Evaluate Inflammation Caused by Gingivitis in Adults

The purpose of this study is to compare the anti-inflammatory efficacy of a dentifrice

Study Overview

• Status: Completed
• Conditions: Gingivitis
• Intervention / Treatment: Drug: Triclosan/Copolymer/fluoride toothpaste; Drug: sodium monofluorophosphate toothpaste

• Study Type: Interventional
• Enrollment (Actual): 49
• Phase: Phase 4

Contacts and Locations

Study Locations

• United States
  • North Carolina
    • Chapel Hill, North Carolina, United States, 27599
      • University of North Carolina

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 60 years (Adult)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Subjects must be adult males or females 18 to 60 years old
• Subjects must be able and willing to follow study procedures and instructions
• Subjects must have generalized, moderate plaque-associated gingivitis as determined by the Investigator or designee during the screening examination
• Subjects must present with at least 20 teeth in the functional dentition, excluding third molars
• Each subject must have at least four teeth with probing depths of 4-5 millimeters and at least 30% of sites bleeding to gentle probing

Exclusion Criteria:

• Subjects who have chronically used (two weeks or more) Total (Triclosan/Copolymer) dentifrice within 6 months prior to enrollment
• Subjects with gross oral pathology, including widespread caries or chronic neglect, extensive restoration, pre-existing gross plaque and calculus, or soft or hard tissue tumor of the oral cavity
• Subjects with periodontitis as indicated by periodontal pocketing 6 millimeters at screening
• Subjects with a history of early onset periodontitis or acute necrotizing ulcerative gingivitis
• Subjects with concomitant endodontic or periodontal therapy other than prophylaxis within 6 months prior to enrollment
• Subjects with orthodontic appliances or removable partial dentures
• Subjects chronically treated (two weeks or more) with any medication known to affect inflammation or periodontal status or (aspirin, nonsteroidal anti-inflammatory drugs, steroids, statins, phenytoin, calcium antagonists, cyclosporin and coumadin) within one month of the screening examination. All other medications for chronic medical conditions should be initiated at least three months prior to enrollment
• Subjects who currently smoke or who report using tobacco products within one year of screening.
• Subjects who have been treated with antibiotics for medical or dental reasons within 3 months prior to enrollment
• Subjects having clinically significant or unstable organic disease; subjects having compromised healing potential such as those with diabetes mellitus or connective tissue disorders; subjects having heart murmurs, histories of rheumatic fever, valvular disease or prosthetic joint replacement necessitating antibiotic prophylaxis
• Female subjects who report being pregnant
• Subjects who use hormonal contraceptives must have started the method 30 days prior to the screening examination.
• Subjects with active infectious diseases such as hepatitis, human immunodeficiency virus or Tuberculosis
• Subjects diagnosed with human immunodeficiency virus (HIV) or subjects that are immunocompromised as determined by the Investigator
• Medical condition which precludes not eating/drinking for approximately 8 hours.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Double

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: Total Toothpaste; Triclosan/Copolymer/fluoride toothpaste	Drug: Triclosan/Copolymer/fluoride toothpaste; Twice daily usage; Other Names: Total toothpaste
Placebo Comparator: Fluoride toothpaste; sodium monofluorophosphate toothpaste	Drug: sodium monofluorophosphate toothpaste; Twice daily usage; Other Names: Colgate cavity protection toothpaste

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Level of Gingival Crevicular Fluid Interleukin - 1 (GCF IL-1) at 2 Hours	Levels of Gingival crevicular fluid Interleukin - 1 (GCF IL-1)(weight in micrograms)	4 weeks
Level of Gingival Crevicular Fluid Interleukin - 6(GCF IL-6) at 2 Hours	Levels of Gingival crevicular fluid Interleukin - 6 (GCF IL-6) (weight in micrograms)	4 weeks

Collaborators and Investigators

• Sponsor: Colgate Palmolive
• Investigators: Principal Investigator: David Paquette, DMD

Study record dates

Study Major Dates

• Study Start: January 1, 2007
• Primary Completion (Actual): August 1, 2008
• Study Completion (Actual): August 1, 2008

Study Registration Dates

• First Submitted: September 26, 2008
• First Submitted That Met QC Criteria: June 3, 2009
• First Posted (Estimate): July 17, 2009

Study Record Updates

• Last Update Posted (Estimate): August 27, 2015
• Last Update Submitted That Met QC Criteria: August 18, 2015
• Last Verified: August 1, 2015

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Pathologic Processes; Infections; Stomatognathic Diseases; Periodontal Diseases; Mouth Diseases; Gingival Diseases; Inflammation; Gingivitis; Physiological Effects of Drugs; Molecular Mechanisms of Pharmacological Action; Anti-Infective Agents, Local; Anti-Infective Agents; Antimetabolites; Protective Agents; Hypolipidemic Agents; Lipid Regulating Agents; Cariostatic Agents; Fatty Acid Synthesis Inhibitors; Fluorides; Fluorophosphate; Triclosan
• Other Study ID Numbers: CRO-1005-INF-UNC-FP