Active (not recruiting)
Not applicable
NCT07540624
Efficacy of Chlorhexidine and Morus Nigra Mouthwashes After Periodontal Treatment
No applicable phase (e.g. observational)
Conditions:
Periodontitis
Periodontal Disease
Sponsor: Inonu University
trial.available_in:
БГ
Overview
This study aims to evaluate and compare the clinical, biochemical, and microbiological effects of chlorhexidine and Morus nigra (blackberry) mouthwashes used as an adjunct to non-surgical periodontal treatment (scaling and root planing - SRP) in patients with periodontal diseases. The participants will be divided into three groups: a control group receiving only SRP, a group receiving SRP combined with chlorhexidine mouthwash, and a group receiving SRP combined with Morus nigra mouthwash. Clinical periodontal parameters, gingival crevicular fluid levels of inflammatory markers (including TNF-a, IL-1b, and IL-10), and subgingival plaque microbiological profiles (such as red complex bacteria and Fusobacterium) will be evaluated at baseline, 1 month, and 3 months after the treatment.
Who can participate
Inclusion Criteria:
* Patients diagnosed with periodontitis.
* Systemically healthy individuals.
* Patients aged between 18 and 65 years.
* Presence of at least 20 natural teeth.
* Volunteering to participate in the study and signing the informed consent form.
Exclusion Criteria:
* Presence of any systemic disease that may affect periodontal health or systemic inflammatory response (e.g., Diabetes Mellitus, immunological disorders).
* Current smokers or use of any tobacco products.
* Pregnancy or lactation.
* Use of systemic antibiotics, anti-inflammatory drugs, or immunosuppressive medications within the last 6 months.
* Having received any non-surgical or surgical periodontal treatment within the last 6 months.
* Known allergy or sensitivity to chlorhexidine or Morus nigra (blackberry) extracts.
* Patients using orthodontic appliances.