Tinder Fungus as an Adjunct to Non-surgical Periodontal Therapy for Periodontitis
Tinder Fungus (Fomes Fomentarius) as an Adjunct to Non-surgical Periodontal Therapy for Periodontitis: A Randomized Controlled Trial
1 other identifier
interventional
70
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Sep 2026
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 10, 2026
CompletedFirst Posted
Study publicly available on registry
March 19, 2026
CompletedStudy Start
First participant enrolled
September 1, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2027
Study Completion
Last participant's last visit for all outcomes
December 1, 2028
July 16, 2026
January 1, 2026
1.2 years
March 10, 2026
July 14, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Bleeding on probing (BoP in %) change
Bleeding on probing (BoP in %) changes from baseline (T0) to reevaluation (T1). BOP will be recorded as yes/no for each of 6 sites and reported as the percentage of affected sites per participant.
changes from baseline (T0; 1 day before intervention starts) to reevaluation (T1; 5 weeks (±1 week) after intervention start)
Study Arms (2)
Tinder fungus-based formulation (toothpaste and oral supplement powder)
EXPERIMENTALTinder fungus toothpaste plus oral supplement powder as adjuncts to non-surgical periodontal therapy (NSPT) in patients with periodontitis
commercially available toothpaste
ACTIVE COMPARATORCommercially available toothpaste as adjuncts to non-surgical periodontal therapy (NSPT) in patients with periodontitis
Interventions
Participants will receive Tinder fungus (Fomes fomentarius)-based formulations including a toothpaste plus an oral supplement powder as adjuncts to non-surgical periodontal therapy (NSPT).
A standard commercially available toothpaste administered as an adjunct to NSPT.
Eligibility Criteria
You may qualify if:
- 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
- Patients who are willing to use interdental brushes
You may not qualify if:
- 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)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Dental Clinic of the Sigmund Freud Private University
Vienna, State of Vienna, 1020, Austria
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 10, 2026
First Posted
March 19, 2026
Study Start (Estimated)
September 1, 2026
Primary Completion (Estimated)
December 1, 2027
Study Completion (Estimated)
December 1, 2028
Last Updated
July 16, 2026
Record last verified: 2026-01