Endothelin Concentrations in a Population With Cardiovascular Disease and Periodonitis

NCT ID: NCT04152005

Last Updated: 2019-11-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

165 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-01-01

Study Completion Date

2018-09-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Recently, a key role played in the ethiology of periodontitis has been highlighted by a Endothelin (ET-1). ET1 possess the ability to express surface antigens of endothelial and hematopoietic stem cells and to assist in maintaining vascular integrity and the repair mechanism of the endothelium. ET originate from bone marrow

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The aim of the present study was to investigate the association between ET-1 in patients with periodontitis. Furthermore, the objective was to determine if the periodontal status influenced ET-1 levels.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Serum; Disease

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_CONTROL

Study Time Perspective

CROSS_SECTIONAL

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Control

Evaluation of ET-1 level and correlation of ET-1 levels with periodontal and cardiovascular disease

Observation

Intervention Type OTHER

Evaluation of ET-1 level and correlation of ET-1 levels with periodontal and cardiovascular disease

Periodontitis

Evaluation of ET-1 level and correlation of ET-1 levels with periodontal and cardiovascular disease

Observation

Intervention Type OTHER

Evaluation of ET-1 level and correlation of ET-1 levels with periodontal and cardiovascular disease

Cardiovascular

Evaluation of ET-1 level and correlation of ET-1 levels with periodontal and cardiovascular disease

Observation

Intervention Type OTHER

Evaluation of ET-1 level and correlation of ET-1 levels with periodontal and cardiovascular disease

Periodontitis+Cardiovascular

Evaluation of ET-1 level and correlation of ET-1 levels with periodontal and cardiovascular disease

Observation

Intervention Type OTHER

Evaluation of ET-1 level and correlation of ET-1 levels with periodontal and cardiovascular disease

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Observation

Evaluation of ET-1 level and correlation of ET-1 levels with periodontal and cardiovascular disease

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Presence of at least 16 teeth
* 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 contraceptives
* 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.
Minimum Eligible Age

21 Years

Maximum Eligible Age

71 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

University of Messina

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Gaetano Isola, DDS, PhD

Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Giovanni Matarese

Role: STUDY_DIRECTOR

University of Messina

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

University of Messina

Messina, , Italy

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Italy

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

10-918-10

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.