About this trial
This study is a randomized, controlled, split-mouth clinical trial designed to evaluate and compare the effectiveness of four different subgingival adjuncts used along side standard Scaling and Root Planning (SRP). This protocol is designed to be a standardized therapeutic model. The subgingival adjuncts are standardized, ensuring that the results are not operator dependent and can be replicated across any dental unit. The primary goal of this study is to evaluate the clinical efficacy of three distinct adjunctive strategies: Biological (I-PRF), Antiseptic : Povidone- iodine , Diode-Laser activation, compared to a Saline Control in the initial treatment of stage 2, 3 and stage 4 of the 2018 AAP/EFP periodontal classification.
Eligibility criteria
Qualifiers
Pregnant /Lactating
History of radiotherapy or chemotherapy in the head/neck region.
Known hypersensitivity to Iodine or Methylene blue solution
Systematic antibiotic use within the last 30 days
Disqualifiers
None
Trial design
Treatments tested in this trial
- Injectable Platelet-Rich Fibrin (I-PRF)
- Diode Laser Activation
- Povidone-Iodine Irrigation (1%)
- Saline Irrigation (0.9%)
- Scaling and Root Planing