Reconstructive Treatment of Peri-implantitis With Combined Defects

Recruiting N/A Interventional Study
Peri-implantitis
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
18 – 75
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
60 (estimated)
Sponsor
Gazi University · Other
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About This Trial
The aim of this randomized clinical study is to assess the additional clinical benefit of incorporating a resorbable collagen membrane (CM) alongside a xenogeneic bone graft-specifically, deproteinized bovine bone mineral with 10% collagen (DBBM-C)-in the reconstructive surgical treatment of peri-implantitis involving combined (i.e., contained and non-contained) defect configurations. Accordingly…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Peri-implantitis defined as the presence of a peri-implant probing pocket depth (PPD) ≥6 mm with bleeding and/or suppuration on probing (BoP/SoP) and radiographic marginal bone loss (MBL) ≥3 mm. * Presence of combined defect configuration Class \[Ib, Ic, Ie with horizontal com…
Contacts

Sila Cagri Isler, PhD

+905069966074

silaisler@gazi.edu.tr

CONTACT