Actively Recruiting
Performance of the Treatment of Periodontitis According to the Bioperio® Protocol
Led by University of Pisa · Updated on 2026-05-01
5000
Participants Needed
1
Research Sites
365 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This multicenter, prospective, single-arm observational study evaluated the clinical performance of the Bioperio® protocol, a standardized, patient-centered framework for managing periodontitis. The protocol combined professional supra-gingival scaling, oral hygiene instruction and motivation, full-mouth subgingival instrumentation, and-in Stage III/IV cases-adjunctive enamel matrix derivative application in deep pockets.
CONDITIONS
Official Title
Performance of the Treatment of Periodontitis According to the Bioperio® Protocol
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Confirmed diagnosis of periodontitis (proximal attachment loss in 2 non-adjacent teeth)
- No previous treatment for periodontitis
- Systemically healthy or with well-controlled chronic medical conditions
- Willingness to participate in the study and comply with the follow-up schedule
You will not qualify if you...
- Pregnancy or breastfeeding
- Patients previously treated for periodontitis
- Poorly controlled systemic conditions
- Refusal to participate
- Patients who did not complete the proposed treatment plan
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Pisa
Pisa, None Selected, Italy, 56126
Actively Recruiting
Research Team
F
Filippo Graziani, Prof.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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