| Results First Posted: | February 6, 2015 |
| Last Update Posted: | August 17, 2015 |
| Last Verified: | July 2015 |
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Gingivitis Dental Plaque Infections Gingival Diseases Periodontal Diseases Mouth Diseases Stomatognathic Diseases Dental Deposits Tooth Diseases Triclosan Cetylpyridinium Fluorides |
Tin Fluorides Cariostatic Agents Protective Agents Physiological Effects of Drugs Anti-Infective Agents, Local Anti-Infective Agents Fatty Acid Synthesis Inhibitors Hypolipidemic Agents Antimetabolites Molecular Mechanisms of Pharmacological Action Lipid Regulating Agents |

