Evaluation of the Effect of Streptococcus Salivarius K12 Probiotic in the Treatment of Periodontitis
- Conditions
- Periodontitis Stage IIIProbiotic
- Registration Number
- NCT06871540
- Lead Sponsor
- AYŞENUR ŞAHİN
- Brief Summary
Aims: The use of oral probiotics as an adjunct to the treatment of periodontal diseases is known to be beneficial in antagonizing pathogenic microflora and regulating the host immune response. The aim of this clinical study was to evaluate the clinical, microbiologic and biochemical effect of Streptococcus salivarius (S. salivarius) K12 probiotic tablet as an adjunct to scaling and root planing (SRP) treatment in stage 3 periodontitis patients.
Methods: The study included 30 systemically healthy stage 3 periodontitis patients. After non-surgical periodontal treatment, participants were randomly assigned to the test (SRP+Probiotic, n=15) or control (SRP, n=15) group. Patients in the test group used probiotic tablets once daily for 30 days. Clinical (Plaque index (PI), gingival index (GI), bleeding on probing (BOP), probing depth (PD), clinical attachment level (CAL)), microbiological (Porphyromonas gingivalis, Treponema denticola, Tannerella forsythia, Prevotella intermedia, Aggregatibacter actinomycetemcomitans, Fusobacterium nucleatum) and biochemical (IL-6, IL-8, IL-10) measurements were performed at baseline (before SRP), 30. and 90th days. Data were analyzed statistically.
Keywords: Microbiology, Periodontitis, Probiotics, Cytokines
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 30
- Male or female aged 18-60 years,
- No systemic disease,
- No periodontal treatment in the last 6 months,
- No antibiotic therapy in the last 6 months,
- Diagnosed with stage 3 periodontitis according to the 2017 periodontal disease classification
- Periodontal treatment within sixteen months,
- Smoking,
- Patients with systemic health problems such as diabetes, rheumatoid arthritis, neurological diseases, lung and kidney diseases,
- Pregnancy or lactation,
- Acute oral lesions or necrotizing ulcerative periodontitis.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Reduction in Porphyromonas gingivalis at 3 months From enrollment to the end of treatment at 12 weeks
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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Trial Locations
- Locations (1)
İnönü Üniversitesi Diş Hekimliği Fakültesi
🇹🇷Malatya, Battalgazi, Turkey
İnönü Üniversitesi Diş Hekimliği Fakültesi🇹🇷Malatya, Battalgazi, Turkey