Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT07013682

PRF as Adjunct to Subgingival Instrumentation in Step 2 Periodontal Therapy

Led by University of Bern · Updated on 2025-06-25

20

Participants Needed

1

Research Sites

86 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Periodontitis is characterized by a chronic, multifactorial inflammatory process driven by dysbiotic plaque biofilms. It is recognized as the most common chronic inflammatory non-communicable disease in humans. The advanced and severe forms of periodontitis have an estimated prevalence of 7.4%, while milder forms can affect up to 50% of the population. If left untreated, periodontitis can lead to tooth loss. However, it is largely preventable and treatable with mechanical non-surgical periodontal therapy. To improve periodontal healing and thus clinical attachment gain after non-surgical therapy, adjunctive bioactive formulations such as enamel matrix derivatives, sodium hypochlorite, locally delivered antimicrobials, or hyaluronic acid have recently been proposed. However, these agents are non-autologous formulations and expensive. Platelet-rich fibrin (PRF) acts as a scaffold that inhibits the early migration of epithelial cells into the periodontal tissues. Its regenerative properties are primarily due to its ability to promote angiogenesis. This ability is attributed to the 3D fibrin matrix, which can simultaneously transport several cytokines and growth factors. These include vascular endothelial growth factor (VEGF), insulin growth factor (IGF), transforming growth factor β1 (TGF-β1) and platelet-derived growth factor (PDGF). PRF further shows antibacterial properties and accelerates soft tissue healing. So far PRF is not routinely used in periodontal non-surgical therapy. The aim of this 6-month, split-mouth randomized clinical trial including 20 patients is to test whether PRF can improve the results after non-surgical therapy.

CONDITIONS

Official Title

PRF as Adjunct to Subgingival Instrumentation in Step 2 Periodontal Therapy

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Men and women aged 65 18 years
  • Diagnosed with generalized periodontitis stage II-IV, grade A/B/C
  • Have at least 20 natural teeth (excluding wisdom teeth)
  • Do not have removable dentures
  • Willing to provide written informed consent and complete the 6-month follow-up
Not Eligible

You will not qualify if you...

  • Currently participating in other clinical trials
  • Received periodontal treatment in the previous 12 months
  • Taken antibiotics within 3 months before study entry
  • Require antibiotic prophylaxis for dental treatment
  • Using medications that may affect periodontitis clinical features
  • Pregnant or lactating
  • Have any condition preventing venipuncture or unwilling to have blood drawn
  • Currently undergoing cancer treatment
  • History of radiation therapy in the head or neck area

AI-Screening

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Trial Site Locations

Total: 1 location

1

Department of Periodontology, University of Bern

Bern, Switzerland, 3010

Actively Recruiting

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Research Team

A

Alexandra Stähli, DMD

CONTACT

J

Jean-Claude Imber, DMD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

2

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PRF as Adjunct to Subgingival Instrumentation in Step 2 Periodontal Therapy | DecenTrialz