Overview

Evaluating Commercial Anti-Plaque Products and Oral Rinse

Status:
Completed
Trial end date:
2007-09-01
Target enrollment:
0
Participant gender:
All
Summary
Clinical research study to determine the anti-plaque efficacy of commerical dentifrices and an oral rinse.
Phase:
Phase 2
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Colgate Palmolive
Treatments:
Chlorhexidine
Chlorhexidine gluconate
Fluorides
Triclosan
Criteria
Inclusion Criteria:

- Male or female volunteers at least 18 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).

- 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 are currently affect salivary function.

- Use of antibiotics or antimicrobial drugs within 30 days prior to study visit #1.

- Allergy to chlorhexidine.

- Pregnant or nursing women.

- Participation in any other clinical study within 1 week 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 pre-medication for dental treatment or for any other
purpose.

- Presence of an orthodontic appliance that interferes with plaque scoring.

- History of allergy to common dentifrice ingredients.

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