- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03297749
Genetic Variants and Oxidative Stress as Links Between Periodontitis and Metabolic Syndrome
October 25, 2017 updated by: University College, London
The aim of this study is to investigate the systemic impact of periodontitis in patients with Metabolic Syndrome, by assessing measures of sub-clinical atherosclerosis and cardiovascular risk, microbial factors and host genetic variants, and to study the possible effect of mediators of inflammation and oxidative stress as links between the two conditions.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
This is a cross-sectional study.
102 patients with metabolic syndrome will be recruited and will have periodontal and dental examination for diagnosis of caries and periodontal diseases.
They will undergo blood, saliva, GCF and subgingival plaque sampling and a series of tests on cardiovascular disease, including measures of pulse-wave velocity,carotid intima-media thickness and echocardiography assessment.
Statistical analysis will assess associations between dental diagnoses and metabolic, cardiovascular, inflammatory, genetic, microbial and cardiovascular risk outcomes.
Study Type
Observational
Enrollment (Anticipated)
102
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Catania, Italy
- University of Catania
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-
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London, United Kingdom, EN54LU
- UCL
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 75 years (Adult, Older Adult)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Subjects with metabolic syndrome will be recruited from outpatients attending the Internal Medicine Unity at the University of Catania.
Description
Inclusion Criteria:
- Caucasian ethnicity
- Age 18- 75
- Diagnosis of metabolic syndrome
- Presence of at least 12 teeth
Exclusion Criteria:
- Pregnancy
- Presence of infectious diseases such as hepatitis and HIV
- Use of non-steroidal anti-inflammatory drugs (excluding low-dose aspirin) within one month prior to the baseline visit
- Use of systemic antibiotics within three months prior to the baseline visit
- Antibiotic pre-medication required for the performance of periodontal examination
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Cross-Sectional
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
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pulse wave velocity
Time Frame: baseline
|
baseline
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oxidative stress
Time Frame: baseline
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baseline
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carotid intima-media thickness
Time Frame: baseline
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baseline
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genetic variants
Time Frame: baseline
|
baseline
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left ventricular mass
Time Frame: baseline
|
baseline
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
inflammatory markers
Time Frame: baseline
|
baseline
|
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subgingival microbes
Time Frame: baseline
|
baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 1, 2015
Primary Completion (Actual)
September 30, 2017
Study Completion (Anticipated)
December 31, 2020
Study Registration Dates
First Submitted
September 26, 2017
First Submitted That Met QC Criteria
September 26, 2017
First Posted (Actual)
September 29, 2017
Study Record Updates
Last Update Posted (Actual)
October 26, 2017
Last Update Submitted That Met QC Criteria
October 25, 2017
Last Verified
September 1, 2017
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 4242/01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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