About this trial
The goal of this interventional clinical study is to learn if a Tinder fungus-based formulation -specifically a toothpaste and oral supplement powder-works as adjuncts to non-surgical periodontal therapy (NSPT) in patients with periodontitis.
The main questions it aims to answer is:
• Does the Tinder fungus-based formulation as an adjunct to NSPT reduce bleeding on probing more than a commercially available toothpaste as an adjunct to NSPT? Researchers will compare tinder fungus toothpaste and oral powder as an adjunct to NSPT to a commercially available toothpaste as an adjunct to NSPT to see if the Tinder fungus-based formulation works as adjuncts to NSPT in patients with periodontitis.
Participants will:
* Take tinder fungus toothpaste and oral powder or a commercially available toothpaste as an adjunct to NSPT twice daily for 30 consecutive days * Visit the clinic at least twice including a visit before and after the intervention * Keep a diary documenting their well-being and the number of times they used the toothpastes in the morning and evening.
Eligibility criteria
Qualifiers
Patients diagnosed with Stage III or IV periodontitis
Patients who have not yet initiated periodontal therapy
Patients who have at least 20 remaining teeth
Patients who are willing to use an electric toothbrush
Disqualifiers
Patients who have previously received treatment for periodontitis
Patients who have already undergone or initiated periodontal therapy
Patients with a known allergy or intolerance to any component of the toothpaste or the powder
Patients who are already using a product that contains tinder fungus (Fomes fomentarius)
Trial design
Treatments tested in this trial
- Tinder fungus-based formulation
- Commercially available toothpaste