Periodontitis Clinical Trial
Official title:
Effects of Nd:YAG Laser and Air Abrasive Combined Application on Clinical Parameters in Addition to Non Surgical Periodontal Treatment in Patients With Periodontitis
Verified date | October 2021 |
Source | Izmir Katip Celebi University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The aim of this clinical study is to investigate the effectiveness of the combined application of Nd:YAG (neodymium-doped yttrium aluminum garnet) laser and air abrasive applied in addition to nonsurgical periodontal treatment on clinical parameters in patients with periodontitis. A split-mouth, randomized study included 24 systemically healthy, non-smoker, periodontitis patients. In addition to non-surgical periodontal treatment, air abrasive (erythritol-chlorhexidine powder) and Nd:YAG laser (2 W, 200mJ, 10 Hz) combined application was applied to the test group, while only non-surgical periodontal treatment was applied to the control group. Clinical periodontal records of the patients, including plaque index (PI), gingival index (GI), bleeding on probing (BOP), probing pocket depth (PD), clinical attachment level (CAL), were taken before the treatment and at the 1st and 3rd months after the treatment. All clinical parameters improved significantly from baseline for both groups after treatment (p˂0.05). In the evaluation between the test and control groups, no statistically significant difference was found in the PI, GI and BOP parameters of the patients at any time (p˃0.05). While the amount of change in PD and CAL values after treatment in medium deep pockets in the study groups was compared, no significant difference was observed between the groups (p˃0.05), statistically significant improvements in PD and CAL parameters were observed in the test group compared to the control group only for deep pockets (≥7 mm) among the groups (p˂0.05).In conclusion, it has been observed that the combined application of Nd:YAG laser and air abrasive in systemically healthy, stage III and grade C periodontitis patients is in the short term on PD and CAL, especially in inaccessible areas such as deep pockets.
Status | Completed |
Enrollment | 24 |
Est. completion date | September 1, 2020 |
Est. primary completion date | September 1, 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 20 Years to 70 Years |
Eligibility | Inclusion Criteria: - Systemically healthy (The determination of healthy volunteers will be based on the statements of the patients in the anamnesis. No additional examinations will be made.), - Having a total of at least twenty permanent teeth in the mouth, - Non-smoker - Have not used antibiotics, anti-inflammatory and systemic corticosteroid drugs in the last 6 months, - Not in pregnancy or lactation period, - Patients who have not received periodontal treatment in the last 6 months, - Patients who accepted the research and signed the informed volunteer consent form - Bleeding on probing in 30% or more areas, - 5 mm or more probing pocket depth in each quadrant in at least 2 non-adjacent teeth - 4mm or more attachment loss, - Coronal 1/3 or more (horizontal and/or vertical) on radiograph individuals with bone loss were included Exclusion Criteria: - Having any systemic disease, - Regularly using a systemic medication, - Being pregnant or lactating. - To have had periodontal treatment in the last 6 months. - Receiving antibiotic, anti-inflammatory or systemic corticosteroid medication in the last 6 months. - Smoking. |
Country | Name | City | State |
---|---|---|---|
Turkey | Izmir Katip Celebi University Faculty of Dentistry | Izmir | Çigli |
Lead Sponsor | Collaborator |
---|---|
Izmir Katip Celebi University |
Turkey,
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* Note: There are 14 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Clinical attachment level change | With the help of a Williams periodontal probe, the distance between the enamel-cementum border and the sulcus/pocket floor will be measured from the six points of the tooth: mesiobuccal, midbuccal, distobuccal, mesiopalatal/lingual, mid-buccal/palatal and distobuccal/palatal. | Change from baseline clinical attachment level at 3 months |
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