Study of the Anti-Inflammatory Effects of Colgate Total® During an Experimental Gingivitis Model

Completed · Not applicable

Conditions studied: Gingivitis

In brief

This study evaluates the anti-inflammatory effects of Colgate Total® during an experimental gingivitis model developed by Löe et al. Half of the participants will use Colgate Total® (which contains triclosan), while the other half will use a toothpaste which does not contain triclosan as the control.

Key facts

Study ID

NCT01799226

Run by

University of Michigan

People needed

32

Starts

2013-03-01

Expected to finish

2013-12-01

Last updated by the study team

2016-01-13

Who can join

Age: 18 and older, up to 40. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Race - all
• Gender - female or male
• Age - 18 to 40 years old
• Dentition - minimum of 20 permanent teeth
• Probing Pocket Depth of 1-4mm in all sites
• Mean Clinical Attachment Levels of 2mm on all teeth
• Bleeding Upon Probing of greater than 30% at Day -14 Study Visit
• Consent Form - read, understood, and signed
• Study Procedures - willing to follow all study procedures
• At Day 0 Study Visit, all subjects must have a BOP of less than 10%. Subjects not meeting the BOP study criteria will be asked to return in 2 weeks for a second assessment visit. Subjects who do not meet the inclusion criteria
• BOP less than 10% at the second assessment visit will be exited from the
• study

You may not qualify if…

• Medical History - a history of alcoholism or drug abuse
• Diseases of the immune system
• Medical condition that may affect outcome (neurologic or psychiatric disorders, systemic infection
• Medications - chronic medications known to affect the periodontal status (calcium antagonists anticonvulsives, immunosuppressives, anti-inflammatory medications, phenytoin, Depo-Provera contraceptive injection users
• New oral contraceptives users within 3 months of baseline or are planning on starting oral contraceptives during the study
• Hypersensitivity - previous known reaction to or oral allergy to any ingredient in the study toothpaste
• Antibiotics - antibiotic therapy within 3 months of baseline visit
• antibiotic therapy needed for infective endocarditis prophylaxis or total joint replacement
• Use of antiseptics - homecare regime using products to control dental plaque formation within 30 days prior to baseline visit
• Smoking - current smokers, smokers who quit smoking less than one year ago, or a pack-year history of more than or equal to 10 (pack-years will be calculated by multiplying the number of years smoked by the average number of cigarette packs smoked per day)
• Continine - positive urine analysis results
• Current Dental Treatment - orthodontic or periodontal treatment
• Untreated Dental Treatment - untreated carious lesions
• Defective restorations which could exacerbate during a period of oral hygiene abstinence
• Pregnant or women breast-feeding

Where it is running

• Michigan Center for Oral Health Research — Ann Arbor, Michigan, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.