Overview

Evaluate Clinical Research From Commerical Oral Care Products

Status:
Completed
Trial end date:
2008-04-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to conduct a clinical study comparing anti-plaque efficacy of commercial oral care products.
Phase:
Phase 3
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Colgate Palmolive
Treatments:
Chlorhexidine
Chlorhexidine gluconate
Fluorides
Fluorophosphate
Sodium Fluoride
Triclosan
Criteria
Inclusion Criteria:

- Male or female volunteers 18-65 years of age

- Good general health

- Must sign informed consent form

- Minimum of 20 natural uncrowned teeth (excluding third molars) must be present.

- 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:

- Subjects unable or unwilling to sign the informed consent form.

- Medical condition which requires pre-medication prior to dental visits/procedures

- Moderate or advanced periodontal disease or heavy dental tartar (calculus) requiring
more than one visit of cleaning sessions

- 2 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.

- 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 1 week prior to enrollment into this
study.

- Allergy to chlorhexidine

- Use of tobacco products

- Subjects who must receive dental treatment during the study dates.

- Current use of Antibiotics for any purpose.

- Presence of an orthodontic appliance.

- History of allergy to common dentifrice ingredients.

- Immune compromised individuals (HIV, AIDS, immuno suppressive drug therapy)