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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05906797
Other study ID # 121-22
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 7, 2020
Est. completion date December 12, 2023

Study information

Verified date December 2023
Source University of Catania
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A double-blind randomized-controlled clinical trial is conducted in order to evaluate the impact of non-surgical periodontal treatment on endothelial dysfunction parameters in subjects with periodontitis and without any cardiovascular disease.


Description:

A double-blind randomized-controlled clinical trial is conducted in order to evaluate the impact of non-surgical periodontal treatment on endothelial dysfunction parameters in subjects with periodontitis and without any cardiovascular disease. 60 patients: 30 with periodontitis and 30 with healthy controls and without periodontitis history. All the patients are assessed for clinical, periodontal, blood and non-invasive ultrasound cardiovascular parameters. Measurements are taken before and after initial periodontal treatment in the periodontal subjects.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date December 12, 2023
Est. primary completion date October 30, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility PERIODONTITIS GROUP Inclusion Criteria: - Clinically diagnosed with periodontitis according to the EFP/AAP 2017 criteria. Exclusion Criteria: - Periodontal treatment, antibiotics, NSAIDs, immunosuppressants during the last 6 months. - Pregnancy. - Cardiovascular Diseases. HEALTHY GROUP Inclusion Criteria: - Clinically diagnosed with healthy periodontum withouth periodontitis history according to the EFP/AAP 2017 criteria. Exclusion Criteria: - Scaling, antibiotics, NSAIDs, immunosuppressants during the last 6 months. - Pregnancy. - Cardiovascular Diseases.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Non-surgical periodontal treatment
Subgingival biofilm ultrasonic debridement

Locations

Country Name City State
Italy AOU Policlinico G. Rodolico Catania

Sponsors (1)

Lead Sponsor Collaborator
University of Catania

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pulse Wave Velocity carotid-femoral (PWV-CF) The speed of pulse wave propagation between carotid-femoral sites 8 weeks
Primary Pulse Wave Velocity carotid-femoral (PWV-CR) The speed of pulse wave propagation between carotid-radial sites 8 weeks
Primary Carotid Intima-Media Thickness (CIMT) The thickness of the carotid intima and media 8 weeks
Primary Distensibility Coefficient (DC) The relative change in luminal area during systole for a given pressure change (pulsed pressure), will be calculated assuming the lumen to be circular. 8 weeks
Primary Advanced Glycation End products (AGEs) A group of endogenous heterogeneous compounds that are constantly formed under physiological conditions with prooxidant and cytotoxic properties. Measurements are performed by fluorescence spectroscopy technique. 8 weeks
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