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
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
4965 participants
OBSERVATIONAL
2018-02-02
2023-09-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Identification of EMT Indicators in Healthy and Periodontally Diseased Gingival Samples
NCT03462953
Tissue Alterations in Aggressive and Chronic Periodontitis
NCT03625414
Dietary Intakes and Periodontal Outcomes After Sanative Therapy
NCT02291835
Tooth Loss Rate and Its Associated Factors: a Retrospective Cross-sectional Study With up to 50 Years of Follow-up.
NCT06578806
The Link Between Periodontitis, Smoking and Oral Cancer
NCT04047212
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
1. Periodontally healthy patients: Patients with a D1110 or D1111 (adult prophylaxis including those with 6 or fewer teeth) treatment code, seen by a 3rd or 4th year pre-doctoral dental student. Excludes all charts that have ever had a U4990 (Perio case) treatment code. Patient is 35 years or older relative to 1/1/2016.
2. Patients with a history of advanced periodontal treatment, group 1: All patients treated in the Postgraduate Periodontics department by a periodontics resident between 1/1/2000 - 12/31/2017. Patients presenting for treatment of chronic periodontitis will be included while those patients presenting to the clinic for other reasons, such as crown lengthening procedures, will be labeled as such. All patients selected will be 35 years or older at time of initial exam.
3. Patients with history of advanced periodontal treatment, group 2: All patients ever treated in the private faculty practice of one periodontist, that were still active patients during between 1/1/16 - 12/31/16. Only those 35 years and older were included. Patients presenting for treatment of chronic periodontitis will be included while those patients presenting to the clinic for other reasons, such as crown lengthening procedures, will be labeled as such.
All duplicates within a group will be excluded (e.g. patients may have had a D1110 code more than once per year). These 3 subject search criteria should yield a sufficient number of patient records for statistical analysis.
All patient records will be reviewed and data will be collected and recorded in an electronic Microsoft Excel database file that is saved on an encrypted flash drive. The only patient identifier recorded will be the patient records number. Once data collection is complete, or at a maximum of 3 years from the start of the study, all identifying information will be deleted and only de-identified data saved on a separate electronic file will be analyzed. No code key will be required.
Data will be analyzed using ANOVA (F-test). If multiple variables are used, analysis will be by using generalized estimating equations (GEE).
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
OTHER
RETROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Periodontally healthy patients
Patients that have no history of periodontal treatment and that have been scheduled for routine prophylaxis appointments in the predoctoral clinics at the School of Dental Medicine, University at Buffalo.
NO intervention, patient records review only
There is no intervention - the three study groups are created by utilizing three unique sets of search criteria for the patient records review.
Periodontitis, group 1
Patients that have been referred from the pre-doctoral dental clinics to the Postgraduate Periodontics clinic for advanced periodontal disease. Clinical attachment loss, pain, mobility, bleeding, suppuration, and probing depths \> 4 mm more likely to be prevalent.
NO intervention, patient records review only
There is no intervention - the three study groups are created by utilizing three unique sets of search criteria for the patient records review.
Periodontitis, group 2
Patients referred to a faculty practice periodontist over the course of his clinical career due to chronic periodontitis that could not be treated by the referring general dentist. Clinical attachment loss, pain, mobility, bleeding, suppuration, and probing depths \> 4 mm more likely to be prevalent.
NO intervention, patient records review only
There is no intervention - the three study groups are created by utilizing three unique sets of search criteria for the patient records review.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
NO intervention, patient records review only
There is no intervention - the three study groups are created by utilizing three unique sets of search criteria for the patient records review.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* The remaining eligibility criteria varies between the three distinct subject populations, which are noted below. All eligibility criteria is selected for by an electronic search of patient records performed by the IT Department at the School of Dental Medicine, University at Buffalo.
1. Periodontally healthy patients:
1. A treatment code of D1110 or D111 was processed at least once but excluding patients that were ever assigned a treatment code of U4990
2. A 3rd or 4th year pre-doctoral dental student provider
3. 35 years or older as of 1/1/2016
4. Patient presented to clinic between 1/1/2016-12/31/2016
2. Patients with history of advanced periodontal treatment, group 1:
1. All patients presenting to the Postgraduate Periodontics Department at UB and being seen by a periodontics resident
2. Time period between 1/1/2000-12/31/2017
3. Patients will be 35 years or older at time of initial exam
4. Patients presenting for reasons other than chronic periodontitis treatment (e.g. crown lengthening) will be labeled as such.
3. Patients with history of advanced periodontal treatment, group 2:
1. All patients treated in the faculty practice of one periodontist that remained active patients during the time period 1/1/2016-12/31-2016
2. All patients were 35 years or older at time of initial exam
Duplicates within groups are eliminated.
Exclusion Criteria
Note: the majority of patient records selected by the search criteria done electronically by the IT department will be included in the study, since the search criteria very closely overlaps the overall study criteria
35 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University at Buffalo
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Dr. Lisa Yerke
Clinical Associate Professor, Department of Periodontics and Endodontics
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
School of Dental Medicine, University at Buffalo
Buffalo, New York, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
STUDY00001811
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.