Suspended

Periodontal Disease and Cardiovascular Disease

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being tested

Triclosan

+ Fluoride

Drug
Who is being recruted

Stomatognathic Diseases

+ Mouth Diseases

+ Periodontal Diseases

From 18 to 75 Years
+8 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Treatment Study

Placebo-ControlledPhase 3
Interventional
Study Start: November 2000
See protocol details

Summary

Principal SponsorColgate Palmolive
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: November 1, 2000

Actual date on which the first participant was enrolled.

To access the influence of triclosan dentifrice on the progression of periodontal disease in patients with coronary heart disease.

Official TitlePeriodontal Disease and Cardiovascular Disease
NCT00763165
Principal SponsorColgate Palmolive
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

438 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 75 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Stomatognathic DiseasesMouth DiseasesPeriodontal Diseases

Criteria

3 inclusion criteria required to participate
A minimum of 12 uncrowned teeth other than 3rd molars

Age 18 to 75 years

Informed consent

5 exclusion criteria prevent from participating
Prosthetic heart valves

Prosthetic joint replacement

Previous infective endocarditis

Requirement for antibiotic cover for dental treatment

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

50% chance of being blinded to the placebo group

Treatment Groups

Group I

Active Comparator

Group II

Placebo

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Discipline of Medicine

Chermside, AustraliaOpen Discipline of Medicine in Google Maps
SuspendedOne Study Center