Necmettin Erbakan University Faculty of Dentistry, Department of Periodontology, Konya, Turkey
Konya, Turkey (Türkiye)
Location status: Recruiting
NCT Number: NCT07327658
This study is a prospective, observational clinical research conducted at the Department of Periodontology, Faculty of Dentistry, Necmettin Erbakan University. The study aims to evaluate periodontal records routinely obtained before treatment and throughout the treatment process from individuals who visited the clinic and were planned for non-surgical periodontal treatment. Within the scope of the research, the effectiveness of periodontal treatments will be evaluated solely through non-invasive clinical periodontal parameters. No additional invasive procedures will be performed during the study; only records obtained during routine periodontal examinations and treatments at the clinic will be used.
Interested in participating?
Request Info18 year–65 year
All sexes
Interventional
Not applicable
Konya, Turkey (Türkiye)
Location status: Recruiting
Patient Selection:
The study will include individuals aged 18-65 who have been diagnosed with periodontitis. All patients' treatment processes will be carried out within the framework of standard protocols implemented at our clinic, and patients will be called for regular follow-up appointments scheduled between 1 month and 1 year after treatment. Data from patients with a 6-month follow-up period will be evaluated within the scope of the study.
Inclusion criteria
Exclusion criteria
Clinical Periodontal Examination and Measurements:
All individuals participating in the study undergo routine clinical and radiographic evaluations before and during treatment. The parameters measured during periodontal examinations are as follows:
Patients' sociodemographic data and oral hygiene habits are also recorded. Periodontal disease diagnosis and classification are performed according to the 2017 Classification of Periodontal and Peri-Implant Diseases and Conditions criteria.
Stage 3 periodontitis: 25 individuals Stage 4 periodontitis: 25 individuals
Application Principle of the Study:
No additional interventional procedures will be performed on individuals within the scope of this study; records obtained during routine treatments at the clinic will be used. The effectiveness of periodontal treatments will be evaluated by comparing clinical measurements obtained before periodontal treatment and during follow-up sessions. The main objective of the study is to demonstrate the effectiveness of non-surgical periodontal treatment protocols through the analysis of clinical records.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Periodontal treatment was performed according to standard clinical protocols. Periodontal pocket depth was measured at baseline and at 1, 3, and 6 months following treatment.
Time frame: Baseline, 1 month, 3 months, and 6 months
Contact information is provided by the study sponsor or research team.
Necmettin Erbakan University
Other
Investigation of the Changes in Periodontal Pocket Depth Following Periodontal Treatment in Patients With Periodontitis
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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