Comparing two surgical methods for treating periodontitis

Modified Widman Flap (MWF) vs Fibre Retention Osseous Resective Surgery (FibReORS): A Randomized, Controlled, Clinical Trial.

Not applicable Interventional University of Florence · NCT06123000

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

PhaseNot applicable
Study typeInterventional
Enrollment36 (estimated)
Ages18 Years and up
SexAll
SponsorUniversity of Florence Academic / other
Locations1 site (Florence, FI)
Trial IDNCT06123000 on ClinicalTrials.gov

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.

Who should consider this trial

Good fit: Ideal candidates are adults aged 18 and older with periodontitis and specific residual pockets that meet the study criteria.

Not a fit: Patients with severe periodontal conditions or those requiring extensive prior treatments may not benefit from this study.

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 performed: Previous studies have shown varying success with surgical interventions for periodontitis, but this specific comparison is novel.

Eligibility criteria

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 this trial is running

Florence, FI

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions PeriodontitisPeriodontal PocketPeriodontal Attachment Loss
Last reviewed 2026-06-09 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.