Comparing two surgical methods for treating periodontitis
Official title: Modified Widman Flap (MWF) vs Fibre Retention Osseous Resective Surgery (FibReORS): A Randomized, Controlled, Clinical Trial.
Run by University of Florence · NCT06123000 · Data updated 2026-11-12
This study tests which of two surgical methods works better for people with periodontitis who still have deep pockets around their teeth after initial treatment.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 36 (estimated) |
| Sponsor | University of Florence Academic / other |
| Locations | 1 site (Florence, FI) |
| Status | Recruiting |
| Started | October 21, 2024 |
| Main results expected | October 21, 2025 |
| Study ends | October 21, 2026 |
| Registry record updated | April 10, 2025 |
| Trial ID | NCT06123000 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults aged 18 and older with periodontitis and specific residual pockets that meet the study criteria.
✕Probably not a fit
Patients with severe periodontal conditions or those requiring extensive prior treatments may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This clinical trial evaluates the effectiveness of two surgical approaches, Modified Widman Flap and Fiber Retention Osseous Resective Surgery, in treating periodontitis. The study focuses on patients with residual periodontal pockets after initial treatment steps, aiming to reduce the risk of disease progression and tooth loss. Participants will undergo one of the two surgical interventions to assess which method yields better outcomes in terms of pocket depth and overall periodontal health.
Why it matters
Potential benefit: If successful, this study could lead to improved surgical techniques for managing periodontitis, potentially reducing tooth loss and enhancing oral health.
How similar studies have gone: Previous studies have shown varying success with surgical interventions for periodontitis, but this specific comparison is novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age ≥ 18 years; * Patients affected by periodontitis; * No systemic disease or pregnancy; * No systemic antibiotic therapy in 6 months preceding the enrollment; * Smoking ≤ 20 cigarettes/day; * Full-mouth plaque score (FMPS) and full- mouth bleeding score (FMBS) ≤ 15%; * Residual periodontal pocket ≥5 mm with bleeding on probing at posterior natural teeth; * Experimental pocket associated with a detectable infrabony defect ≤ 3mm at x-ray; * No history of periodontal surgery at the experimental site. Exclusion Criteria: * Undetectable cemento-enamel junction (CEJ) at experimental teeth; * Severe furcation involvement (class II and III); * Abutment for prosthetic rehabilitation; * Periodontal Pockets associated with infrabony defect \>3 mm; * Horizontal bone loss higher than 1/3 of the root length at experimental teeth; * Severe tooth mobility at baseline (class 2 or 3).
Where it's running
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Università degli Studi di Firenze
Florence, Fi, Italy Recruiting
Study contacts
- Study coordinator: Luigi Barbato, Dr.
- Email: luigi.barbato@unifi.it
- Phone: 3299457556
Similar studies
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.