Regular Home-use of Dual-light Photodynamic Therapy in the Management of Chronic Stage III-IV Periodontitis
Periodontitis Chronic Generalized Moderate, Periodontitis Chronic Generalized Severe
About this trial
This is an interventional treatment trial for Periodontitis Chronic Generalized Moderate focused on measuring Lumoral, Lumorinse, Periodontitis, Anti-bacterial photodynamic therapy, aPDT, Plaque, aMMP-8, Photobiomodulation
Eligibility Criteria
Inclusion Criteria: Periodontal disease stage III-IV, according to criteria the American Academy of Periodontology (AAP) with at least 3 mm interdental clinical attachment level (CAL) in the site of greatest loss. ≥ 18 years old Presence of ≥20 teeth, including implants Agreement to participate in the study and to sign a written consent form Able to co-operate with the treatment protocol and avoid any other oral hygiene measures outside of the study protocol Exclusion Criteria: Grade A or C periodontitis Presence of any physical limitation or restriction that might restrict Lumoral use Pregnancy or lactation Active smoking Medicated diabetes mellitus (DM) Any systemic disease (e.g., wound healing dysfunctions) that could alter the progression of periodontal disease Use of antibiotics within 4 weeks week prior study Periodontal treatment within 3 months prior study Removable major prosthesis or major orthodontic appliance A need for a hopeless teeth extraction, or open cavities in need for immediate endodontic treatment
Sites / Locations
- Hospital of Lithuanian University of Health Sciences Kaunas Clinics, Department of Dental and Oral PathologyRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Study group
Control group
A complete clinical intraoral examination shall be performed for all subjects. Same demographic and clinical data will be obtained from subjects in both arms. The study group shall receive the Lumoral treatment -device, Lumorinse -tablets and instructions for their use. All subjects shall receive standard oral hygiene instructions for the use of an electric toothbrush, interdental brush, and dental floss.
A complete clinical intraoral examination shall be performed for all subjects. Same demographic and clinical data will be obtained from subjects in both arms. All subjects shall receive standard oral hygiene instructions for the use of an electric toothbrush, interdental brush, and dental floss.