Clinical Effectiveness of Biologic Agents as an Adjunct to Non-surgical Periodontal Therapy of Intrabony Defects

Recruiting N/A Interventional Study
Periodontal Diseases Periodontal Attachment Loss Pocket, Periodontal Intrabony Periodontal Defect
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
88 (estimated)
Sponsor
G. d'Annunzio University · Other
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About This Trial
The aim of the present study is to clinically and radiographically compare the efficacy of recombinant human platelet-derived growth factor (rhPDGF), Leukocyte-Platelet Rich Fibrin (L-PRF) and Enamel Matrix Derivatives (EMD) in intrabony defects following minimally invasive non surgical peridoontal therapy (MINST). This study will be designed as a randomized clinical trial of 12-month duration. A…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patients with a diagnosis of periodontitis stage III or IV (grades A to C), * non-smokers or former smokers who quit at least 1 year ago, and * had not received any periodontal treatment in the 3 months prior to recruitment; * Presence of at least 1 Infrabony defect (PPD ≥ 5 m…
Contacts

Michele Paolantonio, DDS, MD

3395204073

michelepaolantonio@gmail.com

CONTACT