A Study to Investigate the Anti-Plaque Effect of AN0128 Toothpaste
Completed · Phase 1
Conditions studied: Dental Plaque
In brief
The objective of this study was to evaluate the anti-plaque efficacy of the Anacor prototype dentrifice as compared to commercial control products following a single use of the dentrifice.
Key facts
- Study ID
- NCT00762151
- Run by
- Pfizer
- People needed
- 18
- Starts
- 2007-11-01
- Expected to finish
- 2008-01-01
- Last updated by the study team
- 2019-06-05
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Must be between ages 18 to 65 years inclusive
- Have a minimum of 16 natural uncrowned teeth (excluding 3rd molars) present
- Must give written informed consent
- Be in good general health
- Must discontinue oral hygiene for 24-hours after initial appointment
- No known 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
You may not qualify if…
- Medical condition which requires pre-medication prior to dental visits/procedures
- Advanced periodontal disease
- 5 or more decayed, untreated dental sites
- Diseases of the soft or hard oral tissues
- Orthodontic appliances
- Abnormal salivary function
- Use of drugs that can affect salivary flow
- Use of antibiotics one (1) month prior to or during this study
- Use of any over the counter medications other than analgesics (i.e. aspirin, ibuprofen, acetaminophen, naproxen), unless approved by the study medical staff
- Pregnant or breastfeeding
- Participation in another clinical study in the month preceding this study
- Allergic to common dentifrice ingredients
- Immune compromised individuals (HIV, AIDS, immuno suppressive drug therapy)
- History of allergic reaction to any anti-inflammatory agents
Where it is running
- Concordia Research Laboratories — Cedar Knolls, New Jersey, United States
Full record on ClinicalTrials.gov
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