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
1057 participants
OBSERVATIONAL
2020-06-01
2022-06-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Study Groups
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Periodontal examination
Cross- sectional clinical periodontal examinations and measurements were performed using a Williams periodontal probe
Clinical examination
A total of 1057 individuals who applied to Bolu Abant İzzet Baysal University, Faculty of Dentistry, Department of Periodontology and agreed to participate in the study were clinically and radiologically examined.
An intraoral scanner was utilized to capture direct optical intraoral data of a patient.
Interventions
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Clinical examination
A total of 1057 individuals who applied to Bolu Abant İzzet Baysal University, Faculty of Dentistry, Department of Periodontology and agreed to participate in the study were clinically and radiologically examined.
An intraoral scanner was utilized to capture direct optical intraoral data of a patient.
Eligibility Criteria
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Inclusion Criteria
* Periodontal status ranging from no clinical periodontal disease (\<10% with bleeding on probing) to periodontitis (stage I to IV)
* Patients having at least one teeth in each quadrant were included.
Exclusion Criteria
18 Years
ALL
Yes
Sponsors
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Abant Izzet Baysal University
OTHER
Istanbul Technical University
OTHER
The Scientific and Technological Research Council of Turkey
OTHER
Bezmialem Vakif University
OTHER
Responsible Party
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Şadiye GÜNPINAR
Principal Investigator
Principal Investigators
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Şadiye Günpınar, Assoc. Prof
Role: PRINCIPAL_INVESTIGATOR
Bezmialem Vakif University
Locations
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Bezmialem Vakif University
Istanbul, , Turkey (Türkiye)
Countries
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Other Identifiers
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119S025
Identifier Type: -
Identifier Source: org_study_id
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