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Trial record 20 of 43 for:    FLUORIDE ION AND TRICLOSAN

Development of Clinical Method to Determination Triclosan Retention in Plaque Following Brushing.

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00966953
Recruitment Status : Completed
First Posted : August 27, 2009
Results First Posted : August 27, 2009
Last Update Posted : September 22, 2009
Information provided by:
Colgate Palmolive

Brief Summary:
Clinical research study to determine the anti-plaque efficacy of prototype dentifrices via a 4-day brushing regiment

Condition or disease Intervention/treatment Phase
Gingival Diseases Drug: Fluoride Drug: Triclosan/Fluoride toothpaste Other: antibacterial plant extract Phase 3

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 25 participants
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Double (Participant, Investigator)
Primary Purpose: Treatment
Official Title: Development of Clinical Method to Determination Triclosan Retention in Plaque Following Brushing.
Study Start Date : October 2007
Actual Primary Completion Date : January 2008
Actual Study Completion Date : January 2008

Resource links provided by the National Library of Medicine

Drug Information available for: Triclosan

Arm Intervention/treatment
Placebo Comparator: Fluoride Toothpaste
fluoride control
Drug: Fluoride
Brush twice daily

Active Comparator: Total/Whitening
positive control
Drug: Triclosan/Fluoride toothpaste
Brush twice daily

Experimental: antibacterial plant extract 1
Drug: Fluoride
Brush twice daily
Other Name: honokiol

Experimental: antibacterial plant extract 2
Drug: Fluoride
Brush twice daily

Other: antibacterial plant extract
Brush twice daily
Other Name: Honokiol

Primary Outcome Measures :
  1. Plaque Index [ Time Frame: 8 weeks ]

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 65 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • Male or female volunteers 18-65 years of age.
  • Good general health.
  • Must sign informed consent form.
  • Must discontinue oral hygiene on the mornings of each appointment and between sampling periods.
  • No history of allergy to personal care consumer products, or their ingredients, relevant to any ingredient in the test products as determined by the dental/medical professional monitoring the study.

Exclusion Criteria:

  • Medical condition which requires pre-medication prior to dental procedures/visits.
  • Medical condition which precludes eating/drinking for 12 hrs.
  • History of allergy to common dentifrice ingredients.
  • Subjects unable or unwilling to sign the informed consent form.
  • Moderate or advanced periodontal disease.
  • Two or more decayed untreated dental sites at screening.
  • Other disease of the hard or soft oral tissues.
  • Impaired salivary function (e.g. Sjogren's syndrome or head and neck irradiation).
  • Use of medications that can currently affect salivary flow.
  • Current use of antibiotics.
  • Use of antibiotics or antimicrobial drugs within 30 days prior to study visit #1.
  • Pregnant or nursing women.
  • Participation in any other clinical study within 30 days prior to enrollment into this study.
  • Use of tobacco products.
  • Subjects who must receive dental treatment during the study dates.
  • Current use of Antibiotics for any purpose.
  • Immune compromised individuals (HIV,AIDS, immuno suppressive drug therapy).

Information from the National Library of Medicine

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 identifier (NCT number): NCT00966953

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United States, New York
Eastman Dental Center - University of Rochester
Rochester, New York, United States, 14642-8315
Sponsors and Collaborators
Colgate Palmolive
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Principal Investigator: Yanfang Ren, DDS

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Responsible Party: William DeVizio/VP - Clinical Research, Colgate Palmolive Identifier: NCT00966953     History of Changes
Other Study ID Numbers: ERO-0907-PLA-16-RR
First Posted: August 27, 2009    Key Record Dates
Results First Posted: August 27, 2009
Last Update Posted: September 22, 2009
Last Verified: September 2009
Additional relevant MeSH terms:
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Gingival Diseases
Periodontal Diseases
Mouth Diseases
Stomatognathic Diseases
Anti-Bacterial Agents
Cariostatic Agents
Protective Agents
Physiological Effects of Drugs
Anti-Infective Agents
Anti-Infective Agents, Local
Fatty Acid Synthesis Inhibitors
Hypolipidemic Agents
Molecular Mechanisms of Pharmacological Action
Lipid Regulating Agents
Anti-Arrhythmia Agents
Antineoplastic Agents, Phytogenic
Antineoplastic Agents
Central Nervous System Depressants
Enzyme Inhibitors
Gastrointestinal Agents
Anti-Anxiety Agents
Tranquilizing Agents
Psychotropic Drugs
Anti-Allergic Agents