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Periodontitis and Cardiovascular Events or "PAVE"

Not Applicable
Completed
Conditions
Cardiovascular Disease
Coronary Heart Disease
Myocardial Infarction
Cerebrovascular Accident
Interventions
Procedure: Referral
Registration Number
NCT00066053
Lead Sponsor
University at Buffalo
Brief Summary

The purpose of this study is to determine if treating periodontal infections (gum problems) will lead to fewer heart problems in patients at high risk for cardiovascular disease.

Detailed Description

There is growing evidence of a strong association between infection and atherosclerosis as well as a specific link between periodontal infection (gum problems) and heart disease. Previous studies have established possible effective treatments of periodontal disease. These treatments may lead to fewer heart events in persons at high risk for cardiovascular disease. In contrast to previous heart disease studies, the primary treatment in this project is directed toward infectious agents at periodontal sites. This project is a pilot randomized clinical trial to test the feasibility of selecting and refining a periodontal infection treatment and examining the effect of that treatment on future heart events. It is a multi-center planning and pilot study involving five investigational centers at the University at Buffalo (lead and overall coordinating center), University of North Carolina, Boston University, Kaiser Permanente/Oregon Health Science University, University of Maryland, and a data coordinating center at the University of North Carolina. Central microbiology and cytokine laboratories and a biologic specimen bank are also included. A team of cardiologists, periodontists, epidemiologists, infectious disease specialists, biostatisticians, research nurses in periodontics and cardiology, and data managers has been assembled to accomplish the research with a careful, cost-effective approach. The ultimate goal is to develop a definitive randomized clinical trial that will include about 4,000 participants from approximately 15 centers across the United States

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
303
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Community ComparatorReferralReferral to community dentist with copy of x-rays and letter with diagnosis and recomendations for treatment.
Primary Outcome Measures
NameTimeMethod
Patient outcomes are hospitalized for myocardial infarction (MI), cardiac revascularization, fatal coronary heart disease, unstable angina, and/or hospitalized ischemic stroke.One year
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University at Buffalo

🇺🇸

Buffalo, New York, United States

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