Fractal Analysis Method in Periodontal Disease

NCT ID: NCT05639582

Last Updated: 2022-12-08

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

Clinical Phase

NA

Total Enrollment

200 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-11-05

Study Completion Date

2021-11-05

Brief Summary

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

In this study, the effects of periodontal disease on alveolar bone were investigated using fractal analysis method.

Detailed Description

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

Background: It is very difficult to objectively evaluate the negative changes in bone structure due to periodontitis. The present study was aimed to evaluate the trabecular bone changes between healthy individuals and periodontitis patients by fractal dimension analysis on digital panoramic radiographs.

Method: The study included 50 periodontally healthy individuals (control group), 50 individuals with Stage 1 periodontitis (S1-P group), 50 individuals with Stage 2 periodontitis (S2-P), and 50 individuals with Stage 3 periodontitis (S3-P), a total of 200 individuals were included. The fractal dimension (FD) value of the trabecular bone in the interproximal space between mandibular first molar and second premolar tooth roots was evaluated using Image J program. The mean fractal dimension values of the two regions were calculated by box counting method.

Conditions

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

Periodontal Diseases

Study Design

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

Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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

periodontally healthy individuals

50 subject without any periodontal disease

Group Type EXPERIMENTAL

fractal analysis

Intervention Type OTHER

fractal analysis is a method that numerically expresses bone changes.

Stage 1 periodontitis

50 subject diagnosed with stage 1 in the periodontal disease classification

Group Type EXPERIMENTAL

fractal analysis

Intervention Type OTHER

fractal analysis is a method that numerically expresses bone changes.

Stage 2 periodontitis

50 subject diagnosed with stage 2 in the periodontal disease classification

Group Type EXPERIMENTAL

fractal analysis

Intervention Type OTHER

fractal analysis is a method that numerically expresses bone changes.

Stage 3 periodontitis

50 subject diagnosed with stage 3 in the periodontal disease classification

Group Type EXPERIMENTAL

fractal analysis

Intervention Type OTHER

fractal analysis is a method that numerically expresses bone changes.

Interventions

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

fractal analysis

fractal analysis is a method that numerically expresses bone changes.

Intervention Type OTHER

Eligibility Criteria

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

Inclusion Criteria

* 18-65 years old
* Getting a diagnosis of stage 1,2 and 3 periodontitis
* Be diagnosed as periodontally healthy
* Have no barriers to obtaining radiographs
* Not having any systemic disease that may affect periodontal status
* Not smoking and alcohol use
* Volunteer to participate in the study

Exclusion Criteria

* Those who use drugs that can affect bone metabolism
* Radiographs with poor diagnostic quality
* Root canal treatment or teeth with periapical lesions in the area of interest
* Individuals who have suffered a fracture or trauma that affects the anatomy or integrity
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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

Necmettin Erbakan University

OTHER

Sponsor Role lead

Responsible Party

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

Ummuhan Tekin Atay

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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

Necmettin Erbakan University

Konya, , Turkey (Türkiye)

Site Status

Countries

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

Turkey (Türkiye)

Other Identifiers

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

Ummuhantekinatay

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

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