- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06835452
Comparison of Current Subgingival Debridement Methods
Comparison of Current Subgingival Debridement Methods: Clinical Trial with 6 Months Follow-up
Our study aimed to compare the effectiveness of current subgingival debridement methods used in the treatment of Stage 1 and Stage 2 periodontitis patients, the aesthetic condition achieved after these treatments, and the pain felt during treatment.
90 female patients who were diagnosed with chronic periodontitis (Stage 1-2) and required supra-subgingival scaling for treatment purposes, and who volunteered to participate in the study, were included in the study. Three treatment groups were determined. 30 people were included in each group. Periodontal examination was performed before and after the treatments in the 1st month, 3rd month and 6th month and the data on the collected periodontal parameters were analyzed.
Study Overview
Status
Detailed Description
Periodontal parametreler Gingival index, plaque index, periodontal pocket depth and bleeding index on probing.
It was evaluated with the visual analog scale for pain and aesthetics.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Niğde, Turkey
- Nigde Omer Halisdemir University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Systemically healthy patient (without known chronic disease)
- Periodontal diagnostic data (Gingival Index, Plaque Index, Periodontal pocket depths, Attachment loss, Radiological data-Bone loss data) are complete
- Treatments diagnosed with stage 1-2 periodontitis and those who have not had periodontal treatment in the last 6 months
Exclusion Criteria:
- Having a systemic disease
- Pregnant and lactating women
- smoker
- Those who do not want to participate in the study
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Group 1- classic treatment
Subgingival debridement was performed using the Cavitron and Gracey curette (this is the method that is used routinely).
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Group 2-Guided Biofilm Therapy
Subgingival debridement was performed with the Guided Biofilm Therapy (GBT+Airabrasion) method.
This method is the most up-to-date method.
The biofilm is shown to the patient with plate dye, and the biofilm is cleaned with air abrasion and perio flow (EMS device cavitron).
In the patient's control sessions, the patient's oral hygiene motivation is tried to be increased by dyeing the biofilm.
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Group 3- Classical treatment and with Plaque paint
the dental calculus and biofilm were stained with plaque paint, shown to the patient with the help of a mirror, and then routine subgingival debridement was performed.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Gingival index
Time Frame: baseline, 1st month, 3rd month and 6th month
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4 surfaces of all teeth (distal, buccal, mesial, lingual) are evaluated 0= Normal gingiva
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baseline, 1st month, 3rd month and 6th month
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Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2023/65
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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