Periodontitis. Chronic periodontitis
Conditions
Interventions
Intervention 1: Control Group (Scaling and Root Planing only): In the control group, patients will receive only standard non-surgical periodontal therapy consisting of scaling and root planing. All pr
Sponsors
Kerman University of Medical Sciences
Eligibility
Sex/Gender
All
Age
30 Years to 50 Years
Inclusion criteria
Inclusion criteria: Individuals aged 30–50 years. Presence of clinically evident gingival recession, with signs such as edema, gingival redness, and bleeding on probing observed during clinical examination. Presence of maxillary and mandibular anterior teeth(Teeth with extensive or inadequate restorations, as well as teeth with large carious lesions, will be excluded). Systemically healthy individuals with no systemic conditions affecting the immune system, such as diabetes or pregnancy.
Exclusion criteria
Exclusion criteria: use of mouthwash, antibiotics, anti-inflammatory drugs, or immunosuppressive medications within the 3 months prior to the beginning of the study. use of any fixed or removable dental appliances. periodontal treatment received during the past 3 months. history of severe fluoride hypersensitivity. use of medications that affect the periodontium, such as nifedipine, corticosteroids, etc. smokers and individuals who use tobacco. Presence of other gingival diseases (except periodontitis).
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Calculus level of patients. Timepoint: Before the intervention, 4 weeks after completion of the intervention, and 8 weeks after completion of the intervention. Method of measurement: Calculus Surface Index - CSI & Calculus Severity Surface Index - CSSI.;Gingival Inflammation. Timepoint: Before the intervention, 4 weeks after completion of the intervention, and 8 weeks after completion of the intervention. Method of measurement: Measured using the Loe & Silness Gingival Index. | — |
Secondary
| Measure | Time frame |
|---|---|
| Dental hypersensitivity of patients. Timepoint: Before the intervention, 4 weeks after completion of the intervention, and 8 weeks after completion of the intervention. Method of measurement: Measured for each tooth using the Visual Analogue Scale.;Clinical attachment level of patients. Timepoint: Before the intervention, 4 weeks after completion of the intervention, and 8 weeks after completion of the intervention. Method of measurement: Measured using a standardized periodontal probe recording the distance from Cementoenamel junction to periodontal papilla.;Dental staining of the four maxillary and mandibular anterior teeth. Timepoint: Before the intervention, 4 weeks after completion of the intervention, and 8 weeks after completion of the intervention. Method of measurement: modified Lobene index.;Dental plaque level of the four maxillary and mandibular anterior teeth. Timepoint: Before the intervention, 4 weeks after completion of the intervention, and 8 weeks after completion of the intervention. Method of measurement: sillness & Loe Plaque Index. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSajjad Pourmoshrefi
Kerman University of Medical Sciences
Outcome results
None listed