Effect of Intensive Periodontal Therapy on Vascular Function

NCT00327561 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2006-05-18

No results posted yet for this study

Summary

The hypothesis of the existence of a causal association between the systemic infectious/inflammatory burden represented by periodontitis and endothelial function assessed by flow mediated dilatation of the brachial artery (FMD) is the subject of the proposed investigation.

The objective of this randomized controlled clinical trial is to evaluate the effects of periodontal therapy on endothelial function assessed by Flow mediated dilatation (FMD).

The rationale for this project is twofold:

* Establish the extent of acute systemic inflammation and endothelial dysfunction associated with the delivery of subgingival instrumentation for the treatment of chronic periodontitis
* Establish whether or not improved control of chronic periodontal infections results in improved endothelial function and thus the existence of a causal association between periodontitis and endothelial dysfunction.

Conditions

  • Periodontitis

Interventions

PROCEDURE

Intensive periodontal therapy

PROCEDURE

Community based periodontal therapy

Sponsors & Collaborators

  • University College London Hospitals

    collaborator OTHER
  • British Heart Foundation

    collaborator OTHER
  • The European Research Group on Periodontology (ERGOPerio)

    collaborator NETWORK
  • Johnson & Johnson

    collaborator INDUSTRY
  • CORDA, The Heart Charity

    collaborator OTHER
  • European Social Fund

    collaborator OTHER
  • Italian Society of Periodontology

    collaborator UNKNOWN
  • Eastman Dental Insitute and Hospital

    lead OTHER

Principal Investigators

  • Maurizio Tonetti, DMD PhD · University College London Hospitals and University of Connecticut Health Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
35 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-09-30
Completion
2005-03-31

Countries

  • United Kingdom

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00327561 on ClinicalTrials.gov