Influence of Periodontitis and Coronary Heart Disease on Galectin-3
NCT ID: NCT04564950
Last Updated: 2020-12-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
155 participants
OBSERVATIONAL
2016-04-01
2018-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
RETROSPECTIVE
Study Groups
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Control
Observation of salivary Galectin-3 levels and correlation of salivary Galectin -3 evels with periodontal disease
Observation of serum and salivary Galectin-3 levels
Observation of serum and salivary Galectin-3 levels and correlation with periodontal indices
Periodontitis
Observation of salivary Galectin-3 levels and correlation of salivary Galectin -3 evels with periodontal disease
Observation of serum and salivary Galectin-3 levels
Observation of serum and salivary Galectin-3 levels and correlation with periodontal indices
Coronary heart disease
Observation of salivary Galectin-3 levels and correlation of salivary Galectin -3 evels with periodontal disease
Observation of serum and salivary Galectin-3 levels
Observation of serum and salivary Galectin-3 levels and correlation with periodontal indices
Coronary heart disease + periodontitis
Observation of salivary Galectin-3 levels and correlation of salivary Galectin -3 evels with periodontal disease
Observation of serum and salivary Galectin-3 levels
Observation of serum and salivary Galectin-3 levels and correlation with periodontal indices
Interventions
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Observation of serum and salivary Galectin-3 levels
Observation of serum and salivary Galectin-3 levels and correlation with periodontal indices
Eligibility Criteria
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Inclusion Criteria
* CP with a minimum of 40% of sites with a clinical attachment level (CAL)
≥2mm and probing depth (PD) ≥4mm;
* Presence of at least ≥2 mm of crestal alveolar bone loss verified on digital periapical radiographs
* Presence of ≥40% sites with bleeding on probing (BOP)
Exclusion Criteria
* Intake of immunosuppressive or anti-inflammatory drugs throughout the last three months prior to the study
* Status of pregnancy or lactation
* Previous history of excessive drinking
* Allergy to local anaesthetic
* Intake of drugs that may potentially determine gingival hyperplasia such as Hydantoin, Nifedipine, Cyclosporin A or similar drugs.
30 Years
70 Years
ALL
No
Sponsors
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University of Messina
OTHER
Responsible Party
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Gaetano Isola, DDS, PhD
Principal Investigator
Locations
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University of Messina
Messina, , Italy
Countries
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Other Identifiers
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18-16-2018
Identifier Type: -
Identifier Source: org_study_id